Supporting Evidence-based Responses to Emotional Needs in Emphysema

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to understand how a Coping Skills Training program can reduce depression and anxiety in people with chronic obstructive pulmonary disease (COPD), particularly those who face health disparities, including those with low income, different racial backgrounds, or those living in rural areas. The main questions it aims to answer are: * How does the Coping Skills Training program help reduce stress and anxiety in patients? * What causes variations in the effectiveness of the Coping Skills Training program? * What are the barriers and facilitators to the uptake of the Coping Skills Training program? Researchers will compare a 12-week Coping Skills Training program with a COPD Education program to see if the training leads to better health outcomes for participants. Participants will: * Take part in weekly 30-minute sessions for 12 weeks if assigned to the Coping Skills Training group. * Take part in weekly 10-minute sessions for 12 weeks if assigned to the COPD Education group. * Complete surveys before, during, and after the intervention. * Patients and caregivers, including those who chose not to enroll, as well as clinicians, will be invited to participate in interviews to share their perspectives.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

⁃ Patients

• Be at least 18 years of age

• Have a documented diagnosis of COPD and confirmation of obstructive lung disease by spirometry (American Thoracic Society/European Respiratory Society guidelines) or radiology (imaging report indicating emphysematous changes)

• Score greater than or equal to 8 during baseline screening using the PHQ-8

• Identify an adult caregiver to participate with them

• Have the ability to access a telephone or videoconferencing call up to once weekly (for approximately 30 minutes) for 12 sessions of the study intervention

• Spoken proficiency in Spanish and/or English

⁃ Caregivers

• Be at least 18 years of age

• Have the ability to access a telephone or videoconferencing call up to once weekly (for approximately 30 minutes) for 12 weeks

Locations
United States
Michigan
Henry Ford Health System
NOT_YET_RECRUITING
Detroit
Pennsylvania
University of Pennsylvania
RECRUITING
Philadelphia
Contact Information
Primary
Joanna Hart, MD, MSHP
Joanna.Hart@pennmedicine.upenn.edu
267-271-0665
Backup
Daniel Carter, PhD
Daniel.Carter@pennmedicine.upenn.edu
215-573-7082
Time Frame
Start Date: 2024-09-30
Estimated Completion Date: 2028-03-05
Participants
Target number of participants: 750
Treatments
Experimental: Coping Skills Training
Experimental: COPD Education
Sponsors
Collaborators: National Institute of Nursing Research (NINR), Thomas Jefferson University, Henry Ford Health System
Leads: University of Pennsylvania

This content was sourced from clinicaltrials.gov

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