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

NCT06952049 · ClinicalTrials.gov registry record · NA

Does Psychoeducation Improve the Pain Relief Derived From a Brief Intervention

A NA study, sponsored by Florida State University.

Completed
Registry status
NA
Development phase
646
Enrollment target

NCT06952049: Completed NA study, sponsored by Florida State University.

NCT06952049 is a NA study that has completed, run by Florida State University. The registered enrollment target is 646 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (54% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06952049, a NA study, has completed, sponsored by Florida State University.

COMPLETED
Registry status
NA
Development phase
646 participants
Enrollment target

Study Summary

This project is a single-site, five-arm, randomized controlled trial investigating whether providing patients in an orthopedic clinic waiting room psychoeducation about mindfulness impacts the degree of pain relief they experience during a mindfulness-based intervention.

Primary Outcome

Change in acute pain unpleasantness will be measured with an individual item ("How unpleasant is your pain, right now?") rated on a numeric rating scale. Scores range from 0 to 10, with higher scores reflecting greater acute pain unpleasantness.

Interventions

  • BEHAVIORAL Pain Psychoeducation
  • BEHAVIORAL Mindfulness without Psychoeducation
  • BEHAVIORAL 1 Minute Psychoeducation with 2 Minutes of Mindfulness (Pain Focus)
  • BEHAVIORAL 1 Minute Psychoeducation with 2 Minutes of Mindfulness (Meaning Focus)
  • BEHAVIORAL 2 Minutes of Psychoeducation with 1 Minute of Mindfulness

Trial Details

FieldValue
Enrollment Target 646 participants
Start Date 2025-04-10
Est. Completion 2025-12-18
Phase NA
Florida State University

219 total trials

What the finished NCT06952049 record still lists

NCT06952049 is an interventional study that assigns participants to a tested intervention. The registered 646 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 (54% lower).

The record links to 0 conditions, and to 5 interventions - of which Pain Psychoeducation is the first listed.

NCT06952049 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06952049 about?

NCT06952049 is a clinical study titled "Does Psychoeducation Improve the Pain Relief Derived From a Brief Intervention". This project is a single-site, five-arm, randomized controlled trial investigating whether providing patients in an orthopedic clinic waiting room psychoeducation about mindfulness impacts the degree of pain relief they experience during a mindfulness-based intervention.

What is the current status of trial NCT06952049?

This trial is currently completed. It is a NA study. The enrollment target is 646 participants. The study started on 2025-04-10. Estimated completion is 2025-12-18.

What interventions are being tested in trial NCT06952049?

The interventions under investigation include: Pain Psychoeducation (BEHAVIORAL), Mindfulness without Psychoeducation (BEHAVIORAL), 1 Minute Psychoeducation with 2 Minutes of Mindfulness (Pain Focus) (BEHAVIORAL), 1 Minute Psychoeducation with 2 Minutes of Mindfulness (Meaning Focus) (BEHAVIORAL), 2 Minutes of Psychoeducation with 1 Minute of Mindfulness (BEHAVIORAL).

Who is sponsoring clinical trial NCT06952049?

This trial is sponsored by Florida State University, which has 219 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06952049's enrollment target sits among peer trials

646 156th of 2000 higher than 1,845 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

  • NCT04863222 · 646 participants · Phase 4

    Clinical and Radiographic Success of MTA vs Biodentine

  • NCT07012395 · 645 participants · Phase 2

    A Study of Long-acting Antibodies Alone and in Combinations for Moderate to Severe Ulcerative Colitis

  • NCT07027306 · 648 participants

    The Osteoporotic Fracture Classification-based Scoring System for Treatment Decision in Thoracolumbar Osteoporotic Fractures

  • NCT07164456 · 648 participants · NA

    Together Stronger: A Family-centered Lifestyle Intervention for Black Prostate Cancer Survivors and Their Caregivers

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 NCT06952049, the US trial registry maintained by the National Library of Medicine. NCT06952049 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.