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NCT06197243 · ClinicalTrials.gov registry record · NA
Augmenting Benzodiazepine Receptor Agonist Deprescribing With Acupuncture and Yoga Among Older Adults
A NA study of Anxiety and Insomnia, sponsored by Vanderbilt University Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 23
- Enrollment target
- 1
- Study location
NCT06197243 is a NA study of Anxiety and Insomnia that has completed, run by Vanderbilt University Medical Center. The registered enrollment target is 23 participants, below the 440-participant average among 364 other Anxiety trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06197243, a NA study of Anxiety and Insomnia, has completed, sponsored by Vanderbilt University Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 23 participants
- Enrollment target
- 1
- Study location
Study Summary
The main purpose of this 12-week study is to see if a new combination of treatments can help older adults reduce benzodiazepine or related medication use. The treatment combination consists of 1) medical provider visits to gradually reduce the medication dose over 12 weeks, 2) acupuncture treatments, and 3) private yoga classes. Participants will be offered weekly visits for 12 weeks to receive combined treatments. Participants will be provided surveys before, during, and after the study to learn about their experience of the treatments. At the end of the study, participants will be invited to participate in a focus group to learn about their experience in the study.
Conditions Studied
Interventions
- OTHER Acupuncture
- OTHER Yoga
- OTHER Deprescribing
Study Locations (1)
Tennessee
- Osher Center for Integrative Health at Vanderbilt - Nashville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 23 participants |
| Start Date | 2023-12-14 |
| Est. Completion | 2025-05-23 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06197243
The ClinicalTrials.gov registry entry for NCT06197243 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 23 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 440-participant average among 364 other Anxiety trials with a reported enrollment target (95% lower). The listed sponsor is Vanderbilt University Medical Center, which has 677 total studies on file at ClinicalTrials.gov.
The record links to 4 conditions, with Anxiety appearing as the primary indexed condition, and to 3 interventions - of which Acupuncture is the first listed.
NCT06197243 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.
Frequently Asked Questions
What is clinical trial NCT06197243 about?
NCT06197243 is a clinical study titled "Augmenting Benzodiazepine Receptor Agonist Deprescribing With Acupuncture and Yoga Among Older Adults". The main purpose of this 12-week study is to see if a new combination of treatments can help older adults reduce benzodiazepine or related medication use. The treatment combination consists of 1) medical provider visits to gradually reduce the medication dose over 12 weeks, 2) acupuncture treatments...
What is the current status of trial NCT06197243?
This trial is currently completed. It is a NA study. The enrollment target is 23 participants. The study started on 2023-12-14. Estimated completion is 2025-05-23.
What conditions does trial NCT06197243 study?
This clinical trial studies the following conditions: Anxiety, Insomnia, Benzodiazepine, Deprescription.
What interventions are being tested in trial NCT06197243?
The interventions under investigation include: Acupuncture (OTHER), Yoga (OTHER), Deprescribing (OTHER).
Who is sponsoring clinical trial NCT06197243?
This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06197243 being conducted?
This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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