- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04651751
Exercise Habit & MPAC
November 25, 2020 updated by: Ryan Rhodes, University of Victoria
Facilitating an Exercise Habit and Identity Via the Multi-Process Action Control Model- A Randomized-Controlled Trial
The limitations of applying social cognitive models to understand physical activity (PA) have led to the emergence of several new PA models within the past decade.
The Multi-Process Action Control (M-PAC) is a comprehensive PA model that proposes intention is established from outcome expectations, perceived capability, and opportunity, then the success of translating this to behavior depends on affective judgments and behavioral-regulation.
Over time, M-PAC proposes that behavior is can become maintained through the formation of identity and habit.
The purpose of this study was to investigate the trajectory of change of these M-PAC constructs across time in a randomized controlled trial.
Participants (n=85) were inactive new gym members and were randomized into a control (n=41) or intervention (n=44) group.
The intervention group attended a workshop and received a booster phone call follow-up at week four.
Measures for both groups included accelerometry and M-PAC at baseline and eight week follow-up.
Study Overview
Status
Completed
Conditions
Study Type
Interventional
Enrollment (Actual)
85
Phase
- Not Applicable
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
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- adults 18-65
- new gym members
- exercising < 150 minutes/week at a moderate to vigorous level
Exclusion Criteria:
- not affiliated with a gym or recreation center
- exercising > 150 minutes/week at a moderate to vigorous level
- clinical health conditions (assessed by the PAR-Q)
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: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: Control
No Intervention: Control Participants exercised on their own without receiving any instructions.
|
|
|
Experimental: Intervention
Those who were randomized into the intervention group attended a workshop where the PI delivered a presentation that focused on establishing a preparatory exercise habit by using the M-PAC approach and proposed habit model.
Participants were then provided with instructions on completing their exercise plan sheet.
|
Participants attended a workshop which consisted of a presentation and an exercise planning exercise.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
GT3X+ Actigraph Activity Monitors (for measuring physical activity)
Time Frame: Baseline to 8 weeks
|
Participants wear accelerometers for one week at baseline and at week eight to record their physical activity.
|
Baseline to 8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
1.Self-Report Behavioural Automaticity Index (self report, survey question
Time Frame: Baseline, week four, week eight
|
The Self-Report Behavioral Automaticity Index (SRBAI) was used to assess preparatory habit.
The SRBAI consists of 4 items on a 5-point Likert scale with 1 being strongly disagree to 5 being strongly agree.
The question stem stated ''When I prepare to exercise…'' which was then followed by four items on the scale: ''I do it without having to consciously remember'', ''I do it automatically'', ''I do it without thinking'', and ''I start before I realize I am doing it''.
|
Baseline, week four, week eight
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Environmental Cues (self report, survey question)
Time Frame: Baseline, week four, week eight
|
The following item was used to assess if participants implemented the use of cues: "I use cues at home to remind me to exercise (e.g.
placing a water bottle on my desk or gym clothes on the bed).
The item was rated on a five point Likert scale which ranged from "1=strongly disagree" to "5= strongly agree".
|
Baseline, week four, week eight
|
|
Temporal Consistency (self report, survey question)
Time Frame: Baseline, week four, week eight
|
The item was worded "How consistently do you exercise at the same time each day?
(e.g., exercising every morning at 7 am, or exercising daily after supper)".
The question was asked on a five point Likert scale which range from "1=not consistent at all" to "5=very consistent".
|
Baseline, week four, week eight
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Ryan E Rhodes, PhD, University of Victoria
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
January 1, 2015
Primary Completion (Actual)
June 1, 2015
Study Completion (Actual)
June 1, 2015
Study Registration Dates
First Submitted
November 17, 2020
First Submitted That Met QC Criteria
November 25, 2020
First Posted (Actual)
December 3, 2020
Study Record Updates
Last Update Posted (Actual)
December 3, 2020
Last Update Submitted That Met QC Criteria
November 25, 2020
Last Verified
November 1, 2020
More Information
Terms related to this study
Other Study ID Numbers
- AT956
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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