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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT05360485
Other study ID # 60388
Secondary ID K01HL136702
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date May 1, 2022
Est. completion date September 2024

Study information

Verified date March 2023
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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 information / eligibility

Status Active, not recruiting
Enrollment 72
Est. completion date September 2024
Est. primary completion date September 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility 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 Exclusion Criteria: -

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
MOV'D (Move Often eVery Day)
The MOV'D 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.
Fitbit Self-Monitoring
All participants receive a Fitbit and are told to monitor their physical activity for the duration of the study period.

Locations

Country Name City State
United States Stanford University School of Medicine Stanford California

Sponsors (2)

Lead Sponsor Collaborator
Stanford University National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in average active workday hours at post-intervention 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 5 days at baseline, 5 days after 1 month treatment
Primary Change in average workday MVPA minutes at post-intervention Average minutes of moderate to vigorous minutes, or minutes above 3 METs per workday (of five) at 5 days at baseline, 5 days after 1 month treatment
Secondary Change in average active workday hours at 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 5 days at baseline, 5 days post 1-month follow-up
Secondary Change in average workday MVPA minutes at follow-up Average minutes of moderate to vigorous minutes, or minutes above 3 METs +per workday (of five) 5 days at baseline, 5 days post 1-month follow-up
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