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NCT06831838 · ClinicalTrials.gov registry record · NA
A Randomized Controlled Trial (RCT) to Determine the Efficacy of a Multidisciplinary CBT Based Pain Management Program for the Treatment of Aromatase Inhibitor Associated Musculoskeletal Symptoms (AIMSS) in Breast Cancer Survivors
A NA study of Breast Cancer, sponsored by Mayo Clinic.
- Recruiting
- Registry status
- NA
- Development phase
- 115
- Enrollment target
- 1
- Study location
NCT06831838 is a NA study of Breast Cancer that is actively recruiting participants, run by Mayo Clinic. The registered enrollment target is 115 participants, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (96% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06831838, a NA study of Breast Cancer, is actively recruiting participants, sponsored by Mayo Clinic.
- RECRUITING
- Registry status
- NA
- Development phase
- 115 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this research is to evaluate the effectiveness of a multidisciplinary pain management program for AIMSS in reducing pain, subjective cognitive complaints, psychological distress, and impaired functional status resulting in improved adherence to Aromatase Inhibitor medications compared to usual care. We want to identify predictors of improvement in pain, functional status, subjective cognition and mood following participation in the program.
Conditions Studied
Interventions
- BEHAVIORAL Cognitive Behavioral Therapy based Pain Management Program
Study Locations (1)
Florida
- Mayo Clinic in Florida - Jacksonville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 115 participants |
| Start Date | 2025-02-06 |
| Est. Completion | 2026-12 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06831838
The ClinicalTrials.gov registry entry for NCT06831838 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 115 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (96% lower). The listed sponsor is Mayo Clinic, which has 2,844 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Breast Cancer appearing as the primary indexed condition, and to 1 intervention - of which Cognitive Behavioral Therapy based Pain Management Program is the first listed.
NCT06831838 reports 1 study location spanning 1 distinct geographic area - top geographies include Florida.
Frequently Asked Questions
What is clinical trial NCT06831838 about?
NCT06831838 is a clinical study titled "A Randomized Controlled Trial (RCT) to Determine the Efficacy of a Multidisciplinary CBT Based Pain Management Program for the Treatment of Aromatase Inhibitor Associated Musculoskeletal Symptoms (AIMSS) in Breast Cancer Survivors". The purpose of this research is to evaluate the effectiveness of a multidisciplinary pain management program for AIMSS in reducing pain, subjective cognitive complaints, psychological distress, and impaired functional status resulting in improved adherence to Aromatase Inhibitor medications compared...
What is the current status of trial NCT06831838?
This trial is currently recruiting. It is a NA study. The enrollment target is 115 participants. The study started on 2025-02-06. Estimated completion is 2026-12.
What conditions does trial NCT06831838 study?
This clinical trial studies the following conditions: Breast Cancer.
What interventions are being tested in trial NCT06831838?
The interventions under investigation include: Cognitive Behavioral Therapy based Pain Management Program (BEHAVIORAL).
Who is sponsoring clinical trial NCT06831838?
This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06831838 being conducted?
This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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