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CompletedNCT05217589Updated Oct 16, 2026

The Influence of Different Mood States and Emotions on the Physiologic, Metabolic, and Perceptual Responses to Feeding Before Exercise

An interventional study of Funny/Amusing Video Clips and Horror/Scary Video Clips in Other Gastrointestinal Disorders and Cramp, Abdominal, sponsored by Old Dominion University. Completed at 1 site in United States. Open to participants aged 18 Years to 55 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-16.

Sponsored by Old Dominion University · Not applicable, Interventional, and Basic science

Updated Oct 16, 2026Now CompletedPrimary completion moved+2 moreGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
28
Allocation
Randomized
Ages
18 Years to 55 Years
Sex
All
01

Study summary

Many athletes anecdotally report modifying their nutritional intake before competition in order to avoid gut problems, but no studies have evaluated whether emotional state impacts tolerance to pre-exercise feeding. Therefore, this study will use movie clips (stressful, horror, and funny/amusing) to induce different mood states and emotions, which will be followed by ingestion of food before endurance running on a treadmill. In addition, metabolic and physiologic responses to mood induction will be evaluated.

02

Conditions studied

  • Other Gastrointestinal Disorders
  • Cramp, Abdominal

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03

In context

Colic

127 studies on the registry are indexed under Colic; 18 are open to participants now.

This study's enrollment of 28 is below the median of 76 across 110 interventional studies indexed under Colic.

Browse Colic studies →

Lead sponsor

Old Dominion University is the lead sponsor of 27 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  1. Aged 18 to 55 years
  2. Able to run for 30 min at a moderate-to-vigorous intensity without stopping
  3. No diagnosis or signs/symptoms of cardiovascular disease (CVD) or metabolic disorders
  4. Currently physically active (at least 3 days/week of exercise at a moderate or higher intensity)
  5. No visual or hearing impairments interfering with ability to see and hear video clips
  6. No allergies to ingredients in Boost drink

Exclusion criteria

Exclusion Criteria:

  1. Aged \<18 or >55 years
  2. Unable to run for 30 min at a moderate-to-vigorous intensity without stopping
  3. A diagnosis or signs/symptoms of CVD or metabolic disorders
  4. Currently physically inactive (\< 3 days/week of exercise at a moderate or higher intensity)
  5. Visual or hearing impairments interfering with ability to see and hear video clips
  6. Allergies to ingredients in Boost drink
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
28 participants (actual)

Study arms

  • Experimental
    Funny/Amusing Video Clips

    Participants will watch 5-7-min video clips that are meant to be funny/amusing

    Other: Funny/Amusing Video Clips

  • Experimental
    Horror/Scary Video Clips

    Participants will watch 5-7-min video clips that are meant to be scary

    Other: Horror/Scary Video Clips

  • Experimental
    Thrilling/Suspenseful Video Clips

    Participants will watch 5-7-min video clips that are meant to be thrilling/suspenseful

    Other: Thrilling/Suspenseful Video Clips

Interventions

  • OtherFunny/Amusing Video Clips

    Participants watch 5-7 minutes of video clips that are funny/amusing in nature

  • OtherHorror/Scary Video Clips

    Participants watch 5-7 minutes of video clips that are scary in nature

  • OtherThrilling/Suspenseful Video Clips

    Participants watch 5-7 minutes of video clips that are thrilling/suspenseful in nature

06

What researchers measure

Primary outcomes

  1. Total exercise gastrointestinal symptom burden

    The severity of several gastrointestinal symptoms will be assessed on a validated 0-10 scale. Ratings will be collected every 5 minutes during a 30-minute treadmill jogging/running test. Scores from every 5-minute collection will be summed to calculate total GI symptom scores.

    Time frame: Total GI symptom burden over a 30-minute jogging/running protocol.

  2. Change in emotion ratings

    Anxiety, fear, happiness, amusement, disgust, sadness, and anger on a 0-9 Likert scale. Emotions will be assessed before watching video clips and immediately after watching video clips.

    Time frame: Change in emotion ratings between immediately pre-video and immediately post-video.

Secondary outcomes

  1. Change over time in exercise heart rate

    Heart rate will be measured with a chest-strap (Polar) monitor.

    Time frame: Heart rate will be measured throughout a 30-minute treadmill jogging/running test. Change over time will be evaluated using mixed ANOVA.

  2. Substrate use

    Carbohydrate and fat oxidation rates will be estimated from the volumes of oxygen consumption and carbon dioxide production during exercise

    Time frame: Carbohydrate and fat oxidation rates will be measured during the last 5 min of a 30-minute treadmill jogging/running test.

  3. Feeling Scale

    The Feeling Scale is a bipolar numerical rating scale ranging from -5 to +5, with descriptors of "very bad" at -5, "neutral" at 0, and "very good" at +5.

    Time frame: Ratings on the Feeling Scale will be measured at rest before watching video clips and throughout (every 5 min) a subsequent 30-minute treadmill jogging/running test.

  4. Fatigue Scale

    The Fatigue Scale is Likert-type scale that ranges from 0 (Not Fatigued at All) to 10 (Total Fatigue).

    Time frame: Ratings on the Fatigue Scale will be measured at rest before watching video clips and throughout (every 5 min) a subsequent 30-minute treadmill jogging/running test.

  5. Heart rate post-video

    Heart rate will be measured with a chest-strap (Polar) monitor.

    Time frame: Heart rate will be recorded immediately after videos are viewed.

07

Study locations

1 site
  • Human Performance Laboratory
    Norfolk, Virginia 23529, United States
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

1 registry update since Sep 25, 2026
Status
Recruiting→Completed
changed Oct 16, 2026
Primary completion
Dec 1, 2025→Apr 2, 2026 (actual)
Oct 16, 2026
Study completion
Dec 31, 2025→Apr 2, 2026 (actual)
Oct 16, 2026
Enrollment
90 (estimated)→28 (actual)
Oct 16, 2026
Show all 1 update
  1. Oct 16, 2026
    Recruiting→Completed
    Primary completion Dec 1, 2025→Apr 2, 2026 (now actual)
    Study completion Dec 31, 2025→Apr 2, 2026 (now actual)
    Enrollment 90 (estimated)→28 (actual)
    + 5 other changes: verification date, oversight details, contact details, site details and index terms

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT05217589
Lead sponsor
Old Dominion University
Responsible party
Patrick Wilson, PhD (Associate Professor of Exercise Science, Old Dominion University) — Principal investigator
First posted
Feb 1, 2022
Start date
Apr 1, 2022
Primary completion
Apr 2, 2026
Completion
Apr 2, 2026
Last update
Oct 16, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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