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Brief Pain Coping Skills Training for Older Women With Breast Cancer and Pain: An Efficacy-Effectiveness Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This randomized controlled trial examines a 1-session, telehealth pain coping skills training (PCST) protocol with five 15-minute maintenance calls (Brief PCST-Community) adapted for women with breast cancer in medically underserved areas. Pain, health-related quality of life, and self-efficacy for pain management will be assessed at baseline and 10 and 15 weeks later.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 55
Healthy Volunteers: f
View:

• Receiving cancer care at a Duke Cancer Network (DCN) clinic

• Stage I-IV breast cancer

• Self-reported pain on at least 10 days in the last month and pain rating of worst pain of 4 or greater on a 0-10 scale in the last week

• Biologically female

• Greater than or equal to 55 years old

• Ability to speak and read English

• Hearing and vision that allows for successful completion of videoconferencing and phone session

Locations
United States
North Carolina
Duke Cancer Network
RECRUITING
Durham
Contact Information
Primary
Tamara Somers, PhD
tamara.somers@duke.edu
919-416-3408
Time Frame
Start Date: 2026-06-30
Estimated Completion Date: 2027-06-01
Participants
Target number of participants: 168
Treatments
Experimental: Pain Coping Skills Training
Participants in this group will complete a 50-minute telehealth session with a trained study nurse. During this session, they will be taught how to use several coping strategies for managing pain. This will be followed by 5 weekly, 15-minute supportive phone calls, where the study nurse will reinforce the learned coping skills. They will be asked to complete 2 follow-up surveys (10 weeks and 15 weeks after the first survey).
No_intervention: Usual Care
Participants in this group will not complete the new program. They will be asked to complete 2 follow-up surveys (10 and 15 weeks after the first survey).
Related Therapeutic Areas
Sponsors
Leads: Duke University
Collaborators: National Institute on Aging (NIA)

This content was sourced from clinicaltrials.gov