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Functional Exercise and Nutrition Education Program for Older Adults (MoveStrong)

Primary Purpose

Chronic Disease, Frail, Diabetes Mellitus

Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Strength and Balance Training & Nutrition Education
Usual Care
Sponsored by
University of Waterloo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Chronic Disease focused on measuring Strength Training, Balance Training, Nutrition Education, Older adults, Frailty, Feasibility

Eligibility Criteria

60 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Speak English or attend with a translator;
  • ≥ 60 years;
  • FRAIL scale score ≥1;
  • Have ≥1 diagnosed chronic condition (i.e., diabetes, obesity, cancer (other than minor skin cancer), chronic lung disease, cardiovascular disease, congestive heart failure, hypertension, osteoporosis, arthritis, stroke, or kidney disease).

Exclusion Criteria:

  • Currently doing similar resistance exercise ≥2x/week;
  • In palliative care;
  • Not able to perform basic activities of daily living;
  • Cognitive impairment (e.g., unable to follow two-step commands);
  • Travelling >1 week during exposure;
  • Absolute exercise contraindications (i.e., if they select "no" to any question in the Get Active Questionnaire they must seek physician approval before exercising)

Sites / Locations

  • Chaplin Family YMCA
  • The Village of Arbour Trails
  • Village of Winston Park
  • A.R. Kaufman Family YMCA
  • Your Family Health Team

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Intervention

Control

Arm Description

At regular intervals (the "steps") one cluster (i.e., one site) is randomised to cross from the control to the intervention under evaluation. This process continues until all clusters have crossed over to be exposed to the intervention. At the end of the study there will be a period when all clusters are exposed. Four sites are cluster-randomized to implement MoveSTroNg at one of four start times, each three weeks apart.

Each cluster contributes observations under both control and intervention observation periods.

Outcomes

Primary Outcome Measures

Feasibility - Recruitment
Definition: Number recruited at end of rollout. The criterion for success is to recruit 10 participants at each of 4 sites.
Feasibility - Retention
Definition: Number retrained at post-rollout end. The criterion for success is 90% at rollout end.
Feasibility - Adherence
Definition: Percentage of individuals that attended exercise and nutrition sessions. The criterion for success is 70% or higher.

Secondary Outcome Measures

Body weight
Fried Frailty Index Components: We will measure the change in body weight with a calibrated scale. A change of 5% (greater or lower) in 1 year is considered worse.
10 Meter Walk Test
Fried Frailty Index Components: walking speed via the 10-meter walk test protocol. A change of 0.05 m/s is considered as a small meaningful change, while 0.13m/s is considered a substantial change.
Center for Epidemiological Study Depression Scale
Fried Frailty Index Components: fatigue/exhaustion via the Center for Epidemiologic Study Depression Scale-Fatigue Questions. The score ranges from 0-60 (higher scores reflect increased symptom severity)
Physical Activity Scale
Fried Frailty Index Components: lower physical activity via the CHAMPS Physical Activity Questionnaire for older adults. No score, but the recommended physical activity levels are 150 minutes of moderate to vigorous activity and 2 days of strength training of major muscle groups.
Grip Strength
Fried Frailty Index Components: weakness via the Jamar hand-held dynamometer
30 Second Chair Stand Test
We will use a chair with a straight back without arm rests (seat 17" high), and a stopwatch. This will assess leg strength and endurance. Scores range depending on age and sex (e.g., male 60 to 64, < 14 chair stands is considered below average, while a male 65 to 69, < 12 is below average).
4 Square Step Test
The Four Square Step Test is used to assess dynamic stability and the ability of the subject to step over low objects forward, sideways, and backward. For older adults > 15 seconds indicates increased risk of falls
EuroQol 5 dimension version 5-level (EQ-5D-5L)
The EuroQol 5 dimension version 5-level (EQ-5D-5L) measures quality of life using 5 dimensions, on a 5 point scale, where a higher point is considered better. The EuroQol 5 dimension version 5-level (EQ-5D-5L) also records the respondent's self-rated health on a 20 cm vertical, visual analogue scale with endpoints labelled 'the best health you can imagine' (100) and 'the worst health you can imagine' (0). This information can be used as a quantitative measure of health as judged by the individual respondents. A higher score indicates better quality of life
Automated Self-Administered 24-Hour (ASA24®) Dietary Assessment Tool
We will use the Automated Self-Administered 24-Hour (ASA24®) Dietary Assessment Tool to conduct interviewer administered diet recalls for 2 weekdays and 1 weekend day. Nutrient analysis is automated and will be used to quantify and compare protein and energy intakes at baseline and follow-up only. There is no scale to this section
Participant and provider experience
We will use a semi-structured interview guide to conduct exit interviews with each participant and kinesiologist. Interviews and training sessions will be audio-recorded and transcribed verbatim. Two researchers will perform thematic analyses to describe participant and provider experience and satisfaction, adaptations, and learning needs. There is no scale to this section
Adverse events
We will ask participants to report adverse events and falls, using Health Canada definitions. We will report serious and non-serious adverse events (total and attributable to intervention). There is no scale to this section
Resource use
We will use the Productivity and Activity Index questionnaire to assess indirect resource use over the last 6 weeks of the program.There is no scale to this section
Resource use
We will use the Health Utility Form to assess direct medical resource use over the last 6 weeks of the program. Direct medical costs will be measured using a closed and open-ended survey about their personnel, hospitalization, medications, rehabilitation, and test costs. This questionnaire also evaluates out of pocket expenses and transportation.There is no scale to this section

Full Information

First Posted
June 28, 2019
Last Updated
November 2, 2020
Sponsor
University of Waterloo
Collaborators
Canadian Institutes of Health Research (CIHR), City of Lakes family Health Team, Schlegel Villages and Research Institute for Aging, YMCA, Kinnect to Wellness
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1. Study Identification

Unique Protocol Identification Number
NCT04037436
Brief Title
Functional Exercise and Nutrition Education Program for Older Adults
Acronym
MoveStrong
Official Title
A Model for Delivering Strength Training and Nutrition Education for Older Adults (MoveStrong): A Pilot Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Completed
Study Start Date
September 24, 2019 (Actual)
Primary Completion Date
March 14, 2020 (Actual)
Study Completion Date
September 1, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Waterloo
Collaborators
Canadian Institutes of Health Research (CIHR), City of Lakes family Health Team, Schlegel Villages and Research Institute for Aging, YMCA, Kinnect to Wellness

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
There is strong evidence that specific types of exercise can improve health and physical function in older adults. While community exercise classes exist, many older adults with chronic conditions may need guidance from credentialed exercise professionals to ensure sufficient dose and progression and to address fears or low exercise self-efficacy. Furthermore, low protein intake among older adults is common and initiating exercise when nutrition is inadequate may cause weight loss and limit gains in muscle strength. The primary goal is to determine the feasibility of implementing the MoveSTroNg program under real-world conditions, measured through referral and recruitment to the program and study retention and adherence rates.
Detailed Description
The MoveStrong trial is a 1-year pilot closed cohort stepped wedge randomized control trial (RCT) to evaluate the feasibility of implementation of the MoveStrong program. This program includes a functional exercise and nutrition program that teaches older adults with chronic diseases how to perform functional resistance and balance exercises and promote adequate protein intake and nutrition. Four sites (1 Northern and 3 Southern Ontario sites) will be cluster-randomized to implement MoveStrong at one of four start times, each three weeks apart. The primary outcome will be to determine the feasibility of recruitment and referral from diverse settings (i.e., retirement homes, community centers, and family health teams) and establish the retention and adherence to the program. Secondary objectives will determine the following: What are the participant's and provider's experience with the MoveStrong program? What is the short-term responsiveness (i.e., ability to detect change) of frailty indicators (Fried Frailty Index components), protein intake, or quality of life? Who agrees to participate? What adaptations need to be made to MoveStrong, or study methods in each setting? What is the cost relative to the benefit? Is behaviour change maintained in the maintenance period? Our long term goal is to use the information from this project to develop, implement, and evaluate a sustainable, scalable and pragmatic model to deliver strength and balance training and promote adequate protein intake among older adults with chronic diseases.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Disease, Frail, Diabetes Mellitus, Cancer, Chronic Lung Disease, Cardiovascular Diseases, Congestive Heart Failure, Hypertension, Osteoporosis, Osteopenia, Arthritis, Stroke, Kidney Diseases
Keywords
Strength Training, Balance Training, Nutrition Education, Older adults, Frailty, Feasibility

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
We will use a closed cohort stepped wedge design at 4 sites (1 in Northern Ontario and 3 in Southern Ontario). In a stepped wedge, sites are cluster-randomized to implement MoveSTroNg at one of four start times, each three weeks apart.
Masking
None (Open Label)
Masking Description
Single (Outcomes Assessor)
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
At regular intervals (the "steps") one cluster (i.e., one site) is randomised to cross from the control to the intervention under evaluation. This process continues until all clusters have crossed over to be exposed to the intervention. At the end of the study there will be a period when all clusters are exposed. Four sites are cluster-randomized to implement MoveSTroNg at one of four start times, each three weeks apart.
Arm Title
Control
Arm Type
Other
Arm Description
Each cluster contributes observations under both control and intervention observation periods.
Intervention Type
Other
Intervention Name(s)
Strength and Balance Training & Nutrition Education
Intervention Description
Exercise:A kinesiologist-led twice-weekly program. Prior to attending the program, each attendee gets a 1:1 session with the kinesiologist to decide exercise starting levels. Group exercises start with a warm-up stepping game. Participants then perform 2 sets of 8 repetitions of each exercise, gradually progressing to an intensity of 3-8 repetitions maximum. Exercises include one each of a push, pull, squat, reach/press, lunge/step-up, lift and carry movement. After, there is a 10-minute group discussion to prompt making exercise routine at home. Nutrition:Two dietitian-led interactive group seminars to promote strategies to increase protein intake and sampling of protein-rich snacks and protein supplements. Seminar topics consider the cost to prepare high protein foods, the ability of retirement home residents to alter diet, how and why to spread protein intake through the day, how much protein is in their usual choices, and easy-to-consume protein-rich snacks.
Intervention Type
Other
Intervention Name(s)
Usual Care
Intervention Description
During periods when a site is not involved in the MoveSTroNg program, participants will continue with their usual care routine. Usual care routines should not involve strength and balance exercises.
Primary Outcome Measure Information:
Title
Feasibility - Recruitment
Description
Definition: Number recruited at end of rollout. The criterion for success is to recruit 10 participants at each of 4 sites.
Time Frame
1 month (August 1 to 31st, 2019)
Title
Feasibility - Retention
Description
Definition: Number retrained at post-rollout end. The criterion for success is 90% at rollout end.
Time Frame
Start of the program to 9 weeks
Title
Feasibility - Adherence
Description
Definition: Percentage of individuals that attended exercise and nutrition sessions. The criterion for success is 70% or higher.
Time Frame
18 weeks after the start of the program
Secondary Outcome Measure Information:
Title
Body weight
Description
Fried Frailty Index Components: We will measure the change in body weight with a calibrated scale. A change of 5% (greater or lower) in 1 year is considered worse.
Time Frame
Start of the program and 18 weeks after the start
Title
10 Meter Walk Test
Description
Fried Frailty Index Components: walking speed via the 10-meter walk test protocol. A change of 0.05 m/s is considered as a small meaningful change, while 0.13m/s is considered a substantial change.
Time Frame
Start of the program and every 6 weeks until the 18th week
Title
Center for Epidemiological Study Depression Scale
Description
Fried Frailty Index Components: fatigue/exhaustion via the Center for Epidemiologic Study Depression Scale-Fatigue Questions. The score ranges from 0-60 (higher scores reflect increased symptom severity)
Time Frame
Start of the program and every 6 weeks until the 18th week
Title
Physical Activity Scale
Description
Fried Frailty Index Components: lower physical activity via the CHAMPS Physical Activity Questionnaire for older adults. No score, but the recommended physical activity levels are 150 minutes of moderate to vigorous activity and 2 days of strength training of major muscle groups.
Time Frame
Start of the program and every 6 weeks until the 18th week
Title
Grip Strength
Description
Fried Frailty Index Components: weakness via the Jamar hand-held dynamometer
Time Frame
Start of the program and every 6 weeks until the 18th week
Title
30 Second Chair Stand Test
Description
We will use a chair with a straight back without arm rests (seat 17" high), and a stopwatch. This will assess leg strength and endurance. Scores range depending on age and sex (e.g., male 60 to 64, < 14 chair stands is considered below average, while a male 65 to 69, < 12 is below average).
Time Frame
Start of the program and every 6 weeks until the 18th week
Title
4 Square Step Test
Description
The Four Square Step Test is used to assess dynamic stability and the ability of the subject to step over low objects forward, sideways, and backward. For older adults > 15 seconds indicates increased risk of falls
Time Frame
Start of the program and every 6 weeks until the 18th week
Title
EuroQol 5 dimension version 5-level (EQ-5D-5L)
Description
The EuroQol 5 dimension version 5-level (EQ-5D-5L) measures quality of life using 5 dimensions, on a 5 point scale, where a higher point is considered better. The EuroQol 5 dimension version 5-level (EQ-5D-5L) also records the respondent's self-rated health on a 20 cm vertical, visual analogue scale with endpoints labelled 'the best health you can imagine' (100) and 'the worst health you can imagine' (0). This information can be used as a quantitative measure of health as judged by the individual respondents. A higher score indicates better quality of life
Time Frame
Start of the program and every 6 weeks until the 18th week
Title
Automated Self-Administered 24-Hour (ASA24®) Dietary Assessment Tool
Description
We will use the Automated Self-Administered 24-Hour (ASA24®) Dietary Assessment Tool to conduct interviewer administered diet recalls for 2 weekdays and 1 weekend day. Nutrient analysis is automated and will be used to quantify and compare protein and energy intakes at baseline and follow-up only. There is no scale to this section
Time Frame
Start of the program and every 6 weeks until the 18th week
Title
Participant and provider experience
Description
We will use a semi-structured interview guide to conduct exit interviews with each participant and kinesiologist. Interviews and training sessions will be audio-recorded and transcribed verbatim. Two researchers will perform thematic analyses to describe participant and provider experience and satisfaction, adaptations, and learning needs. There is no scale to this section
Time Frame
18 weeks after the start of the program
Title
Adverse events
Description
We will ask participants to report adverse events and falls, using Health Canada definitions. We will report serious and non-serious adverse events (total and attributable to intervention). There is no scale to this section
Time Frame
every 6 weeks until the 18th week after the start of the program
Title
Resource use
Description
We will use the Productivity and Activity Index questionnaire to assess indirect resource use over the last 6 weeks of the program.There is no scale to this section
Time Frame
Start of the program and every 6 weeks until the 18th week
Title
Resource use
Description
We will use the Health Utility Form to assess direct medical resource use over the last 6 weeks of the program. Direct medical costs will be measured using a closed and open-ended survey about their personnel, hospitalization, medications, rehabilitation, and test costs. This questionnaire also evaluates out of pocket expenses and transportation.There is no scale to this section
Time Frame
Start of the program and every 6 weeks until the 18th week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Speak English or attend with a translator; ≥ 60 years; FRAIL scale score ≥1; Have ≥1 diagnosed chronic condition (i.e., diabetes, obesity, cancer (other than minor skin cancer), chronic lung disease, cardiovascular disease, congestive heart failure, hypertension, osteoporosis, arthritis, stroke, or kidney disease). Exclusion Criteria: Currently doing similar resistance exercise ≥2x/week; In palliative care; Not able to perform basic activities of daily living; Cognitive impairment (e.g., unable to follow two-step commands); Travelling >1 week during exposure; Absolute exercise contraindications (i.e., if they select "no" to any question in the Get Active Questionnaire they must seek physician approval before exercising)
Facility Information:
Facility Name
Chaplin Family YMCA
City
Cambridge
State/Province
Ontario
Country
Canada
Facility Name
The Village of Arbour Trails
City
Guelph
State/Province
Ontario
ZIP/Postal Code
N1G 0C9
Country
Canada
Facility Name
Village of Winston Park
City
Kitchener
State/Province
Ontario
ZIP/Postal Code
N2E 3K1
Country
Canada
Facility Name
A.R. Kaufman Family YMCA
City
Kitchener
State/Province
Ontario
ZIP/Postal Code
N2G 3C5
Country
Canada
Facility Name
Your Family Health Team
City
Sudbury
State/Province
Ontario
ZIP/Postal Code
P3A 2T4
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
If requested we will consider sharing data. If raw data is shared, participant data will be deidentified.
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Functional Exercise and Nutrition Education Program for Older Adults

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