NCT05360485

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2022

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 26, 2022

Completed
2 months until next milestone

Study Start

First participant enrolled

May 1, 2022

Completed
3 days until next milestone

First Posted

Study publicly available on registry

May 4, 2022

Completed
1.6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2024

Completed
Last Updated

October 9, 2024

Status Verified

March 1, 2024

Enrollment Period

1.6 years

First QC Date

February 26, 2022

Last Update Submit

October 7, 2024

Conditions

Outcome Measures

Primary Outcomes (2)

  • 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

  • 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 Outcomes (2)

  • Change in average active workday hours at follow-up

    5 days at baseline, 5 days post 1-month follow-up

  • Change in average workday MVPA minutes at follow-up

    5 days at baseline, 5 days post 1-month follow-up

Study Arms (2)

Fitbit-Only Self-Monitoring

ACTIVE COMPARATOR

Control 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).

Behavioral: Fitbit Self-Monitoring

MOV'D plus Fitbit Self-Monitoring

EXPERIMENTAL

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.

Behavioral: MOV'D (Move Often eVery Day)Behavioral: Fitbit Self-Monitoring

Interventions

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.

MOV'D plus Fitbit Self-Monitoring

All participants receive a Fitbit and are told to monitor their physical activity for the duration of the study period.

Fitbit-Only Self-MonitoringMOV'D plus Fitbit Self-Monitoring

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • 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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Stanford University School of Medicine

Stanford, California, 94305-7240, United States

Location

Related Publications (2)

  • Monteiro A, Moore J, Aikens R, Duckworth A, Gross JJ, Schwartz D, Baiocchi M, Prochaska JJ, Oppezzo M. A Work-Based, Fully Remote, and Peer-Supported Exercise Snack Behavior Change Intervention (MOV'D): Protocol for a Randomized Controlled Pilot Trial. JMIR Res Protoc. 2025 Aug 7;14:e64455. doi: 10.2196/64455.

  • Zamora AN, Zeitlin AB, Moore JB, Oppezzo M. Exploring Perceptions, Barriers, and Facilitators of Participation in an Exercise Snack Intervention Among U.S. Office Workers: Findings From a Pilot Study. Am J Health Promot. 2025 May 4:8901171251338217. doi: 10.1177/08901171251338217. Online ahead of print.

MeSH Terms

Conditions

Sedentary Behavior

Condition Hierarchy (Ancestors)

Behavior

Study Officials

  • Marily A. Oppezzo, PhD MS, RDN, DipACLM

    Stanford University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Model Details: This is preliminary efficacy, acceptability, and feasibility pilot with a randomized controlled design. The preliminary efficacy pilot 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). The 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 trial.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Instructor of Medicine

Study Record Dates

First Submitted

February 26, 2022

First Posted

May 4, 2022

Study Start

May 1, 2022

Primary Completion

December 1, 2023

Study Completion

January 1, 2024

Last Updated

October 9, 2024

Record last verified: 2024-03

Data Sharing

IPD Sharing
Will share

Will be shared upon request

Locations