Schedule Intervention to Increase Sustainable Walking Activity in Midlife Working Adults
Using a Schedule Intervention to Increase Sustainable Walking Activity in Midlife
1 other identifier
interventional
149
1 country
1
Brief Summary
While people commonly understand that regular physical exercise conveys many health benefits, only 20% of U.S. adults take regular exercise and they have difficulty maintaining new healthy behaviors. The goal of this study is to use a planning intervention to help establish and maintain a daily step regimen in working midlife adults. The investigators will ask participants to plan when, where, and how to act on a daily walking goal in conjunction with a scheduling intervention to increase the chances that they will maintain this new regimen. The effectiveness of three different scheduling interventions will be compared.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Apr 2018
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 25, 2017
CompletedFirst Posted
Study publicly available on registry
September 5, 2017
CompletedStudy Start
First participant enrolled
April 13, 2018
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 24, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
July 24, 2019
CompletedFebruary 17, 2025
September 1, 2022
1.3 years
April 25, 2017
February 13, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Physical activity
Number of steps taken each day as measured on accelerometer
Daily for 9 weeks
Secondary Outcomes (2)
Measures of well being
Before and after intervention (5 weeks apart), and at followup (4 weeks later)
Physical activity self-efficacy and ease
Weekly for 4 weeks
Study Arms (3)
No schedule control
ACTIVE COMPARATORThis group will receive an accelerometer and daily step goal. They will monitor their steps over the 9 week duration of the study. They will also monitor their steps over the 9 week duration of the study. They will have the same level of contact as the other two conditions.
Consistent schedule condition
EXPERIMENTALThis group will receive an accelerometer and daily step goal. They will monitor their steps over the 9 week duration of the study. They will have the same level of contact as the other two conditions. In addition they will plan when, where, and how they will take steps in consistent contexts, i.e., that are very similar from day to day.
Inconsistent schedule condition
ACTIVE COMPARATORThis group will receive an accelerometer and daily step goal. They will monitor their steps over the 9 week duration of the study. They will have the same level of contact as the other two conditions. In addition they will plan when, where, and how they will take steps in inconsistent contexts, i.e., that vary from day to day.
Interventions
Participants use an accelerometer to monitor their steps activity
Participants are given a daily step goal to aim for
Participants plan to take steps in contexts that are similar from day to day
Participants plan to take steps in contexts that vary from day to day
Eligibility Criteria
You may qualify if:
- currently working 3 or more days (or 24 hours or more) per week;
- physically minimally active (as determined using the International Physical Activity Questionnaire (IPAQ)
You may not qualify if:
- a recent (within the past 6 months) cardiovascular event, or fall.
- anyone who already exercises regularly, 3 times a week or more for at least 30 minutes, will be excluded
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Brandeis University
Waltham, Massachusetts, 02453-2728, United States
Related Publications (1)
Hill JO, Wyatt HR, Reed GW, Peters JC. Obesity and the environment: where do we go from here? Science. 2003 Feb 7;299(5608):853-5. doi: 10.1126/science.1079857.
PMID: 12574618BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jane Ebert, PhD
Brandeis University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Masking Details
- Participants are not aware of whether they are in an experimental or control condition.
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor of Marketing
Study Record Dates
First Submitted
April 25, 2017
First Posted
September 5, 2017
Study Start
April 13, 2018
Primary Completion
July 24, 2019
Study Completion
July 24, 2019
Last Updated
February 17, 2025
Record last verified: 2022-09
Data Sharing
- IPD Sharing
- Will not share