CompletedNot Applicable

Brain-Gut Yoga for Functional Dyspepsia and Gastroparesis (FD-GP)

United States10 participantsStarted 2025-06-18

Plain-language summary

The purpose of this research study is to assess whether using a yoga-based intervention in practice is feasible (possible) and acceptable to patients with Functional Dyspepsia and/or Gastroparesis (FD-GP).

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 18 years and older * Functional Dyspepsia or Gastroparesis (FP or GP) diagnosed by a physician using standard criteria * Signed, written consent Exclusion Criteria: * Co-morbid Gastrointestinal or related disorders documents in the medical record: celiac disease, inflammatory Bowel Disease(active), gastrointestinal obstruction (if current in the last 6 months), any GI surgery within the last 6 months), chronic pancreatitis or any pancreatic or biliary disease, cirrhosis or any chronic liver disease other than metabolic associated hepatic disease (MASH), any malignancy (except skin cancer already resected and surgically in remission) * A positive screen for the following: current psychotic symptoms, elevated suicide risk, active eating disorder, cognitive impairment, current harmful alcohol or substance use * Does not understand English * Underwent a regular yoga or other mediative movement practice (tai chi or qi gong) in the past 6 month

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Screening Rate

Timeframe: Week 0

Recruitment Rate

Timeframe: Week 0

Retention Rate

Timeframe: Week 2

Adherence Rate

Timeframe: Week 2

Assessment Process Time

Timeframe: Week 2

Acceptability of Intervention Score

Timeframe: Week 2

Client Satisfaction Questionnaire Score

Timeframe: Week 2

Intervention Usability Scale Score

Timeframe: Week 2

Trial details

NCT IDNCT06732453

SponsorWake Forest University Health Sciences

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-06-03

View on ClinicalTrials.gov More Functional Dyspepsia trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Screening Rate

Timeframe: Week 0

Recruitment Rate

Timeframe: Week 0

Retention Rate

Timeframe: Week 2

Adherence Rate

Timeframe: Week 2

Assessment Process Time

Timeframe: Week 2

Acceptability of Intervention Score

Timeframe: Week 2

Client Satisfaction Questionnaire Score

Timeframe: Week 2

Intervention Usability Scale Score

Timeframe: Week 2