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NCT06180486 · ClinicalTrials.gov registry record · NA
Mindfulness Meditation Intervention Study
A NA study of Total Knee Replacement and Feasibility, sponsored by Hospital for Special Surgery, New York.
- Completed
- Registry status
- NA
- Development phase
- 30
- Enrollment target
- 1
- Study location
NCT06180486: Completed NA study of Total Knee Replacement and Feasibility, sponsored by Hospital for Special Surgery, New York.
NCT06180486 is a NA study of Total Knee Replacement and Feasibility that has completed, run by Hospital for Special Surgery, New York. The registered enrollment target is 30 participants, below the 212-participant average among 9 other Total Knee Replacement trials with a reported enrollment target (86% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06180486, a NA study of Total Knee Replacement and Feasibility, has completed, sponsored by Hospital for Special Surgery, New York.
- COMPLETED
- Registry status
- NA
- Development phase
- 30 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this pilot study is to develop a randomized control trial study with sufficient power to definitely address if a preop mindfulness meditation intervention can improve post-total knee arthroplasty mental well-being or physical health compared to controls, and if a preop mindfulness meditation intervention can train resilience. The main questions it aims to answer are: 1. Is this preoperative mindfulness meditation study feasible at Hospital for Special Surgery? 2. Can we estimate a control and intervention group central tendency and variability to be used to determine sample size in future study? 3. Does a preoperative mindfulness meditation interventions improve post-total knee arthroplasty mental well-being or physical health compared to controls? Can preoperative a mindfulness meditation intervention train resilience (as measured by increased resilience score)? Participants will be randomly assigned to be in the intervention group or the waitlist control group. The intervention group gets the mindfulness mediation intervention prior to their day of surgery, and the control group will be given the mindfulness meditation intervention 90 days after their day of surgery. The waitlist control group allows for comparison between those who got the mindfulness meditation intervention prior to surgery and those who did not while still offering the potential benefits of the intervention after 90 days.
Primary Outcome
PROMIS Mental Health Questionnaire is to assess general mental health in patients 1 week prior to surgery, post operative day 14, and post operative day 90. The responses to these questionsare excellent, very good, good, fair, or poor.
Conditions Studied
Interventions
- OTHER Mindfulness Meditation Intervention
Study Locations (1)
New York
- Hospital for Special Surgery - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 30 participants |
| Start Date | 2024-02-02 |
| Est. Completion | 2025-02-11 |
| Phase | NA |
What the finished NCT06180486 record still lists
NCT06180486 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 212-participant average among 9 other Total Knee Replacement trials with a reported enrollment target (86% lower).
The record links to 3 conditions, with Total Knee Replacement appearing as the primary indexed condition, and to 1 intervention - of which Mindfulness Meditation Intervention is the first listed.
NCT06180486 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT06180486 about?
NCT06180486 is a clinical study titled "Mindfulness Meditation Intervention Study". The goal of this pilot study is to develop a randomized control trial study with sufficient power to definitely address if a preop mindfulness meditation intervention can improve post-total knee arthroplasty mental well-being or physical health compared to controls, and if a preop mindfulness medita...
What is the current status of trial NCT06180486?
This trial is currently completed. It is a NA study. The enrollment target is 30 participants. The study started on 2024-02-02. Estimated completion is 2025-02-11.
What conditions does trial NCT06180486 study?
This clinical trial studies the following conditions: Total Knee Replacement, Feasibility, Mediation.
What interventions are being tested in trial NCT06180486?
The interventions under investigation include: Mindfulness Meditation Intervention (OTHER).
Who is sponsoring clinical trial NCT06180486?
This trial is sponsored by Hospital for Special Surgery, New York, which has 194 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06180486 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Where NCT06180486's enrollment target sits among peer trials
30 9th of 9 higher than 1 of 9 other Total Knee Replacement trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Total Knee Replacement 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.
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