Frailty, Fitness, and Quality of Life Outcomes of a Healthy and Productive Aging Program (GrandMove) for Older Adults With Frailty or Prefrailty: Cluster Randomized Controlled Trial

Introduction

Frailty, a common condition that increases with age, is a dynamic clinical state that can improve or worsen over time [Fried LP, Tangen CM, Walston J, et al. Frailty in older adults: evidence for a phenotype. J Gerontol A Biol Sci Med Sci. Mar 2001;56(3):M146-M156. [CrossRef] [Medline]1,Morley JE, Malmstrom TK, Miller DK. A simple frailty questionnaire (FRAIL) predicts outcomes in middle aged African Americans. J Nutr Health Aging. Jul 2012;16(7):601-608. [CrossRef] [Medline]2]. About 1 in 10 older adults are frail and 46% are prefrail, a state with higher risk of progression to frailty [O’Caoimh R, Sezgin D, O’Donovan MR, et al. Prevalence of frailty in 62 countries across the world: a systematic review and meta-analysis of population-level studies. Age Ageing. Jan 8, 2021;50(1):96-104. [CrossRef] [Medline]3]. Frailty is known to predict disability, mortality, risk of fractures, and many other adverse health outcomes [Vermeiren S, Vella-Azzopardi R, Beckwée D, et al. Frailty and the prediction of negative health outcomes: a meta-analysis. J Am Med Dir Assoc. Dec 1, 2016;17(12):1163. [CrossRef] [Medline]4]. To date, evidence for the management of frailty is the strongest with physical activity [Merchant RA, Morley JE, Izquierdo M. Editorial: Exercise, aging and frailty: guidelines for increasing function. J Nutr Health Aging. 2021;25(4):405-409. [CrossRef] [Medline]5,Travers J, Romero-Ortuno R, Bailey J, Cooney MT. Delaying and reversing frailty: a systematic review of primary care interventions. Br J Gen Pract. Jan 2019;69(678):e61-e69. [CrossRef] [Medline]6]. In older adults who are very frail, even small gains in strength can result in important functioning benefits and promote independence [Merchant RA, Morley JE, Izquierdo M. Editorial: Exercise, aging and frailty: guidelines for increasing function. J Nutr Health Aging. 2021;25(4):405-409. [CrossRef] [Medline]5]. Evidence suggested superior outcomes with training carried out 3 or more times per week, for 30-45 minutes per session, and lasting at least 3-5 months [2018 Physical Activity Guidelines Advisory Committee scientific report. Office of Disease Prevention and Health Promotion. 2018. URL: https://health.gov/sites/default/files/2019-09/PAG_Advisory_Committee_Report.pdf [Accessed 2025-04-30] 7]. Adherence to exercise training is good even in older adults with frailty, with few adverse events or safety concerns [Merchant RA, Morley JE, Izquierdo M. Editorial: Exercise, aging and frailty: guidelines for increasing function. J Nutr Health Aging. 2021;25(4):405-409. [CrossRef] [Medline]5].

Practice guidelines widely recommend multicomponent exercise programs for the management of frailty [Izquierdo M, Merchant RA, Morley JE, et al. International exercise recommendations in older adults (ICFSR): expert consensus guidelines. J Nutr Health Aging. 2021;25(7):824-853. [CrossRef] [Medline]8]. Many programs concurrently prescribe multimodal exercise components, even though sequential prescription may promote adherence and minimize attrition [Izquierdo M, Merchant RA, Morley JE, et al. International exercise recommendations in older adults (ICFSR): expert consensus guidelines. J Nutr Health Aging. 2021;25(7):824-853. [CrossRef] [Medline]8,de Labra C, Guimaraes-Pinheiro C, Maseda A, Lorenzo T, Millán-Calenti JC. Effects of physical exercise interventions in frail older adults: a systematic review of randomized controlled trials. BMC Geriatr. Dec 2, 2015;15(154):154. [CrossRef] [Medline]9]. The optimal sequence is yet to be investigated. Theoretically, strength and aerobic training contribute in different ways by slowing or compensating for muscle wasting and loss of endurance, as well as preventing other diseases and resisting the cascade of disability [Tseng BS, Marsh DR, Hamilton MT, Booth FW. Strength and aerobic training attenuate muscle wasting and improve resistance to the development of disability with aging. J Gerontol A Biol Sci Med Sci. Nov 1995;50 Spec No:113-119. [CrossRef] [Medline]10]. These exercise modalities impact on the older person’s quality of life by affecting their ability to lift load (eg, arising from a chair) and endurance in performing activities of daily living (eg, walking), allowing them to take control and lead a purposeful life. These may have implications for the design of exercise training protocols for frailty intervention.

Past development of exercise programs put a greater emphasis on maximizing physical benefits, while less focus was put on the scalability and sustainability of the program. It is foreseeable that the health care manpower gap as a result of population aging is increasing [Report of the strategic review on healthcare manpower planning and professional development. Health Bureau. 2017. URL: https://www.healthbureau.gov.hk/en/press_and_publications/otherinfo/180500_sr/srreport.html [Accessed 2025-04-30] 11] and heavy reliance on professionally led formal health care services for addressing frailty is unviable and unsustainable. Our team developed a multicomponent exercise program, namely the GrandMove program, which has a group of trained coaches in their 50s to 60s deliver the interventions. Delivery of exercise interventions by peer coaches rather than health professionals is a key to the long-term scalability and sustainability of such programs in the context of population aging. Our program incorporated both healthy and productive aging strategies. Although the program had clear goals of improving frailty, fitness, and quality of life in older adults with frailty and prefrailty, our peer coaches took on their own path to successful aging by adopting an active lifestyle and engaging in postretirement paid work. A detailed description of the program design is provided in the Methods and

Multimedia Appendix 1

Program design.

In this study, three intervention sequences were designed to (1) examine the effectiveness of a 6-month aerobic or resistance training program compared with lifestyle education as the active control intervention at 6 months, (2) investigate any order effect in resistance and aerobic training in older adults with frailty and prefrailty at 12 months, and (3) evaluate exercise habit formation over 18 months.

Methods

Study Design and Participants

This is an 18-month, multicenter, cluster randomized controlled trial with 3 intervention arms. A cluster design was used because of the logistical issues associated with the implementation of the interventions. The study sites included 14 community service centers for older adults and 15 public rental estates in Hong Kong. The staff from the participating sites referred potential participants based on their age and frailty status at screening.

Ethical Considerations

Designated research assistants, who were not involved in the intervention, obtained written informed consent and conducted screening interviews with the participants. The study protocol was approved by the institutional ethics committee (reference number EA1511048). The study was registered with the HKU Clinical Trials Registry (reference number HKUCTR-1964). All data used in this study were deidentified before analysis. Participants did not receive any compensation for their involvement.

Participants

Target study participants were older adults living in the community who did not have any contradictions to participation in a moderate level of physical activity. Between February 2016 and May 2017, older adults were invited to take part in this study if they were aged 65 years or older and were screened as either prefrail (scores of 1‐2 on the FRAIL [Fatigue, Resistance, Ambulation, Illness, and Loss of weight] scale) or frail (scores of 3‐5 on the FRAIL scale) [Morley JE, Malmstrom TK, Miller DK. A simple frailty questionnaire (FRAIL) predicts outcomes in middle aged African Americans. J Nutr Health Aging. Jul 2012;16(7):601-608. [CrossRef] [Medline]2]. To ensure the safety of the participants, older adults were excluded from participating if they reported having specific conditions. Specific exclusion criteria are described in

Multimedia Appendix 2

Additional information about study methods and attendance.

The sample size was calculated based on an estimated 0.5-point improvement in the FRAIL score (SD 1) between an exercise condition versus lifestyle education, using a 2-sided test at 1% significance level with 80% power. Assuming a 20% dropout rate, the minimum sample size is 120 per arm. It was estimated that about 1 in 10 older adults was frail. To allow subgroup analysis by frailty status, the ratio of participants with prefrailty to those with frailty was set at about 6:4 (

Multimedia Appendix 2

Additional information about study methods and attendance.

Randomization and Masking

As shown in

Multimedia Appendix 3

Components and sequence of the 3-arm trial.

Randomization (1:1:1) was done by a research assistant using computer-generated random numbers stratified by frailty status. The person who was responsible for generating the random allocation sequence was not involved in any other parts of the research. Each group of consecutive participants was assigned to one of the 3 arms. Group allocation could not be masked for persons delivering or receiving the interventions. Our program exercise physiologists, who were responsible for developing the exercise protocols, training exercise coaches, and conducting the fitness tests with participants, were blind to the group assignment. Research assistants designated to assess outcomes were blind to group assignment and had no involvement in the delivery of interventions.

Intervention Program: GrandMove

The GrandMove program is a structured exercise training program that contains 2 protocols, one focusing on aerobic exercise and the other on resistance exercise. Two protocols for aerobic training and resistance training were designed by our program exercise physiologists with certified training in strength and conditioning and tailored for older adults with prefrailty and frailty in Hong Kong. Robust older people were trained as exercise coaches to deliver the exercise protocols. The design of the program was guided by social learning theory [Bandura A. Social Learning Theory. Prentice-Hall; 1977. ISBN: 013816751612] and behavioral principles [Lally P, Gardner B. Promoting habit formation. Health Psychol Rev. May 2013;7(sup1):S137-S158. [CrossRef]13] (see

Multimedia Appendix 1

Program design.

The lifestyle education condition was comprised of 12 group sessions of health talks and 36 telehealth sessions. All health talks that covered different topics were delivered in a small group format by a retired nurse. Telehealth sessions involved a research assistant reviewing the health topics with participants and consolidating their understanding over the phone.

Each exercise intervention component lasted for 6 months (

Multimedia Appendix 4

Schedule for each intervention component.

Measures

The participants were assessed at baseline, 6 months, 12 months, and 18 months. Each assessment included a battery of self-report instruments administered through a structured interview and physical tests. Basic demographic characteristics were obtained, including age, gender, education level, marital status, and living arrangement.

Primary Outcomes

There were 3 primary outcomes. First, the frailty score was calculated using the 5-item FRAIL scale [Morley JE, Malmstrom TK, Miller DK. A simple frailty questionnaire (FRAIL) predicts outcomes in middle aged African Americans. J Nutr Health Aging. Jul 2012;16(7):601-608. [CrossRef] [Medline]2]. The items cover areas of fatigue, resistance, aerobic fitness, illnesses, and loss of weight. FRAIL scores are classified into three categories: robust (score of 0), prefrail (score of 1-2), and frail (score of 3-5). Second, physical performance was measured using the Short Physical Performance Battery (SPPB) [Guralnik JM, Simonsick EM, Ferrucci L, et al. A short physical performance battery assessing lower extremity function: association with self-reported disability and prediction of mortality and nursing home admission. J Gerontol. Mar 1994;49(2):M85-M94. [CrossRef] [Medline]14]. The SPPB score ranges from 0‐12, with a higher score indicating better performance. Third, quality of life was measured using the World Health Organization Quality of Life – Older adults module (WHOQoL-OLD) scale validated in a Chinese population [Liu R, Wu S, Hao Y, et al. The Chinese version of the World Health Organization Quality of Life instrument-older adults module (WHOQOL-OLD): psychometric evaluation. Health Qual Life Outcomes. Sep 16, 2013;11(156):24034698. [CrossRef] [Medline]15]. The total score ranges from 0‐100, with a higher score indicating better quality of life.

Secondary Outcomes

There were 3 fitness performance measures including isometric handgrip strength as measured by a digital hand dynamometer (Jamar Plus+), the 30-second arm curl test [James TW. The 30-second arm curl test as an indicator of upper body strength in older adults [Dissertation]. California State University; 1999. URL: https:/​/www.​proquest.com/​dissertations-theses/​30-second-arm-curl-test-as-indicator-upper-body/​docview/​304580972/​se-2 [Accessed 2025-04-30] 16], and the 2-minute step test [Rikli RE, Jones CJ. Functional fitness normative scores for community-residing older adults, ages 60-94. J Aging Phys Act. 1999;7(2):162-181. [CrossRef]17]. The hand grip strength of each hand was the average score of 3 trials. Higher fitness scores indicate better performance.

Other secondary outcomes included instrumental activities of daily living (IADL) as measured using the Lawton IADL scale (score range 0‐100, with higher scores indicating a lower level of disability) [Lawton MP, Brody EM. Assessment of older people: self-maintaining and instrumental activities of daily living. Gerontologist. 1969;9(3):179-186. [Medline]18], level of physical activity as measured using the Physical Activity Scale for the Elderly (PASE; higher scores indicate a higher level of physical activity) [Washburn RA, McAuley E, Katula J, Mihalko SL, Boileau RA. The physical activity scale for the elderly (PASE): evidence for validity. J Clin Epidemiol. Jul 1999;52(7):643-651. [CrossRef] [Medline]19], sleep quality as measured using the Pittsburgh Sleep Quality Index (PSQI; higher scores indicate worse overall sleep quality) [Buysse DJ, Reynolds CF 3rd, Monk TH, Hoch CC, Yeager AL, Kupfer DJ. Quantification of subjective sleep quality in healthy elderly men and women using the Pittsburgh Sleep Quality Index (PSQI). Sleep. Aug 1991;14(4):331-338. [CrossRef] [Medline]20], social functioning as measured using the Lubben Social Network Scale (LSNS; higher scores indicate a greater level of social support) [Lubben J, Blozik E, Gillmann G, et al. Performance of an abbreviated version of the Lubben Social Network Scale among three European community-dwelling older adult populations. Gerontologist. Aug 2006;46(4):503-513. [CrossRef] [Medline]21], and depressive symptoms as measured using the Patient Health Questionnaire-9 (PHQ-9; score range 0‐27, with higher scores indicating greater symptom severity) [Kroenke K, Spitzer RL, Williams JB. The PHQ-9: validity of a brief depression severity measure. J Gen Intern Med. Sep 2001;16(9):606-613. [CrossRef] [Medline]22].

Statistical Analysis

We conducted all analyses on an intention-to-treat basis. We generated descriptive statistics for baseline characteristics. The proportions of participants who achieved a robust or an improved frailty status (from frail to prefrail/robust or from prefrail to robust) at each follow-up were described. Within-group changes in proportions of robust or improved frailty outcome were tested using mixed effect logistic regression models.

The difference in outcome measures between intervention groups was estimated at each follow-up time point using repeated measures mixed effect linear regression models, adjusting for the fixed effects of gender and age at baseline. The main analysis using mixed models in the whole sample will further adjust for other baseline covariates that were found to be significantly different between groups. To examine the effectiveness of 6-month aerobic or resistance training, outcomes in the A-R-E group and R-A-E group were compared to the E-R-A group. To investigate the order effect in aerobic and resistance training, we compared 12-month outcomes between the R-A-E group and the A-R-E group (reference group). To evaluate the maintenance of exercise effect and habit formation, we compared the outcomes including the level of physical activity between groups at 18 months. As intervention components were switched at the 6th and 12th month, time was treated as a categorical variable instead of continuous to account for the possible nonlinear relationship between time and outcome variables. Treatment effect referred to the coefficient of the intervention group × time interaction. Subgroup analyses by baseline frailty status and gender were individually made to delineate the differential treatment effects. Since 12 outcomes were examined in this study, we set the significance level at 1% and reported the 99% CIs for the primary outcomes to account for multiple comparison bias. The significance level for the secondary outcomes was set at 5%. All analyses were conducted using Stata/MP (version 17.0; StataCorp LLC).

Results

Sample Characteristics

In total, 723 potential participants were assessed for eligibility, of whom 390 (53.9%) were randomized (Figure 1). Of the 390 participants included in the study, 132 (33.8%) were assigned to the E-R-A group, 124 (31.8%) to A-R-E, and 134 (34.4%) to R-A-E.

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Baseline characteristics for participants by intervention group are shown in Table 1. The average FRAIL score, SPPB score, and overall quality of life at baseline were 2.1 (SD 0.9), 7.8 (SD 2.8), and 91.6 (SD 13.1), respectively. Characteristics of participants in the 3 groups were similar, except for the quality of life (F_2,385=3.26, P=.04) and arm curl test scores (F_2,382=5.47, P=.005). As suggested by the mean PASE scores, all 3 groups were considered as having low activity levels in general [Laddu D, Parimi N, Cauley JA, et al. The association between trajectories of physical activity and all-cause and cause-specific mortality. J Gerontol A Biol Sci Med Sci. Nov 10, 2018;73(12):1708-1713. [CrossRef] [Medline]23]. No reports of adverse events that led to death, hospitalization, or medical attendance were received by the end of the program.

	Ea-Rb-Ac group (n=132)	A-R-E group (n=124)	R-A-E group (n=134)	F/χ2 (df)	P value
Age (years), mean (SD)	80.5 (7.5)	80.9 (7.1)	81.2 (7.4)	F=0.25 (2, 387)	.78
Gender, female, n (%)	106 (80.3)	97 (78.2)	105 (78.4)	χ2=0.21 (2)	.90
Education, n (%)				χ2=6.15 (6)	.41
No formal education	79 (59.9)	66 (53.2)	73 (54.5)
Primary school	27 (20.5)	29 (23.4)	30 (22.4)
Junior middle school	11 (8.3)	10 (8.1)	19 (14.2)
High school or above	15 (11.4)	19 (15.3)	12 (9)
Marital status, n (%)				χ2=2.04 (4)	.73
Married	47 (35.6)	49 (40.2)	45 (33.8)
Widowed	75 (56.8)	62 (50.8)	79 (59.4)
Others	10 (7.6)	11 (9)	9 (6.8)
Living alone	38 (28.8)	46 (37.4)	47 (35.3)	χ2=2.34 (2)	.31
Frailty status, n (%)				χ2=0.70 (2)	.70
Prefrail	80 (60.6)	80 (64.5)	80 (59.7)
Frail	52 (39.4)	44 (35.5)	54 (40.3)
5-item FRAILd scale, mean (SD)	2.2 (0.9)	2.1 (0.9)	2.1 (1)	F=0.27 (2, 387)	.76
SPPBe, mean (SD)	8 (2.7)	7.5 (2.9)	7.8 (2.9)	F=1.14 (2, 387)	.32
WHOQoL-OLDf, mean (SD)	93.5 (12.3)	91.9 (12.4)	89.4 (14.1)	F=3.26 (2, 385)	.04
Grip strength (left hand), mean (SD)	34.5 (11.5)	33.6 (12.7)	33 (14.6)	F=0.46 (2, 381)	.63
Grip strength (right hand), mean (SD)	36.2 (12.6)	33.7 (13)	35.7 (14.9)	F=0.06 (2, 382)	.94
30-s arm curl test, mean (SD)	12.1 (4.3)	10.6 (4.3)	10.5 (4.1)	F=5.47 (2, 382)	.005
2-min step test, mean (SD)	69.2 (28.2)	65.3 (28.2)	66.6 (30.8)	F=0.60 (2, 382)	.55
IADLg, mean (SD)	14.8 (2.7)	15.2 (3.1)	15.2 (2.7)	F=0.99 (2, 385)	.37
PASEh, mean (SD)	70.6 (41.9)	73.1 (41.7)	72.3 (47.7)	F=0.11 (2, 382)	.90
LSNSi, mean (SD)	21.1 (9.6)	21.8 (9.5)	21.4 (9.7)	F=0.14 (2, 385)	.87
PSQIj, mean (SD)	8.3 (4.3)	8.1 (3.9)	8.3 (3.7)	F=0.10 (2, 356)	.91
PHQ-9k, mean (SD)	4 (4.9)	3.8 (4.7)	3.3 (4.5)	F=0.86 (2, 384)	.42

^aE: lifestyle education.

^bR: resistance training.

^cA: aerobic training.

^dFRAIL: Fatigue, Resistance, Ambulation, Illness, and Loss of weight.

^eSPPB: Short Physical Performance Battery.

^fWHOQoL-OLD: Cantonese version of the World Health Organization Quality of Life – Older adults module.

^gIADL: Lawton’s Instrumental Activities of Daily Living scale.

^hPASE: Physical Activity Scale for the Elderly.

ⁱLSNS: Lubben Social Network Scale.

^jPSQI: Pittsburgh Sleep Quality Index.

^kPHQ-9: Patient Health Questionnaire-9.

Change in Frailty Status

We found a substantial overall improvement in frailty status (Figure 2 and Multimedia Appendices 5 and Travers J, Romero-Ortuno R, Bailey J, Cooney MT. Delaying and reversing frailty: a systematic review of primary care interventions. Br J Gen Pract. Jan 2019;69(678):e61-e69. [CrossRef] [Medline]6), both in terms of achieving a robust status and an improved status (from frail to prefrail/robust or from prefrail to robust).

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In the prefrail sample, 35.8% (76/212) of all participants became robust after 6 months. The proportion of robust participants increased to 51.0% (98/192) at 12 months and remained stable (83/164, 50.6%) at 18 months. In the frail sample, 17.9% (24/134) of participants became robust at 6 months. The proportion increased to 20.4% (23/113) at 12 months and continually increased to 25% (25/100) at 18 months. In terms of within-group changes, participants from the E-R-A group and A-R-E group (prefrail sample only) continued to have a significant improvement in frailty beyond 6 months (Figure 2 and Multimedia Appendices 5 and Travers J, Romero-Ortuno R, Bailey J, Cooney MT. Delaying and reversing frailty: a systematic review of primary care interventions. Br J Gen Pract. Jan 2019;69(678):e61-e69. [CrossRef] [Medline]6). Although a smaller proportion of participants with frailty obtained a robust status within the first 6 months, the majority of them progressed to prefrailty.

Aerobic Versus Resistance Training: 6-Month Outcomes

As shown in Table 2, there was an overall improvement (having a significant time effect) in FRAIL score (coefficient −0.81, 95% CI −1.09 to –0.52; P<.001), IADL (coefficient 0.48, 95% CI 0.04 to 0.91; P=.03), PSQI (coefficient −0.74, 95% CI −1.34 to –0.14; P=.02), and PHQ-9 (coefficient −0.98, 95% CI −1.81 to −0.16; P=.02) in all groups over 6 months, suggesting that participants had improved frailty and functional and psychological outcomes.

	Baseline to 6 months		Baseline to 12 months		Baseline to 18 months
	Coefficient (95% or 99% CI)	P value	Coefficient (95% or 99% CI)	P value	Coefficient (95% or 99% CI)	P value
5-item FRAILascale
Time effect	−0.81 (−1.09 to −0.52)	<.001	−1.10 (−1.40 to −0.80)	<.001	−1.06 (−1.36 to −0.75)	<.001
A-R-Eb group × time	0.07 (−0.35 to 0.49)	.68	0.16 (−0.27 to 0.60)	.33	0.16 (−0.29 to 0.62)	.35
R-A-E group × time	−0.02 (−0.42 to 0.38)	.90	0.25 (−0.17 to 0.67)	.13	0.20 (−0.23 to 0.64)	.23
SPPBc
Time effect	−0.22 (−0.66 to 0.31)	.20	−0.61 (−1.08 to −0.15)	.003	−0.64 (−1.11 to −0.16)	.002
A-R-E group × time	0.15 (−0.51 to 0.80)	.57	0.27 (−0.41 to 0.95)	.31	0.34 (−0.25 to 1.34)	.22
R-A-E group × time	0.03 (−0.60 to 0.65)	.91	0.04 (−0.62 to 0.70)	.88	−0.22 (−0.90 to 0.46)	.52
WHOQoL-OLDd
Time effect	0.22 (−2.62 to 3.07)	.84	1.66 (−1.31 to 4.63)	.15	0.52 (−2.53 to 3.57)	.66
A-R-E group × time	3.34 (−0.85 to 7.52)	.04	−0.73 (−5.10 to 3.63)	.66	1.85 (−2.75 to 6.45)	.30
R-A-E group × time	5.23 (1.21 to 9.24)	.001	3.77 (−0.47 to 8.01)	.02	4.13 (−0.23 to 8.49)	.02
Grip strength (left)
Time effect	−2.81 (−4.31 to −1.30)	<.001	−0.22 (−1.81 to 1.36)	.78	Not reported
A-R-E group × time	2.99 (0.76 to 5.23)	.009	0.20 (−2.14 to 2.54)	.87
R-A-E group × time	2.21 (0.63 to 4.36)	.04	−0.55 (−2.82 to 1.72)	.63
Grip strength (right)
Time effect	−3.12 (−4.62, to –1.63)	<.001	−1.12 (−1.12 to 0.45)	.16	Not reported
A-R-E group × time	3.75 (1.54 to 5.97)	.001	1.06 (−1.25 to 3.38)	.37
R-A-E group × time	2.29 (0.16 to 4.42)	.04	−0.50 (−2.75 to 1.75)	.66
30-s arm curl
Time effect	−0.77 (−0.78 to 0.63)	.83	0.12 (−0.62 to 0.85)	.76	0.12 (−0.63 to 0.88)	.75
A-R-E group × time	1.42 (0.39 to 2.46)	.007	1.46 (0.38 to 2.54)	.008	0.52 (−0.63 to 1.66)	.38
R-A-E group × time	1.11 (0.12 to 2.11)	.03	1.03 (−0.02 to 2.09)	.054	0.65 (−0.44 to 1.73)	.24
2-min step test
Time effect	2.75 (−1.81 to 7.31)	.24	8.46 (3.69 to 13.24)	.001	7.99 (2.99 to 12.85)	.002
A-R-E group × time	5.51 (−1.23 to 12.25)	.11	2.49 (−4.57 to 9.54)	.49	1.10 (−6.32 to 8.52)	.77
R-A-E group × time	1.38 (−5.09 to 7.84)	.68	−3.17 (−9.99 to 3.66)	.36	−4.46 (−11.50 to 2.59)	.22
IADLe
Time effect	0.48 (0.04 to 0.91)	.03	0.64 (0.19 to 1.09)	.006	0.74 (0.27 to 1.20)	.002
A-R-E group × time	−0.32 (−0.95 to 0.32)	.33	-0.77 (−1.43 to −0.11)	.02	-0.88 (−1.59 to −0.18)	.01
R-A-E group × time	−0.38 (−0.99 to 0.24)	.23	−1.09 (−1.74 to 0.45)	.001	−1.22 (−1.89 to −0.56)	<.001
PASEh
Time effect	2.25 (−6.18 to 10.67)	.60	3.11 (−5.67 to 11.89)	.49	10.99 (2.06 to 19.90)	.02
A-R-E group × time	4.65 (−7.70 to 17.00)	.46	0.37 (−12.45 to 13.19)	.96	−3.29 (−16.72 to 10.14)	.63
R-A-E group × time	2.32 (−9.59 to 14.24)	.70	0.88 (−11.60 to 13.36)	.89	−3.00 (−15.76 to 9.77)	.64
LSNSf
Time effect	0.89 (−0.66 to 2.44)	.26	2.43 (0.81 to 4.06)	.003	1.39 (−0.27 to 3.06)	.10
A-R-E group × time	−1.73 (−4.02 to 055)	.14	−1.82 (−4.21 to 0.56)	.13	−0.68 (−3.20 to 1.83)	.60
R-A-E group × time	−0.48 (−2.67 to 1.72)	.67	−1.28 (−3.60 to 1.04)	.28	0.23 (−2.15 to 2.62)	.85
PSQIg
Time effect	−0.74 (−1.34 to −0.14)	.02	−0.96 (−1.59 to −0.33)	.003	0.17 (−0.48 to 0.81)	.61
A-R-E group × time	0.47 (−0.43 to 1.36)	.31	1.16 (0.23 to 2.09)	.02	−0.31 (−1.29 to 0.68)	.54
R-A-E group × time	0.58 (−0.28 to 1.44)	.19	0.94 (0.03 to 1.85)	.04	0.64 (−0.29 to 1.57)	.18
PHQ-9i
Time effect	−0.98 (−1.81 to −0.16)	.02	−1.14 (−2.00 to −0.27)	.01	−1.19 (−2.38 to −0.61)	.001
A-R-E group × time	0.43 (−0.79 to 1.65)	.49	0.49 (−0.78 to 1.76)	.45	0.69 (−0.65 to 2.03)	.31
R-A-E group × time	1.34 (0.17 to 2.52)	.02	1.51 (0.27 to 2.75)	.02	2.14 (0.87 to 3.41)	.001

^aFRAIL: Fatigue, Resistance, Ambulation, Illness, and Loss of weight.

^bA: aerobic training, R: resistance training, E: lifestyle education.

^cSPPB: Short Physical Performance Battery.

^dWHOQoL-OLD: Cantonese version of the World Health Organization Quality of Life - Older adults module.

^eIADL: Lawton’s Instrumental Activities of Daily Living scale.

^fLSNS: Lubben Social Network Scale.

^gPASE: Physical Activity Scale for the Elderly.

^hPSQI: Pittsburgh Sleep Quality Index.

ⁱPHQ-9: Patient Health Questionnaire-9.

^jMeasurements reporting 99% CI: 5-item FRAIL scale, SPPB, and WHOQoL-OLD. All other scales used 95% CI.

At 6 months, participants with resistance training (R-A-E group) compared with those with lifestyle education (E-R-A group) had greater improvement in quality of life (interaction coefficient 5.23, 99% CI 1.21 to 9.24; P<.001) but not in FRAIL score and SPPB. Similar findings were observed in the prefrail subsample (

Multimedia Appendix 7

Summary of time and group × time interaction effects on primary and secondary outcomes (participants with prefrailty only).

For the secondary outcomes, both aerobic training (A-R-E group) and resistance training (R-A-E group) performed better in several fitness outcomes than the E-R-A group. The A-R-E group was associated with greater improvement in left hand grip strength (interaction coefficient 2.99, 95% CI 0.76 to 5.23; P=.009), right hand grip strength (interaction coefficient 3.75, 95% CI 1.54 to 5.97; P=.001), and the arm curl test (interaction coefficient 1.42, 95% CI 0.39 to 2.46; P=.007) than lifestyle education (E-R-A group). The R-A-E group was also associated with greater improvement in the 3 outcomes (Table 2). The A-R-E and R-A-E groups did not differ from the E-R-A group in all other nonfitness measures including the 2-minute step test, IADL, PASE, LSNS, and PSQI over 6 months. The R-A-E group had a significantly higher level of PHQ-9 scores (interaction coefficient 1.34, 95% CI 0.17 to 2.52; P=.02). Results of the subgroup analysis by frailty status were summarized in Multimedia Appendices 7 and Izquierdo M, Merchant RA, Morley JE, et al. International exercise recommendations in older adults (ICFSR): expert consensus guidelines. J Nutr Health Aging. 2021;25(7):824-853. [CrossRef] [Medline]8, whereas results of the subgroup analysis by gender were summarized in Multimedia Appendices 9 and Tseng BS, Marsh DR, Hamilton MT, Booth FW. Strength and aerobic training attenuate muscle wasting and improve resistance to the development of disability with aging. J Gerontol A Biol Sci Med Sci. Nov 1995;50 Spec No:113-119. [CrossRef] [Medline]10.

Aerobic and Resistance Training: The Order Effect (12-Month Outcomes)

To compare the order effect, we also compared the R-A-E group with the A-R-E group (reference group) on 12-month outcomes (

Multimedia Appendix 11

Comparison of outcomes between the R-A-E group and A-R-E group (reference) at the 12-month follow-up.

In sum, the findings suggested that the order of aerobic and resistance training did not have an impact on fitness outcome at 12 months, although some preliminary data suggested that undergoing resistance training before aerobic training might improve quality of life.

Maintenance of Exercise Effect and Habit Formation

The A-R-E and R-A-E groups did not receive a physical intervention between 12 and 18 months. If exercise effects were maintained, we expected to observe gains to be maintained by the end of the study. As shown in Table 2, the improvement in WHOQoL-OLD seemed to be maintained at 18 months in these 2 groups compared to the E-R-A group but the P value did not reach the .01 threshold (interaction coefficient 4.13, 95% CI −0.23 to 8.49; P=.02).

However, the gains in IADL appeared to reduce in the A-R-E (interaction coefficient −0.88, 95% CI −1.59 to −0.18; P=.013) and the R-A-E groups (interaction coefficient −1.22, 95% CI −1.89 to −0.56; P<.001) and also for PHQ-9 in the R-A-E group (interaction coefficient 2.14, 95% CI 0.87 to 3.41; P=.001).

Neither aerobic training nor resistance training improved PASE at 6 months compared to lifestyle education. We observed a significant time effect on PASE over 18 months in the whole sample (coefficient 10.99, 95% CI 2.06 to 19.90; P=.02) and in the frail subsample (coefficient 14.6, 95% CI 1.39 to 27.81; P=.03), indicating that combined exercise and lifestyle education, regardless of intervention sequence, might improve individuals’ level of physical activity.

Discussion

Principal Findings

This study examined the effectiveness of both aerobic training and resistance training using a sequential cluster randomized controlled trial design, which enabled us to examine how these physical activity interventions and their sequence might influence frailty outcomes. Although lifestyle education was initially added as a comparator intervention, our findings have demonstrated that the 18-month intervention combining lifestyle education and physical interventions is a viable strategy to address frailty and is health-promoting. The frailty score improved across groups, providing further evidence that physical frailty is reversible. Our study also produced a few other key findings. Aerobic training or resistance training tended to improve fitness performance but was not superior to an intensive lifestyle education program in addressing frailty. It is possible that 6 months of resistance training followed by another 6 months of aerobic training might be better at improving quality of life. Although the overall improvement in frailty outcome was maintained over 18 months, IADL and PHQ-9 appeared to worsen over the post–physical intervention period. We observed a small increase in the level of physical activity over 18 months, but its relation to the formation of exercise habits and an active lifestyle is yet to be determined.

Despite physical activity intervention being the most widely studied and recommended approach for the management of frailty [Fit for frailty: consensus best practice guidance for the care of older people living with frailty in community and outpatient settings. British Geriatrics Society; 2014. URL: https://www.bgs.org.uk/sites/default/files/content/resources/files/2018-05-14/fff2_short_0.pdf [Accessed 2025-04-30] 24], we found that a single-mode exercise program (aerobic or resistance) for 6 months was no better than lifestyle education in addressing frailty. The findings coincided with a recent systematic review suggesting that physical activity intervention, when compared with an active control intervention, was not associated with a significant reduction in frailty [Negm AM, Kennedy CC, Thabane L, et al. Management of frailty: a systematic review and network meta-analysis of randomized controlled trials. J Am Med Dir Assoc. Oct 2019;20(10):1190-1198. [CrossRef] [Medline]25]. We found that the administration of 2 physical interventions in sequence did not further improve frailty scores but participants were able to maintain the gain accrued over the first 6 months. The 3 study arms approximated a multifaceted intervention that incorporated physical, psychosocial, and educational components. There were a few multifaceted studies [Oh SL, Kim HJ, Woo S, et al. Effects of an integrated health education and elastic band resistance training program on physical function and muscle strength in community-dwelling elderly women: Healthy Aging and Happy Aging II study. Geriatr Gerontol Int. May 2017;17(5):825-833. [CrossRef] [Medline]26-Spoorenberg SLW, Wynia K, Uittenbroek RJ, Kremer HPH, Reijneveld SA. Effects of a population-based, person-centred and integrated care service on health, wellbeing and self-management of community-living older adults: a randomised controlled trial on Embrace. PLoS One. 2018;13(1):e0190751. [CrossRef] [Medline]28] but cross-study comparison was difficult due to their different designs and the lack of frailty as an outcome. The Hatoyama Cohort Study [Seino S, Nishi M, Murayama H, et al. Effects of a multifactorial intervention comprising resistance exercise, nutritional and psychosocial programs on frailty and functional health in community-dwelling older adults: a randomized, controlled, cross-over trial. Geriatr Gerontol Int. Nov 2017;17(11):2034-2045. [CrossRef] [Medline]27] found that resistance exercise in combination with nutritional education and psychosocial programs for 3 months successfully reduced the prevalence of frailty by 24%. Our study further added that the sequence of intervention components, if not delivered concurrently, might not make a significant difference. Nonetheless, older adults with frailty may find the program more acceptable if they have greater control over the sequence of interventions.

We added to the literature that psychosocial intervention might be complementary to physical activity intervention for the management of frailty. Following the lifestyle education program, the subsequent addition of physical intervention appeared to generate further gain. Participants from the E-R-A group were observed to have continued improvement in frailty outcomes after switching from lifestyle education to resistance training. There were only a few known studies to date exploring the effectiveness of psychosocial interventions on frailty. A Swedish study evaluated a 4-week senior group program similar to our lifestyle education program, which introduced and discussed various healthy lifestyle topics [Gustafsson S, Wilhelmson K, Eklund K, et al. Health-promoting interventions for persons aged 80 and older are successful in the short term--results from the randomized and three-armed Elderly Persons in the Risk Zone study. J Am Geriatr Soc. Mar 2012;60(3):447-454. [CrossRef] [Medline]29]. The senior group program had no impact on frailty outcomes, but it was reported to delay activities of daily living deterioration. Our lifestyle education program was more intensive in terms of frequency and duration than the senior group program. Further studies may explore whether shorter or longer combined interventions may make a difference in frailty outcomes.

Since frailty is suggested to result from cumulative declines in multiple physiologic systems [Fried LP, Tangen CM, Walston J, et al. Frailty in older adults: evidence for a phenotype. J Gerontol A Biol Sci Med Sci. Mar 2001;56(3):M146-M156. [CrossRef] [Medline]1], it is not surprising that interventions targeting different systems may yield similar positive results (ie, the equifinality principle). There might be common factors across the intervention approaches that mitigate frailty, such as social support from peers (exercise coaches and retired nurses). In our study, all 3 intervention components encouraged social engagement through the group sessions and peer coaching. Previous studies have suggested that social support might directly or indirectly contribute to higher levels of physical activity in older adults [Lieber SB, Moxley J, Mandl LA, Reid MC, Czaja SJ. Social support and physical activity: does general health matter? Eur Rev Aging Phys Act. Jun 20, 2024;21(1):16. [CrossRef] [Medline]30-Smith GSE, Moyle W, Burton NW. The relationship between social support for physical activity and physical activity across nine years in adults aged 60-65 years at baseline. Int J Environ Res Public Health. Mar 3, 2023;20(5):36901538. [CrossRef] [Medline]32] and could therefore be health-promoting and lead to a healthier lifestyle. Further studies should include a comparison group without social influence and a measure of perceived social support to allow for an estimation of its impact on frailty and quality of life. Future studies may also include measures of other psychological mediators such as self-efficacy, enjoyment, and the use of behavioral and cognitive processes [Lewis BA, Marcus BH, Pate RR, Dunn AL. Psychosocial mediators of physical activity behavior among adults and children. Am J Prev Med. Aug 2002;23(2 Suppl):26-35. [CrossRef] [Medline]33] for mediation analyses.

The subgroup analysis by frailty status showed that participants with frailty appeared to have a greater magnitude of reduction in FRAIL score, further demonstrating that frailty is a modifiable condition. The frail subgroup also had consistently reported increased social engagement and some reduction in depressive symptoms over 18 months. Some improvements in physical fitness were observed but may not have been sustained beyond the active intervention period. The results echoed our hypothesis that active physical or psychosocial interventions might enhance social support for older adults at high risk of vulnerability and social isolation [Lindsay Smith G, Banting L, Eime R, O’Sullivan G, van Uffelen JGZ. The association between social support and physical activity in older adults: a systematic review. Int J Behav Nutr Phys Act. Apr 27, 2017;14(1):56. [CrossRef] [Medline]34]. Physical activity guidelines should recommend older adults with frailty to engage in moderate-intensity exercise regularly [Izquierdo M, Duque G, Morley JE. Physical activity guidelines for older people: knowledge gaps and future directions. Lancet Healthy Longev. Jun 2021;2(6):e380-e383. [CrossRef] [Medline]35]. The design of physical activity interventions should incorporate social or group elements that enhance social learning and reinforcement. With a sample predominantly comprised of female older adults (~80%), the results for the female subsample were largely consistent with those in the full sample. There may be a lack of power to detect significant intervention effects in the male subsample. These results should be interpreted with caution.

We observed a significant increase in the level of physical activity over 18 months, probably due in part to the significant change within the frail subsample. No evidence showed that participants with prefrailty increased their level of physical activity after interventions. It might take as long as 18 months to observe an overall increase in the level of physical activity. The potential of exercise and lifestyle interventions to modify long-term exercise habits remains unclear. It is common to observe a relapse pattern in health behavior once an intervention has ended [Wood W, Neal DT. Healthy through habit: interventions for initiating & maintaining health behavior change. Behavioral Science & Policy. Apr 2016;2(1):71-83. [CrossRef]36]. Program effectiveness and acceptability are equally important as pain and discomfort associated with physical activity could be an obstacle to engaging in further physical activity [Wang Z, Fang Y, Chan PSF, Yu FY, Sun F. The changes in levels and barriers of physical activity among community-dwelling older adults during and after the fifth wave of COVID-19 outbreak in Hong Kong: repeated random telephone surveys. JMIR Aging. Jan 23, 2023;6:e42223. [CrossRef] [Medline]37]. In addition, a physical intervention combined with smartphone-assisted e-reminders, an activity tracker, and e-coaching may help habit formation [Kwan RY, Lee D, Lee PH, et al. Effects of an mHealth brisk walking intervention on increasing physical activity in older people with cognitive frailty: pilot randomized controlled trial. JMIR mHealth uHealth. Jul 31, 2020;8(7):e16596. [CrossRef] [Medline]38]. It is equally important to implement strategies to discourage unhealthy habits simultaneously. It is possible that our lifestyle education program helped increase participants’ awareness about unhealthy habits and alternative healthy options in the environment. Further investigation to determine the optimal form of intervention(s) that best maintains exercise habit formation is warranted.

We consider the delivery of exercise interventions by peer coaches to be the key to long-term scalability and sustainability in the context of population aging. More research is needed to formally evaluate the sustainability and cost-effectiveness of the intervention model. Future research should consider the productive aging component for engaging retired older adults in productive activities, task shifting from health professionals to more available human resources (ie, peer coaches), and the implications of an increased number of robust older people in the community. Health care utilization associated with a positive change in frailty outcomes has not been explored, but it is worth further investigation.

Limitations

Due to the complexity of the study design, we lacked a care-as-usual comparator group. The active control group only abstained from physical intervention in the first 6 months. Therefore, we were unable to evaluate the effectiveness of physical activity interventions for 12 months compared with an active control intervention. Further multifaceted intervention studies may include both psychoeducational components in combination with physical interventions. An accelerometer-based measure of physical activity level may be better than a self-reported one in estimating the effect of a physical intervention on habit formation [Valenti G, Bonomi AG, Westerterp KR. Walking as a contributor to physical activity in healthy older adults: 2 week longitudinal study using accelerometry and the doubly labeled water method. JMIR mHealth uHealth. Jun 7, 2016;4(2):e56. [CrossRef] [Medline]39]. Similar to other physical intervention programs, the generalization of results might be limited by attrition bias and a predominantly female sample. This program was tested in a densely populated community. This setting may enhance the viability and cost-effectiveness of delivering both group and home sessions via peer coaches. Adaptations may be needed if the model is applied in other contexts, for example, in rural areas, which will require a separate evaluation of feasibility and effectiveness.

Conclusions

In contrast to most previous trials, we attempted to address frailty by examining physical interventions in comparison with a novel comparator, that is, lifestyle education. Both tested physical interventions and lifestyle education were effective in improving frailty status. A simultaneous improvement in quality of life was observed. Participants with frailty appeared to benefit beyond a frailty outcome. Despite the positive findings, the impact of the interventions on exercise habit formation is yet to be investigated.