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Schedule Intervention to Increase Sustainable Walking Activity in Midlife Working Adults

B

Brandeis University

Status

Completed

Conditions

Physical Activity

Treatments

Behavioral: Inconsistent contexts
Device: Accelerometer
Behavioral: Step goal
Behavioral: Consistent contexts

Study type

Interventional

Funder types

Other

Identifiers

NCT03272438
BrandeisU

Details and patient eligibility

About

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.

Full description

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. Participants will be randomly assigned to one of three conditions: consistent schedule, inconsistent schedule, no schedule. All participants will be provided with an accelerometer to measure their daily activity and as a behavioral support for our intervention and they will be given a step goal. The goal given to each individual will be to increase immediately their daily steps to a level based on recommended guidelines (e.g., Hill, Wyatt, Reed, and Peters, 2003). The investigators will test which version of the scheduling intervention is most successful for increasing and maintaining step counts. It is predicted that participants in the consistent schedule condition will increase their step count more than those participants in the no schedule control condition, and that they will maintain this activity for a longer period after the intervention period is complete than those participants in the inconsistent schedule condition.

Enrollment

149 patients

Sex

All

Ages

40 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 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)

Exclusion criteria

  • 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

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

149 participants in 3 patient groups

No schedule control
Active Comparator group
Description:
This 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.
Treatment:
Behavioral: Step goal
Device: Accelerometer
Consistent schedule condition
Experimental group
Description:
This 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.
Treatment:
Behavioral: Consistent contexts
Behavioral: Step goal
Device: Accelerometer
Inconsistent schedule condition
Active Comparator group
Description:
This 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.
Treatment:
Behavioral: Step goal
Device: Accelerometer
Behavioral: Inconsistent contexts

Trial contacts and locations

1

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Central trial contact

Margie Lachman, PhD; Jane Ebert, PhD

Data sourced from clinicaltrials.gov

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