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NCT06976138 · ClinicalTrials.gov registry record · NA

Sleep TO Prevent Post-surgical Pain

A NA study of Knee Osteoarthristis, sponsored by Johns Hopkins University.

Recruiting
Registry status
NA
Development phase
252
Enrollment target
2
Study locations

NCT06976138: Recruiting NA study of Knee Osteoarthristis, sponsored by Johns Hopkins University.

NCT06976138 is a NA study of Knee Osteoarthristis that is actively recruiting participants, run by Johns Hopkins University. The registered enrollment target is 252 participants, below the 430-participant average among 3 other Knee Osteoarthristis trials with a reported enrollment target (41% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06976138, a NA study of Knee Osteoarthristis, is actively recruiting participants, sponsored by Johns Hopkins University.

RECRUITING
Registry status
NA
Development phase
252 participants
Enrollment target
2
Study locations

Study Summary

This research study is being done to compare different methods of addressing sleep problems before total knee replacement surgery. These methods include Cognitive Behavioral Therapy and light exposure.

Primary Outcome

Higher scores indicate higher pain. Asked to rate pain in different situations from 0 (no pain) to 10 (extreme pain) on Visual Analog Scale.

Conditions Studied

Interventions

  • BEHAVIORAL Cognitive-Behavioral Therapy for Insomnia
  • DEVICE Bright Light therapy via the Re-Timer®
  • DEVICE Negative Ion exposure via IonMi Device
  • BEHAVIORAL Sleep / Knee Osteoarthritis Education

Study Locations (2)

Maryland

  • Johns Hopkins School of Medicine - Baltimore

Massachusetts

  • Mass General Brigham - Chestnut Hill

Trial Details

FieldValue
Enrollment Target 252 participants
Start Date 2025-06-13
Est. Completion 2029-07-31
Phase NA
Johns Hopkins University

1,448 total trials

What NCT06976138 shows while recruiting

NCT06976138 is an interventional study that assigns participants to a tested intervention. The registered 252 participants enrollment target is mid-sized for trials with a published cap, below the 430-participant average among 3 other Knee Osteoarthristis trials with a reported enrollment target (41% lower).

The record links to 1 condition, with Knee Osteoarthristis appearing as the primary indexed condition, and to 4 interventions - of which Cognitive-Behavioral Therapy for Insomnia is the first listed.

NCT06976138 reports a single indexed study location in Maryland, Massachusetts.

Frequently Asked Questions

What is clinical trial NCT06976138 about?

NCT06976138 is a clinical study titled "Sleep TO Prevent Post-surgical Pain". This research study is being done to compare different methods of addressing sleep problems before total knee replacement surgery. These methods include Cognitive Behavioral Therapy and light exposure.

What is the current status of trial NCT06976138?

This trial is currently recruiting. It is a NA study. The enrollment target is 252 participants. The study started on 2025-06-13. Estimated completion is 2029-07-31.

What conditions does trial NCT06976138 study?

This clinical trial studies the following conditions: Knee Osteoarthristis.

What interventions are being tested in trial NCT06976138?

The interventions under investigation include: Cognitive-Behavioral Therapy for Insomnia (BEHAVIORAL), Bright Light therapy via the Re-Timer® (DEVICE), Negative Ion exposure via IonMi Device (DEVICE), Sleep / Knee Osteoarthritis Education (BEHAVIORAL).

Who is sponsoring clinical trial NCT06976138?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06976138 being conducted?

This trial has 2 study locations across Maryland, Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT06976138, the US trial registry maintained by the National Library of Medicine. NCT06976138 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.