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Motivation for Exercise: A Mood-Based Focus

Motivation for Exercise: A Mood-Based Focus

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06706180
Enrollment
48
Registered
2024-11-26
Start date
2024-10-15
Completion date
2025-03-17
Last updated
2025-12-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise Motivation

Keywords

Exercise motivation, Exercise for mood

Brief summary

The goal of this study is to assess the effects of an exercise-related video on exercise motivation and adherence. Specifically, the researchers are studying whether an exercise-for-mood video increase levels of exercise motivation as compared to an exercise-for-fitness video.

Detailed description

This study is designed to evaluate two interventions for exercise motivation: an exercise-for-mood video and an exercise-for-fitness video. After screening to determine eligibility, participants will complete two virtual study appointments, scheduled 10-20 days apart. In Phase 1, participants will first consent to the study and complete the DASS-21, ASI-3, and EMI-2. Participants will then complete an interview-format 7-day Physical Activity Recall (7-day PAR) about their exercise over the past week. Participants are then randomized to either the Fitness or Mood video by the researcher and are assigned to watch the video while on the Zoom meeting, approximately 11 minutes long. After the video, participants complete two short questionnaires about the credibility and usefulness of the video they watched. Finally, participants are briefed on safe exercise habits and given a goal of moderate exercise 4 times per week. In the Phase 2 appointment, participants complete the EMI-2 and the 7-day PAR about their exercise over the past week. Participants are then debriefed on the intent of the study.

Interventions

OTHERExercise for Mood video

As per arm of the same name

OTHERExercise for Fitness video

As per arm of the same name

Sponsors

Boston University Charles River Campus
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Participants do not know that there are two motivational conditions. All outcomes are self-reported.

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* At least 18 years of age * Current PS101 student at Boston University * A score of 14 or higher on the Perceived Stress Scale (PSS) * Able to read English to provide informed consent * Familiarity with a computer keyboard and mouse or a touch screen device * Access to Zoom video conferencing software

Exclusion criteria

* Under age 18 * Known conditions prohibiting exercise adoption as identified by risk scores on the PAR-Q (a score of yes on one or more items) * Presence of anorexia nervosa or atypical anorexia nervosa, or recent (6 month) suicidal ideation * Score of 13 or lower on the Perceived Stress Scale (PSS)

Design outcomes

Primary

MeasureTime frameDescription
Exercise MotivationAssessed at Phase 1 appointment and Phase 2 appointment, scheduled 10-20 days apart.Exercise Motivations Inventory (EMI-2)

Secondary

MeasureTime frameDescription
Exercise adherenceRetrospective accounting of the past 7 days, assessed at Phase 1 appointment and Phase 2 appointment, scheduled 10-20 days apart.Adherence to an exercise goal of moderate-intensity exercise 4 times per week. Evaluated using the 7-day Physical Activity Recall (7-day PAR).
Mood During ExerciseAssessed at Phase 1 appointment and Phase 2 appointment, scheduled 10-20 days apartMood during most typical, intentional physical activity over the past week, evaluated on the Feeling Scale (FS)
Perceived Exertion during ExerciseAssessed at Phase 1 appointment and Phase 2 appointment, scheduled 10-20 days apartExertion during most typical, intentional physical activity over the past week, evaluated on the Ratings of Perceived Exertion scale (RPE)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026