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NCT03198039 · ClinicalTrials.gov registry record · NA
Guided Meditation as an Adjunct to Enhance Postoperative Recovery
A NA study of Feasibility of a Meditation Program Perioperatively, sponsored by Beth Israel Deaconess Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 29
- Enrollment target
- 1
- Study location
NCT03198039: Completed NA study of Feasibility of a Meditation Program Perioperatively, sponsored by Beth Israel Deaconess Medical Center.
NCT03198039 is a NA study of Feasibility of a Meditation Program Perioperatively that has completed, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 29 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03198039, a NA study of Feasibility of a Meditation Program Perioperatively, has completed, sponsored by Beth Israel Deaconess Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 29 participants
- Enrollment target
- 1
- Study location
Study Summary
The primary purpose of this trial is to test the feasibility of implementing a meditation program in the perioperative period.
Primary Outcome
In this descriptive, feasibility study, evaluation of feasibility will include adherence to meditation intervention (total number of sessions completed).
Conditions Studied
Interventions
- BEHAVIORAL Meditation
Study Locations (1)
Massachusetts
- Beth Israel Deaconess Medical Center - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 29 participants |
| Start Date | 2017-11-28 |
| Est. Completion | 2020-04-30 |
| Phase | NA |
What the finished NCT03198039 record still lists
NCT03198039 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 29 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (98% lower).
The record links to 1 condition, with Feasibility of a Meditation Program Perioperatively appearing as the primary indexed condition, and to 1 intervention - of which Meditation is the first listed.
NCT03198039 reports a single indexed study location in Massachusetts.
Frequently Asked Questions
What is clinical trial NCT03198039 about?
NCT03198039 is a clinical study titled "Guided Meditation as an Adjunct to Enhance Postoperative Recovery". The primary purpose of this trial is to test the feasibility of implementing a meditation program in the perioperative period.
What is the current status of trial NCT03198039?
This trial is currently completed. It is a NA study. The enrollment target is 29 participants. The study started on 2017-11-28. Estimated completion is 2020-04-30.
What conditions does trial NCT03198039 study?
This clinical trial studies the following conditions: Feasibility of a Meditation Program Perioperatively.
What interventions are being tested in trial NCT03198039?
The interventions under investigation include: Meditation (BEHAVIORAL).
Who is sponsoring clinical trial NCT03198039?
This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03198039 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03198039's enrollment target sits among peer trials
29 1702nd of 2000 higher than 297 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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