- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05397288
GrandMove Project to Promote Elders' Robustness Against Frailty (GrandMove)
Exercise Coaching Program With Aerobic Exercise and Resistance Exercise for Prefrail and Frail Older Adults
Study Overview
Status
Conditions
Detailed Description
This is a single-blind, cluster randomized, cross-over trial to investigate the effectiveness of (1) a 6-month aerobic exercise program led by trained young-old exercise coaches, (2) a 6-month resistance exercise program led by trained young-old exercise coaches, versus (3) a 6-month psychoeducation program on healthy lifestyle led by retired nurses for improving frailty, physical performance, and quality of life in frail/prefrail older persons. A total of 390 frail/prefrail older persons are randomized into one of the three programs in groups of 6 to 10 persons.
After 6 months, participants receive the other two programs in a pseudo random order to explore any effects of program sequence. The sequences are: (a) resistance exercise, aerobic exercise, psychoeducation; (b) aerobic exercise, resistance exercise, psychoeducation; and (c) psychoeducation, resistance exercise, aerobic exercise. The entire intervention period lasts for 18 months.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Non-US Or Canadian Address
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Hong Kong, Non-US Or Canadian Address, Hong Kong
- The University of Hong Kong
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- screened as frail or prefrail using cutoff scores of the 5-item FRAIL scale;
- living in the community and planned to reside in the area for the duration of the study;
- gave informed consent to participate in the study
Exclusion Criteria:
- heart failure, uncontrolled angina, severe pulmonary disease, or end-stage disease with a life expectancy of less than 18 months
- diagnosed dementia or a cutoff score falling below threshold suggestive of dementia using the clock-face test
- has another member of the household participating in the study
- difficulty in communication with study personnel due to speech or hearing problems
- other medical, psychiatric, or behavioural factors that may interfere with study participation or the ability to follow the intervention protocol
Temporary Exclusion Criteria:
- had stroke, hip fracture, myocardial infarction, major heart surgery, deep vein thrombosis, pulmonary embolus, spinal surgery, or hip or knee replacement within the previous 6 months;
- currently prescribed activity limitation or weight-bearing limitation by a formal healthcare professional;
- limited physical activity due to chest pain or dyspnoea without definitive treatment by a healthcare provider;
- currently consume more than 14 alcoholic drinks per week;
- currently enrolling in another randomized trial involving lifestyle or pharmacological interventions
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Resistance-Aerobic-Education (RAE)
Participants first receive 6 months of resistance exercise, then 6 months of aerobic exercise, and finally 6 months of education program on healthy lifestyle. Behavioral: Resistance exercise (R) Behavioral: Aerobic exercise (A) Behavioral: Healthy lifestyle education (E) |
A 6-month program led by trained young-old exercise coaches consisting of structured training with 5 progressive levels of intensity, with protocols for implementation in a home surrounding and community center settings. During the 6-month program, group practice and home visit (individual) sessions (45 mins each) are delivered in a tapering schedule:
A 6-month programs led by trained young-old exercise coaches consisting of structured training with 5 progressive levels of intensity, with protocols for implementation in a home surrounding and community center settings. During the 6-month program, group practice and home visit (individual) (45 mins each) are delivered in a tapering schedule:
A 6-month program led by retired nurses covering topics including nutrition, sleep, medication, cognition, and exercising. During the 6-month program, group talks and individual consultation (45 mins each) are delivered in a tapering schedule:
|
|
Experimental: Aerobic-Resistance-Education (ARE)
Participants first receive 6 months of aerobic exercise, then 6 months of resistance exercise, and finally 6 months of education program on healthy lifestyle. Behavioral: Aerobic exercise (A) Behavioral: Resistance exercise (R) Behavioral: Healthy lifestyle education (E) |
A 6-month program led by trained young-old exercise coaches consisting of structured training with 5 progressive levels of intensity, with protocols for implementation in a home surrounding and community center settings. During the 6-month program, group practice and home visit (individual) sessions (45 mins each) are delivered in a tapering schedule:
A 6-month programs led by trained young-old exercise coaches consisting of structured training with 5 progressive levels of intensity, with protocols for implementation in a home surrounding and community center settings. During the 6-month program, group practice and home visit (individual) (45 mins each) are delivered in a tapering schedule:
A 6-month program led by retired nurses covering topics including nutrition, sleep, medication, cognition, and exercising. During the 6-month program, group talks and individual consultation (45 mins each) are delivered in a tapering schedule:
|
|
Experimental: Education-Resistance-Aerobic (ERA)
Participants first receive 6 months of education program on healthy lifestyle, then 6 months of resistance exercise, and finally 6 months of aerobic exercise. Behavioral: Healthy lifestyle education (E) Behavioral: Resistance exercise (R) Behavioral: Aerobic exercise (A) |
A 6-month program led by trained young-old exercise coaches consisting of structured training with 5 progressive levels of intensity, with protocols for implementation in a home surrounding and community center settings. During the 6-month program, group practice and home visit (individual) sessions (45 mins each) are delivered in a tapering schedule:
A 6-month programs led by trained young-old exercise coaches consisting of structured training with 5 progressive levels of intensity, with protocols for implementation in a home surrounding and community center settings. During the 6-month program, group practice and home visit (individual) (45 mins each) are delivered in a tapering schedule:
A 6-month program led by retired nurses covering topics including nutrition, sleep, medication, cognition, and exercising. During the 6-month program, group talks and individual consultation (45 mins each) are delivered in a tapering schedule:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in physical frailty status measured by the 5-item FRAIL scale at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
|
Change in physical frailty status is measured by the 5-item FRAIL scale at baseline, 6 months, 12 months and 18 months.
It has a range of scores from 0 to 5, with 0 representing robust health status, 1-2 pre-frail, and 3-5 frail.
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in physical performance measured by Short Physical Performance Battery (SPPB) at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
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Change in physical performance measured by Short Physical Performance Battery (SPPB) at baseline, 6 months, 12 months and 18 months.
It has a range of scores from 0 to 12. Higher scores represent better physical performance, lower scores represent poor physical performance.
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in upper body strength measured by 30-second bicep curl test at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
|
Change in upper body strength measured by 30-second bicep curl test at baseline, 6 months, 12 months and 18 months.
Performance is defined by the frequency of arm curls completed in 30 seconds while sitting in a chair.
Higher frequencies represent better upper body strength, lower frequencies represent poor upper body strength.
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in aerobic exercise capacity measured by 2-minute step test at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
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Change in aerobic exercise capacity measured by 2-minute step test at baseline, 6 months, 12 months and 18 months.
Performance on the test is defined as the number of right-side steps of the criterion height completed in 2 minutes.
Higher frequencies represent better aerobic exercise capacity, lower frequencies represent poor aerobic exercise capacity.
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4 time points including: baseline, 6 months, 12 months, 18 months
|
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Change in quality of life measured by World Health Organization Quality of Life - Older Adult Module (WHOQoL-OLD) at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
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Change in quality of life measured by World Health Organization Quality of Life - Older Adult Module (WHOQoL-OLD) at baseline, 6 months, 12 months and 18 months.
It has a range of scores from 24 to 120.
Higher scores indicate better quality of life, lower scores indicate poor quality of life.
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in comprehensive frailty status measured by the 32-item Frailty Index (32-FI) at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
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Change in comprehensive frailty status measured by the 32-item Frailty Index (32-FI) at baseline, 6 months, 12 months and 18 months.
The index is calculated by the sum score divided by the total number of valid responses, ranging from 0 to 1. Frailty status is defined as: robust (FI ≤ 0.08), prefrail (0.08 < FI < 0.25), and frail (FI ≥ 0.25).
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4 time points including: baseline, 6 months, 12 months, 18 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in handgrip strength measured by the (Jamar® Hand Dynamometer - Plus+ Digital - 200 lb. Capacity) at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
|
Change in handgrip strength measured by the (Jamar® Hand Dynamometer - Plus+ Digital - 200 lb.
Capacity) at baseline, 6 months, 12 months and 18 months.
Performance is defined as the grip force exerted on the dynamometer.
Larger forces indicate better handgrip strength, smaller forces indicate poor handgrip strength.
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in pain severity measured by Face Pain Scale - Revised at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
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Change in pain severity measured by Face Pain Scale - Revised at baseline, 6 months, 12 months and 18 months.
It has a range of scores from 0 to 10, with 0 representing no pain, 10 representing very much pain.
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in physical activity measured by Physical Activity Scale for the Elderly (PASE) at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
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Change in physical activity measured by Physical Activity Scale for the Elderly (PASE) at baseline, 6 months, 12 months and 18 months.
It has a range of scores from 0 to 361, with higher scores indicating higher physical activity level and lower scores indicating lower physical activity level.
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in activities of daily living measured by Modified Barthel Index at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
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Change in activities of daily living measured by Modified Barthel Index at baseline, 6 months, 12 months and 18 months.
It has a range of scores from 0 to 100, with higher scores indicating independence and lower scores indicating dependence.
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in instrumental activities of daily living measured by Lawton Instrumental Activities of Daily Living at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
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Change in instrumental activities of daily living measured by Lawton Instrumental Activities of Daily Living at baseline, 6 months, 12 months and 18 months.
It has a range of scores from 0 to 18, with higher scores indicating independence and lower scores indicating dependence.
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in social network measured by Lubben Social Network Scale at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
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Change in social network measured by Lubben Social Network Scale at baseline, 6 months, 12 months and 18 months.
It has a range of scores from 0 to 50 (scores <20 are classified as isolated; 21-25 as high risk for isolation; 26-30 as moderate risk for isolation; ≥ 31 as low risk for isolation).
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in sleep quality measured by Pittsburgh Sleep Quality Index at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
|
Change in sleep quality measured by Pittsburgh Sleep Quality Index at baseline, 6 months, 12 months and 18 months.
It has a range of scores from 0 to 21, with higher scores indicating poor sleep quality and lower scores indicating better sleep quality.
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4 time points including: baseline, 6 months, 12 months, 18 months
|
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Change in nutrition status measured by Mini Nutritional Assessment-Short Form at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
|
Change in nutrition status measured by Mini Nutritional Assessment-Short Form at baseline, 6 months, 12 months and 18 months.
It has a range of scores from 0 to 30 (scores of 24-30 are classified as normal nutritional status; 17-23.5 as at risk of malnutrition; <17 as malnourished).
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in depressive symptoms measured by Patient Health Questionnaire - 9 (PHQ-9) at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
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Change in depressive symptoms measured by Patient Health Questionnaire - 9 (PHQ-9) at baseline, 6 months, 12 months and 18 months.
It has a range of scores from 0 to 27 (scores of 5-9 are classified as mild depression; 10-14 as moderate depression; 15-19 as moderately severe depression; ≥ 20 as severe depression)
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4 time points including: baseline, 6 months, 12 months, 18 months
|
|
Change in extent of mobility measured by the Life Space Questionnaire at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
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Change in extent of mobility measured by the Life Space Questionnaire at baseline, 6 months, 12 months and 18 months.
It has a range of scores from 0 to 9, reflecting the number of zones a person has moved in irrespective of the frequency and independence of these movements.
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in verbal fluency was measured by the Verbal Fluency Test at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
|
Change in verbal fluency was measured by the Verbal Fluency Test at baseline, 6 months, 12 months and 18 months.
Performance is defined by the number of items in a category that can be verbally listed in 60 seconds.
It has a range of scores from 0 to 20, with higher scores indicating higher verbal fluency and lower scores indicating lower verbal fluency.
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4 time points including: baseline, 6 months, 12 months, 18 months
|
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Change in cognitive performance measured by Digit Symbol Substitution Test at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
|
Change in cognitive performance measured by Digit Symbol Substitution Test at baseline, 6 months, 12 months and 18 months.
Performance is defined by the number of correct symbols substitution in 90 seconds.
It has a range of scores from 0 to 93, with higher scores indicating better cognitive performance and lower scores indicating poor cognitive performance.
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in logical memory was measured by the Logical Memory Test at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
|
Change in logical memory was measured by the Logical Memory Test at baseline, 6 months, 12 months and 18 months.
Performance is defined as the number of correct word items recalled.
It has a range of scores from 0 to 23, with higher scores indicating better logical memory and lower scores indicating poor logical memory.
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4 time points including: baseline, 6 months, 12 months, 18 months
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Change in digit span measured by the Digit Span Test at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
|
Change in digit span measured by the Digit Span Test at baseline, 6 months, 12 months and 18 months.
The sequence and span scores have a range from 0 to 8 for forward subsets, and the sequence and span scores have a range from 0 to 7 for backward subsets.
Higher scores indicating better cognitive performance and lower scores indicating poor cognitive performance.
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4 time points including: baseline, 6 months, 12 months, 18 months
|
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Change in health literacy measured by Chinese Health Literacy for Chronic Care at baseline, 6 months, 12 months and 18 months.
Time Frame: 4 time points including: baseline, 6 months, 12 months, 18 months
|
Change in health literacy measured by Chinese Health Literacy for Chronic Care at baseline, 6 months, 12 months and 18 months.
It has a range of scores from 0 to 48, and the cut-off score is 36 (≥ 36 indicates "adequate health literacy").
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4 time points including: baseline, 6 months, 12 months, 18 months
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in body composition measured by Dual-energy X-ray absorptiometry (DEXA) scanning at baseline and 6 months (outcome in frail subgroup only).
Time Frame: 2 time points including: baseline, 6 months
|
Change in body composition measured by Dual-energy X-ray absorptiometry (DEXA) scanning at baseline and 6 months (outcome in frail subgroup only).
The test results will be in the form T score (a score of -1 or above is classified as normal; a score between -1.1 and -2.4 is classified as osteopenia (low bone mass); a score of -2.5 and below is defined as osteoporosis).
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2 time points including: baseline, 6 months
|
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Change in functional muscular fitness measured by 30-second Chair Sit-to-stand Test at baseline and 6 months (outcome in frail subgroup only).
Time Frame: 2 time points including: baseline, 6 months
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Change in functional muscular fitness measured by 30-second Chair Sit-to-stand Test at baseline and 6 months (outcome in frail subgroup only).
The score is the number of stands a person can complete in 30 seconds, with higher scores indicating better functional muscular fitness and lower scores indicating poor functional muscular fitness.
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2 time points including: baseline, 6 months
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Change in upper and lower body strength measured by 3-repetition Maximum (3-RM) Test using Keiser pneumatic variable-resistance machines at baseline and 6 months (outcome in frail subgroup only).
Time Frame: 2 time points including: baseline, 6 months
|
Change in upper and lower body strength measured by 3-repetition Maximum (3-RM) Test using Keiser pneumatic variable-resistance machines at baseline and 6 months (outcome in frail subgroup only).
The score is defined as the maximum weight a person can lift for 3 repetitions.
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2 time points including: baseline, 6 months
|
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Change in cardiovascular fitness measured by Ergometers and MedGrapics Ultima CardiO2 Gas Exchange System at baseline and 6 months (outcome in frail subgroup only).
Time Frame: 2 time points including: baseline, 6 months
|
Change in cardiovascular fitness measured by Ergometers and MedGrapics Ultima CardiO2 Gas Exchange System at baseline and 6 months (outcome in frail subgroup only).
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2 time points including: baseline, 6 months
|
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Change in balance measured by Multifunctional force-measuring plate at baseline and 6 months (outcome in frail subgroup only).
Time Frame: 2 time points including: baseline, 6 months
|
Change in balance measured by Multifunctional force-measuring plate at baseline and 6 months (outcome in frail subgroup only).
|
2 time points including: baseline, 6 months
|
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Change in flexibility measured by Sit and Reach Flexibility Test at baseline and 6 months (outcome in frail subgroup only).
Time Frame: 2 time points including: baseline, 6 months
|
Change in flexibility measured by Sit and Reach Flexibility Test at baseline and 6 months (outcome in frail subgroup only).
The score is the recorded distance a person can reach forward by the hand with a seated position.
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2 time points including: baseline, 6 months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Terry YS Lum, PhD, HKU
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- EA1511048
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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