N/A
Completed N=11
Return to Everyday Activities in the Community and Home
Aging · Activity · Lifestyle
Source: ClinicalTrials.gov NCT02786394 ↗
Enrolled (actual)
11
Serious AEs
0.0%
Results posted
Apr 2022
Primary outcomePrimary: REACH Session Feedback — 5.94 score on a scale
Summary
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.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY REACH Session Feedback |
5.94 | — |
| SECONDARY Physical Activity Identity |
46.2 | — |
| SECONDARY Grit Score |
4.1 | — |
| SECONDARY Automaticity Subscale of the Self-Report Habit Index |
4.9 | — |
| SECONDARY Sedentary Behaviour |
— | — |
| SECONDARY Hourly Activity |
— | — |
| SECONDARY Step Count |
7954 | — |
| SECONDARY Number of REACH Sessions Attended |
5 | — |
Eligibility Criteria
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.
Data sourced from ClinicalTrials.gov (NCT02786394). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.