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NCT03572153 · ClinicalTrials.gov registry record · NA
A Mind-Body Intervention for Hot Flash Management
A NA study, sponsored by Baylor University.
- Completed
- Registry status
- NA
- Development phase
- 250
- Enrollment target
NCT03572153: Completed NA study, sponsored by Baylor University.
NCT03572153 is a NA study that has completed, run by Baylor University. The registered enrollment target is 250 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03572153, a NA study, has completed, sponsored by Baylor University.
- COMPLETED
- Registry status
- NA
- Development phase
- 250 participants
- Enrollment target
Study Summary
The long-term goal of this program of research is to determine safe and effective non-hormonal interventions for menopausal symptoms. The main goal of this study is to evaluate whether self-administered hypnosis can be used to significantly reduce hot flashes more than self-administered white noise hypnosis over 6 weeks of home practice. The investigators are also examining the impact of each hypnosis group on sleep, anxiety, perceived and measured stress, heart rate variability, and daily activities.
Primary Outcome
Participants completed the Hot Flash Daily Diary (Sloan et al., 2001) every day for 6 weeks to measure the daily frequency and severity (mild, moderate, severe, and very severe) of hot flashes. A total hot flash score was calculated for each participant (product of frequency x severity) after severity ratings were assigned a point value as follows: * mild = 1 * moderate = 2 * severe = 3 * very severe = 4 The hot flash score was then calculated by multiplying the participants' frequency and seve
Interventions
- BEHAVIORAL Self-Administered Hypnosis
- BEHAVIORAL Self-Administered White Noise Hypnosis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 250 participants |
| Start Date | 2019-03-04 |
| Est. Completion | 2024-02-16 |
| Phase | NA |
What the finished NCT03572153 record still lists
NCT03572153 is an interventional study that assigns participants to a tested intervention. The registered 250 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (82% lower).
The record links to 0 conditions, and to 2 interventions - of which Self-Administered Hypnosis is the first listed.
NCT03572153 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03572153 about?
NCT03572153 is a clinical study titled "A Mind-Body Intervention for Hot Flash Management". The long-term goal of this program of research is to determine safe and effective non-hormonal interventions for menopausal symptoms. The main goal of this study is to evaluate whether self-administered hypnosis can be used to significantly reduce hot flashes more than self-administered white noise ...
What is the current status of trial NCT03572153?
This trial is currently completed. It is a NA study. The enrollment target is 250 participants. The study started on 2019-03-04. Estimated completion is 2024-02-16.
What interventions are being tested in trial NCT03572153?
The interventions under investigation include: Self-Administered Hypnosis (BEHAVIORAL), Self-Administered White Noise Hypnosis (BEHAVIORAL).
Who is sponsoring clinical trial NCT03572153?
This trial is sponsored by Baylor University, which has 33 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03572153's enrollment target sits among peer trials
250 410th of 2000 higher than 1,567 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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