- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02786394
Return to Everyday Activities in the Community and Home (REACH)
May 8, 2023 updated by: Maureen C. Ashe, University of British Columbia
REACH Lifestyle Program for Older Adults
The purpose of this study is to test feasibility for the delivery and perceptions of a lifestyle model for middle-aged and older adults by involving participants in its development.
The goal of the program is to reduce sedentary behaviour, increase physical activity, and increase strength and balance.
An optional walking program will be run in parallel to emphasize the importance of moving more.
Participants will be asked to fill out questionnaires on course delivery, content and effect throughout the program and 2-3 recorded interviews throughout the study.
We will collect measurements of physical performance before and after the program.
Study Overview
Detailed Description
This study aims to describe the delivery of a lifestyle model for older adults.
Return to Everyday Activities in the Community and Home (REACH) is a health promotion program aimed at middle-aged and older adults.
The goal of REACH is to reduce sedentary behaviour, increase physical activity, and increase strength and balance.
The REACH program is comprised of six sessions which include evidence-based education, behaviour change theory, and activity instruction.
REACH also teaches goal setting techniques, mindfulness, and encourages active community engagement.
In this study we are running the REACH program for women aged 55 and older alongside a supplementary optional walking program run by SportMedBC.
We will gather pre- and post-intervention measures of program perceptions, delivery psychological variables and physical performance outcomes.
We will also collect participant feedback about course delivery, content and effect throughout the program.
This study will allow us to describe the delivery strategies of REACH and involve the participants in the development of the REACH program.
The optional walking program will emphasize the importance of increasing daily physical activity.
Study Type
Interventional
Enrollment (Actual)
11
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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British Columbia
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Vancouver, British Columbia, Canada, V5Z 1M9
- Centre for Hip Health and Mobility
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
55 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Participants included will be women aged 55 and older.
- Participants must speak English.
- Participants must be able to walk a minimum of four city blocks, climb a flight of stairs and take part in a physical activity and walking program.
- Participants must be cleared by a health care professional to participate using the Physical Activity Readiness Questionnaire for Everyone (Par-Q+) assessment to determine if they are physically able to take part in the activity program.
Exclusion Criteria:
- Individuals will be excluded if they are men, under the age of 55 and/or do not speak English.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: REACH Participant Course
This study will run twice a week over 6 weeks with 6 REACH sessions optional walking program sessions.
The optional walking program will be run by SportMedBC and may consist of one or more educational sessions (e.g., nutrition).
Each REACH session introduces new topics, strength and balance activities and home practices which progressively build on each other.
We will ask participants to provide feedback after each session, and in two to three 30 minutes recorded interviews (in-person or over the telephone) at the end of the study.
|
REACH is a lifestyle intervention program which aims to reduce sedentary behaviour, increase physical activity, and increase strength and balance.
The REACH program is comprised of six sessions which include evidence-based education, behaviour change theory, and activity instruction.
REACH also teaches goal setting techniques, mindfulness, and encourages active community engagement.
In this study we are running the REACH program for women aged 55 and older alongside a supplementary optional walking program run by SportMedBC.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
REACH Session Feedback
Time Frame: 6 weeks
|
We will ask participants to report feedback and experience following each REACH session.
As this was a pilot study we wanted to capture participants' perceptions of the program.
When appropriate, we adjusted the content/delivery in consultation with participants.
We also asked participants to rate their overall experience with REACH [1 (low) - 7 (high)].
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6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Physical Activity Identity
Time Frame: 6 weeks
|
A questionnaire will be administered at the beginning and end of the REACH sessions to determine how the participant identifies themselves with regard to physical activity.
The minimum score is 9 and the maximal score is 63; the higher the score the better.
|
6 weeks
|
|
Grit Score
Time Frame: 6 weeks
|
A questionnaire will be used to determine how the participant perceives their ability to stick with (follow through on) projects or goals.
The higher the score the better.
Scores range from 1 (not like me to) to 5 (very much like me).
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6 weeks
|
|
Automaticity Subscale of the Self-Report Habit Index
Time Frame: 6 weeks
|
A questionnaire will be administered to determine the participant's level of automaticity for physical activity.
Scores are based on a 7-point Likert scale (1=strongly disagree- 7=strongly agree).
In other words, participants rate how "automatic" their behavior is for physical activity.
|
6 weeks
|
|
Sedentary Behaviour
Time Frame: weekly for 6 weeks
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We will request participants record their sedentary behaviour data from activity monitors.
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weekly for 6 weeks
|
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Hourly Activity
Time Frame: weekly for 6 weeks
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We will request participants to record their hourly activity (number of hours active per day) data from activity monitors.
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weekly for 6 weeks
|
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Step Count
Time Frame: weekly for 6 weeks
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We will request participants to record their daily step count data from activity monitors.
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weekly for 6 weeks
|
|
Number of REACH Sessions Attended
Time Frame: weekly for 6 weeks
|
Number of REACH sessions attended during the project.
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weekly for 6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Maureen Ashe, PhD, University of British Colubia
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2016
Primary Completion (Actual)
June 1, 2016
Study Completion (Actual)
June 1, 2016
Study Registration Dates
First Submitted
May 18, 2016
First Submitted That Met QC Criteria
May 25, 2016
First Posted (Estimate)
June 1, 2016
Study Record Updates
Last Update Posted (Actual)
May 10, 2023
Last Update Submitted That Met QC Criteria
May 8, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- H16-00670
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
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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