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Peer Motivation Coaches, Social Media-based Support Group, and Behavior Change Strategies to Decrease Prolonged Sitting and Increase Moderate Exercise Snacks

Not Applicable
Completed
Conditions
Physical Inactivity
Sedentary Behavior
Interventions
Behavioral: Fitbit Self-Monitoring
Behavioral: MOV'D (Move Often eVery Day)
Registration Number
NCT05360485
Lead Sponsor
Stanford University
Brief Summary

The MOV'D (Move Often eVery Day) intervention is a remotely-delivered, peer-supported intervention that delivers exercise snack (2-5 minutes of moderate to vigorous activity) and behavior change technique (BCT) videos to a private social media support group with the goal of interrupting prolonged sitting at work with MVPA minutes.

The preliminary efficacy, feasibility, and acceptability trial will test the effects of MOV'D, a socially-supported, evidence-based behavior change technique educational and behavioral intervention to increase the number of active hours (an indirect measure of prolonged sitting bouts) (Hypothesis 1) and number of MVPA minutes (Hypothesis 2). This pilot will gather important estimates of the effect sizes, the variance, and covariance of the primary outcomes to calculate the sample size needed to power a larger fully powered RCT.

Detailed Description

Prolonged sitting and inadequate moderate to vigorous intensity physical activity (MVPA) are pervasive risk factors for cardiovascular disease (CVD). Recent research has shown that some benefits of moderate to vigorous physical activity can be accrued in motivationally accessible short, 2-5 minute bouts throughout the day rather than needing to be a single, longer, continuous bout. The MOV'D intervention is a novel, remotely-delivered, social-media-based intervention to interrupt prolonged sitting with short bouts of MVPA, compared with a Fitbit-only control. The investigators will randomly assign participants to either MOV'D or a Fitbit only control for one month, with a one-month follow-up, to compare immediate and prolonged effects of treatment on number of workday hours with activity break and number of MVPA minutes.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
72
Inclusion Criteria
  • have smartphone with internet capabilities
  • spend more than 55% of time sedentary at work
  • English literacy
  • safe to exercise, assessed by the Physical Activity Readiness Questionnaire (PAR-Q)
  • full-time employee at sedentary job
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Exclusion Criteria
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Fitbit-Only Self-MonitoringFitbit Self-MonitoringControl participants will be sent a Fitbit and study-provided account and will self-monitor physical activity for the duration of the study period (2 months).
MOV'D plus Fitbit Self-MonitoringMOV'D (Move Often eVery Day)Treatment participants will be sent a Fitbit and study-provided account, and assigned to a private, study-created Twitter support group of 10 participants. Within the private group of 10, each participant is also further paired with a peer to be that person's peer coach, setting weekly exercise snack goals and practicing behavior change techniques.
MOV'D plus Fitbit Self-MonitoringFitbit Self-MonitoringTreatment participants will be sent a Fitbit and study-provided account, and assigned to a private, study-created Twitter support group of 10 participants. Within the private group of 10, each participant is also further paired with a peer to be that person's peer coach, setting weekly exercise snack goals and practicing behavior change techniques.
Primary Outcome Measures
NameTimeMethod
Change in average active workday hours at post-intervention5 days at baseline, 5 days after 1 month treatment

Average hours with \>2 min of MVPA (Moderate to Vigorous Physical Activity) or 250 steps between 8 AM - 7 PM per workday (of five); proxy for prolonged sitting time

Change in average workday MVPA minutes at post-intervention5 days at baseline, 5 days after 1 month treatment

Average minutes of moderate to vigorous minutes, or minutes above 3 METs per workday (of five) at

Secondary Outcome Measures
NameTimeMethod
Change in average active workday hours at follow-up5 days at baseline, 5 days post 1-month follow-up

Average hours with \>2 min of MVPA or 250 steps between 8 AM - 7 PM per workday (of five); proxy for prolonged sitting time

Change in average workday MVPA minutes at follow-up5 days at baseline, 5 days post 1-month follow-up

Average minutes of moderate to vigorous minutes, or minutes above 3 METs +per workday (of five)

Trial Locations

Locations (1)

Stanford University School of Medicine

🇺🇸

Stanford, California, United States

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