Promoting Health LongevIty Through Mitigation and Prevention of Frailty in Community-dwelling Elderly (Pro-LIFE)
NCT ID: NCT04656938
Last Updated: 2020-12-07
Study Results
Results pending
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
Recruitment Status
UNKNOWN
Clinical Phase
NA
Total Enrollment
700 participants
Study Classification
INTERVENTIONAL
Study Start Date
2018-05-01
Study Completion Date
2021-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The current healthcare response to frailty has been mainly reactive to acute health crises of the elderly. With its insidious onset and progression, frailty is often not apparent unless actively sought. Well-validated models of frailty already exist and, instead of trying to create new frailty criteria or insisting on a universal approach to measuring frailty, it is needed to move on to higher levels of care systems supporting their practical implementation, mapping the chosen frailty instrument to its specific role. This pragmatic study will equip older persons with awareness of their frailty status through community-based screening, allowing for timely stage-specific care to avoid deleterious outcomes. While older persons meeting frailty criteria will be referred for comprehensive geriatric assessment, pre-frail older persons will be targeted for multi-factorial exercise and nutritional intervention in the community to reverse the frailty trajectory. An over-arching aim will be to create a sustainable triaging system and early intervention programme that can be administered by trained members of the community. This will allow older persons to receive regular re-assessments in the community such that any transitions to a higher state of frailty may be captured and promptly addressed.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
This is a non-controlled prospective cohort study, recruiting community-dwelling older persons aged \>55 years, from various senior activity centres, day care and community centres in the North-East region of Singapore. A mobile community-based platform for frailty and physical fitness assessment will be anchored at the void decks of public housing blocks, senior activity centres (SACs), senior care centres (SCCs) or community clubs for accessibility. The platform will be maintained at each site for 2-3 consecutive weeks, and is managed by members of the multidisciplinary team, with the same site being re-visited at yearly intervals to allow follow-up. Each participant undergoes a multi-domain geriatric screen and physical fitness assessment, and will be triaged by physical frailty status for stage-specific care.
Written informed consent will be obtained from all participants, and ethics approval has been obtained from the Institutional Review Board of Singhealth.
Measures Multi-domain geriatric screen The multi-domain geriatric screen includes assessment of (i) socio-demographic characteristics (including social support network, socio-economic status, education and employment); (ii) mood as assessed using the 15-item Geriatric Depression Scale; (iii) cognitive performance using the locally validated modified Chinese version of Mini Mental State Examination (CMMSE); (iv) nutrition using the Mini Nutrition Assessment-Short Form (MNA-SF) and Subjective Global Assessment (SGA); (iv) physical activity level based on a structured questionnaire to assess the time spent on physical activities over the last 7 days; (v) functional performance using Barthel's Index for activities of daily living (ADLs) and Lawton and Brody's instrumental ADLs, as well as Life Space Questionnaire (LSQ) for functional mobility; (vi) quality of life on EuroQol 5 dimensions (EQ-5D-5L) questionnaire and a visual analogue scale; (vii) sarcopenia using SARC-F questionnaire enquiring ability to carry a heavy load, walking, rising from a chair, climbing stairs and falls, has been validated as a suitable tool for community screening for sarcopenia.
Frailty Assessment Frailty screening will be based on the 5-item FRAIL scale, which assesses for self-reported fatigue, resistance, ambulation, illnesses and loss of weight, to categorize participants as frail (score 3-5), pre-frail (1-2) or robust (0).
Physical frailty will be objectively assessed using modified Fried's criteria, with frailty defined by the presence of at least 3 and pre-frailty as 1-2 of 5 components - exhaustion, slow gait speed, weak grip strength, low body mass index (BMI\<18.5kg/m2) and low physical activity.
Grip strength will be measured using a JAMAR hand dynamometer, with 2 trials for each hand, and the maximum value will be used for analysis. Gait speed will be based on time taken to walk 10m at usual pace. Weakness (\<18kg for women and \<26 kg for men) and slowness (\<0.8m/s) will be defined using reference values from the Asian Working Group for Sarcopenia
Physical Fitness Tests The physical fitness test battery was modified from the Senior Fitness Test. Participants who report feeling unwell on pre-assessment screening will be exempt from fitness tests.
Lower body strength and power will be measured using the chair stand test, in which the participant will be instructed to rise as fast as possible from seated to a full standing position, while keeping the arms folded across the chest. Time taken to complete 5 chair stands as well as the number of full chair stands performed in 30 seconds will be recorded.
In addition to grip strength, upper limb dexterity will be assessed using the box-and-block test, in which participants pick up blocks and place them in the box on the other side across a barrier as quickly as possible. The number of blocks transferred in 1 minute will be recorded. 2 trials will be performed, one for each arm, and the better performance will be used for analysis.
Dual-task gait performance will be assessed by asking the participant to walk 10-metres while performing serial 2-step forward calculation and animal naming without specific instruction on task prioritization. Gait speed and number of correct calculations on the dual-task protocol will be recorded.
Upper and lower body flexibility will be assessed using the back-scratch and chair sit-and-reach tests respectively, with 2 trials for each test, and the better performance will be used for analysis. The back-scratch test is performed with the participant placing one hand behind the shoulder and the other hand up the middle of the back, fingers extended. The distance (cm) the middle fingers are short of touching (-) or overlapping (+) will be recorded. In the chair sit-and-reach test, participant sits on the edge of a chair with one leg extended in front while reaching forward with the hands toward the toes. The distance (cm) from the extended third finger to tip of toe (+ for beyond, and - for behind the toe) will be recorded.
Dynamic balance (agility) will be assessed on the Timed Up-and-Go Test, which requires the participant to stand from a seated position, walk as quickly as possible around a cone 3m ahead of the chair, and return to a fully seated position. The balance subtests of the Short Physical Performance Battery (SPPB) was also adopted, including side-by-side, semi-tandem and tandem standing.
Cardiorespiratory endurance will be evaluated using the 6-minute walk test (6MWT), along a walkway of at least 20m and with constant encouragement throughout the test. The total distance walked in 6 minutes will be recorded, and rest is permitted anytime during the test.
Each participant will be scored on the SPPB for a composite measure of physical performance, applying established cut-offs on the individual tests of gait speed, balance and chair stand.
Body Composition Participants will under Bioimpedance Analysis (BIA) (MC-780M, TANITA, Tokyo, Japan) for measurement of muscle mass.
Intervention for pre-frail older adults Pre-frail will be operationalized as the presence of 1-2 positive responses on FRAIL, or FRAIL score of 0 but with objective weak grip strength and/or slow gait speed. The latter takes into consideration the potential for under-reporting of symptoms on the FRAIL questionnaire.
Participants meeting operational criteria for pre-frailty will be enrolled in a group-based physical exercise and nutritional intervention programme, delivered over 4 months. The intervention will commence 3 months from the baseline screening.
Group-based, as opposed to traditional individual physiotherapy sessions, has been shown to boost older persons' motivation for participation and potentially addresses the social contribution to frailty.
Participants will undergo weekly 1-hr exercise sessions designed to challenge all major muscle groups with specific emphasis on strength training, in addition to gait, balance and endurance exercises, to target the major frailty elements of weakness and gait deficit, with demonstrated effectiveness for falls prevention in older adults. Upper limb strengthening exercises will be conducted through the use of therabands or free weights (e.g. bottled water) for resistance. The exercises will be made progressively more difficult over time (e.g. increasing the number of repetitions) according to group's progress, yet also catering for individual variability, under supervision of the physiotherapist. Endurance exercise will consist of outdoor walking. Targeting to each older adult's individual intensity level with progression as they improve ensures that the exercises remain physically challenging to provide sufficient stimulus. An individually prescribed structured home exercise programme with pictorials and explanations at the end of each session will be provided so that participants can continue with the exercises between sessions to achieve an optimal frequency of exercising at least three times a week, with a checklist to record adherence.
Nutritional intervention (6 group-based session) will be delivered with the aim of facilitating healthy eating habits to achieve adequate protein, energy, Vitamin D and fluid intake through regular foods and beverages without the need for nutritional supplements. Educating older adults to evaluate and adapt their nutritional intake, taking into consideration their dietary habits, can be expected to improve sustainability of effect and adherence. A group grocery-shopping trip will be conducted to provide guidance on choosing quality food within budget.
All participants will be followed up at 6-, 12- and 24-month. Participants enrolled in the intervention programme will have their physical performance measures at 3-month (immediate pre-intervention). Subsequent follow-up visits will be at the end of the 4-month intervention, 6- and 12-month post-intervention.
Written informed consent will be obtained from all participants, and ethics approval has been obtained from the Institutional Review Board of Singhealth.
Measures Multi-domain geriatric screen The multi-domain geriatric screen includes assessment of (i) socio-demographic characteristics (including social support network, socio-economic status, education and employment); (ii) mood as assessed using the 15-item Geriatric Depression Scale; (iii) cognitive performance using the locally validated modified Chinese version of Mini Mental State Examination (CMMSE); (iv) nutrition using the Mini Nutrition Assessment-Short Form (MNA-SF) and Subjective Global Assessment (SGA); (iv) physical activity level based on a structured questionnaire to assess the time spent on physical activities over the last 7 days; (v) functional performance using Barthel's Index for activities of daily living (ADLs) and Lawton and Brody's instrumental ADLs, as well as Life Space Questionnaire (LSQ) for functional mobility; (vi) quality of life on EuroQol 5 dimensions (EQ-5D-5L) questionnaire and a visual analogue scale; (vii) sarcopenia using SARC-F questionnaire enquiring ability to carry a heavy load, walking, rising from a chair, climbing stairs and falls, has been validated as a suitable tool for community screening for sarcopenia.
Frailty Assessment Frailty screening will be based on the 5-item FRAIL scale, which assesses for self-reported fatigue, resistance, ambulation, illnesses and loss of weight, to categorize participants as frail (score 3-5), pre-frail (1-2) or robust (0).
Physical frailty will be objectively assessed using modified Fried's criteria, with frailty defined by the presence of at least 3 and pre-frailty as 1-2 of 5 components - exhaustion, slow gait speed, weak grip strength, low body mass index (BMI\<18.5kg/m2) and low physical activity.
Grip strength will be measured using a JAMAR hand dynamometer, with 2 trials for each hand, and the maximum value will be used for analysis. Gait speed will be based on time taken to walk 10m at usual pace. Weakness (\<18kg for women and \<26 kg for men) and slowness (\<0.8m/s) will be defined using reference values from the Asian Working Group for Sarcopenia
Physical Fitness Tests The physical fitness test battery was modified from the Senior Fitness Test. Participants who report feeling unwell on pre-assessment screening will be exempt from fitness tests.
Lower body strength and power will be measured using the chair stand test, in which the participant will be instructed to rise as fast as possible from seated to a full standing position, while keeping the arms folded across the chest. Time taken to complete 5 chair stands as well as the number of full chair stands performed in 30 seconds will be recorded.
In addition to grip strength, upper limb dexterity will be assessed using the box-and-block test, in which participants pick up blocks and place them in the box on the other side across a barrier as quickly as possible. The number of blocks transferred in 1 minute will be recorded. 2 trials will be performed, one for each arm, and the better performance will be used for analysis.
Dual-task gait performance will be assessed by asking the participant to walk 10-metres while performing serial 2-step forward calculation and animal naming without specific instruction on task prioritization. Gait speed and number of correct calculations on the dual-task protocol will be recorded.
Upper and lower body flexibility will be assessed using the back-scratch and chair sit-and-reach tests respectively, with 2 trials for each test, and the better performance will be used for analysis. The back-scratch test is performed with the participant placing one hand behind the shoulder and the other hand up the middle of the back, fingers extended. The distance (cm) the middle fingers are short of touching (-) or overlapping (+) will be recorded. In the chair sit-and-reach test, participant sits on the edge of a chair with one leg extended in front while reaching forward with the hands toward the toes. The distance (cm) from the extended third finger to tip of toe (+ for beyond, and - for behind the toe) will be recorded.
Dynamic balance (agility) will be assessed on the Timed Up-and-Go Test, which requires the participant to stand from a seated position, walk as quickly as possible around a cone 3m ahead of the chair, and return to a fully seated position. The balance subtests of the Short Physical Performance Battery (SPPB) was also adopted, including side-by-side, semi-tandem and tandem standing.
Cardiorespiratory endurance will be evaluated using the 6-minute walk test (6MWT), along a walkway of at least 20m and with constant encouragement throughout the test. The total distance walked in 6 minutes will be recorded, and rest is permitted anytime during the test.
Each participant will be scored on the SPPB for a composite measure of physical performance, applying established cut-offs on the individual tests of gait speed, balance and chair stand.
Body Composition Participants will under Bioimpedance Analysis (BIA) (MC-780M, TANITA, Tokyo, Japan) for measurement of muscle mass.
Intervention for pre-frail older adults Pre-frail will be operationalized as the presence of 1-2 positive responses on FRAIL, or FRAIL score of 0 but with objective weak grip strength and/or slow gait speed. The latter takes into consideration the potential for under-reporting of symptoms on the FRAIL questionnaire.
Participants meeting operational criteria for pre-frailty will be enrolled in a group-based physical exercise and nutritional intervention programme, delivered over 4 months. The intervention will commence 3 months from the baseline screening.
Group-based, as opposed to traditional individual physiotherapy sessions, has been shown to boost older persons' motivation for participation and potentially addresses the social contribution to frailty.
Participants will undergo weekly 1-hr exercise sessions designed to challenge all major muscle groups with specific emphasis on strength training, in addition to gait, balance and endurance exercises, to target the major frailty elements of weakness and gait deficit, with demonstrated effectiveness for falls prevention in older adults. Upper limb strengthening exercises will be conducted through the use of therabands or free weights (e.g. bottled water) for resistance. The exercises will be made progressively more difficult over time (e.g. increasing the number of repetitions) according to group's progress, yet also catering for individual variability, under supervision of the physiotherapist. Endurance exercise will consist of outdoor walking. Targeting to each older adult's individual intensity level with progression as they improve ensures that the exercises remain physically challenging to provide sufficient stimulus. An individually prescribed structured home exercise programme with pictorials and explanations at the end of each session will be provided so that participants can continue with the exercises between sessions to achieve an optimal frequency of exercising at least three times a week, with a checklist to record adherence.
Nutritional intervention (6 group-based session) will be delivered with the aim of facilitating healthy eating habits to achieve adequate protein, energy, Vitamin D and fluid intake through regular foods and beverages without the need for nutritional supplements. Educating older adults to evaluate and adapt their nutritional intake, taking into consideration their dietary habits, can be expected to improve sustainability of effect and adherence. A group grocery-shopping trip will be conducted to provide guidance on choosing quality food within budget.
All participants will be followed up at 6-, 12- and 24-month. Participants enrolled in the intervention programme will have their physical performance measures at 3-month (immediate pre-intervention). Subsequent follow-up visits will be at the end of the 4-month intervention, 6- and 12-month post-intervention.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Frailty
Frailty Syndrome
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
Allocation Method
NA
Intervention Model
SINGLE_GROUP
This is a pre-post study design with a single group and no control arm. The study aims to screen 700 participants, of which, 220 pre-frail seniors to be recruited into the intervention programme.
Primary Study Purpose
SCREENING
Blinding Strategy
NONE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Pre-frail intervention
Pre-frail partiipants will undergo 4 month intervention consisted of group-based physical exercise and nutritional classes.
Intervention Type
BEHAVIORAL
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* any community-dwelling adult aged 55 and above
* able to ambulate independently (use of walking aids permitted)
* able to ambulate independently (use of walking aids permitted)
Exclusion Criteria
* For the pre-frail intervention programme, older adults with significant cognitive impairment, as defined using age- and education-adjusted local norms on the modified Chinese version of the Mini-Mental State Examination (CMMSE) will be excluded
Minimum Eligible Age
55 Years
Eligible Sex
ALL
Accepts Healthy Volunteers
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Sengkang General Hospital
OTHER
Sponsor Role
lead
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Responsibility Role
SPONSOR
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Laura Tay
Role: PRINCIPAL_INVESTIGATOR
Sengkang General Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Sengkang General Hospital
Singapore, , Singapore
Site Status
RECRUITING
Countries
Review the countries where the study has at least one active or historical site.
Singapore
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Laura Tay
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2018/2353
Identifier Type: -
Identifier Source: org_study_id