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Recruiting NCT06831838

NCT06831838 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

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Clinical Trial Summary
NCT ID NCT06831838
Status Recruiting
Phase
Sponsor Mayo Clinic
Condition Breast Cancer
Study Type INTERVENTIONAL
Enrollment 115 participants
Start Date 2025-02-06
Primary Completion 2026-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Cognitive Behavioral Therapy based Pain Management Program

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 115 participants in total. It began in 2025-02-06 with a primary completion date of 2026-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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.

Eligibility Criteria

Inclusion Criteria: * At least 18 years old * ECOG ≤ 2 * Stage 0-III HR+ breast cancer in need of strategies to reduce symptoms and improve quality of life Exclusion Criteria: • Less than 18 years of age. \- Stage 4 HR+ breast cancer

Contact & Investigator

Central Contact

Alejandra Cuartas-Abril, M.S.

✉ Cuartas-Abril.Alejandra@mayo.edu

📞 904-956-8885

Principal Investigator

Barbara Bruce, Ph.D., LP

PRINCIPAL INVESTIGATOR

Mayo Clinic

Frequently Asked Questions

Who can join the NCT06831838 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Breast Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06831838 currently recruiting?

Yes, NCT06831838 is actively recruiting participants. Contact the research team at Cuartas-Abril.Alejandra@mayo.edu for enrollment information.

Where is the NCT06831838 trial being conducted?

This trial is being conducted at Jacksonville, United States.

Who is sponsoring the NCT06831838 clinical trial?

NCT06831838 is sponsored by Mayo Clinic. The principal investigator is Barbara Bruce, Ph.D., LP at Mayo Clinic. The trial plans to enroll 115 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology