Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04855968 · ClinicalTrials.gov registry record · NA

The Effect of Mindfulness/Meditation on Post-operative Pain and Opioid Consumption

A NA study, sponsored by Cedars-Sinai Medical Center.

Terminated
Registry status
NA
Development phase
55
Enrollment target

NCT04855968: Clinical Trial NA study, sponsored by Cedars-Sinai Medical Center.

NCT04855968 is a NA study that was terminated before completion, run by Cedars-Sinai Medical Center. The registered enrollment target is 55 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04855968, a NA study, was terminated before completion, sponsored by Cedars-Sinai Medical Center.

TERMINATED
Registry status
NA
Development phase
55 participants
Enrollment target

Study Summary

The objective of this study is to examine the effectiveness of mindfulness/meditation using the Headspace App on post-operative pain and opioid consumption in patients after arthroscopic rotator cuff repairs, biceps tenodesis, and Mumford procedures.

Primary Outcome

single-item measure of pain and consists of a 100 millimeter (mm) horizontal line with the labels "No Pain" at the leftmost portion and "Worst Pain" at the rightmost portion of the line

Interventions

  • OTHER In addition to standard post-op medication patient will have access to the head space meditation application.
  • OTHER Patients will take standard post-op pain medication

Trial Details

FieldValue
Enrollment Target 55 participants
Start Date 2020-09-01
Est. Completion 2021-09-01
Phase NA
Cedars-Sinai Medical Center

339 total trials

Why NCT04855968 stopped before completion

NCT04855968 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 55 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which In addition to standard post-op medication patient will have access to the head space meditation application. is the first listed.

NCT04855968 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04855968 about?

NCT04855968 is a clinical study titled "The Effect of Mindfulness/Meditation on Post-operative Pain and Opioid Consumption". The objective of this study is to examine the effectiveness of mindfulness/meditation using the Headspace App on post-operative pain and opioid consumption in patients after arthroscopic rotator cuff repairs, biceps tenodesis, and Mumford procedures.

What is the current status of trial NCT04855968?

This trial is currently terminated. It is a NA study. The enrollment target is 55 participants. The study started on 2020-09-01. Estimated completion is 2021-09-01.

What interventions are being tested in trial NCT04855968?

The interventions under investigation include: In addition to standard post-op medication patient will have access to the head space meditation application. (OTHER), Patients will take standard post-op pain medication (OTHER).

Who is sponsoring clinical trial NCT04855968?

This trial is sponsored by Cedars-Sinai Medical Center, which has 339 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04855968's enrollment target sits among peer trials

55 1264th of 2000 higher than 733 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT01638676 · 55 participants · Phase 1

    A Phase I/II Trial of Vemurafenib and Metformin to Melanoma Patients

  • NCT01906385 · 55 participants · Phase 1

    Maximum Tolerated Dose, Safety, and Efficacy of Rhenium Nanoliposomes in Recurrent Glioma (ReSPECT)

  • NCT03007030 · 55 participants · Phase 2

    Brentuximab Vedotin in Treating Patients With CD30+ Malignant Mesothelioma That Cannot Be Removed by Surgery

  • NCT03152058 · 55 participants · Phase 2

    IMPACT Study: IMProve Pregnancy in APS With Certolizumab Therapy

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04855968, the US trial registry maintained by the National Library of Medicine. NCT04855968 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.