Collaborative Care Intervention for Chronic Kidney Disease
- Conditions
- Kidney TransplantDepressionPain
- Interventions
- Behavioral: Collaborative care
- Registration Number
- NCT02938351
- Lead Sponsor
- University of Pittsburgh
- Brief Summary
The aims of the present study will be to pilot test the efficacy of a collaborative care intervention in patients awaiting kidney transplant to reduce symptoms of depression, pain, fatigue and improve quality of life.
- Detailed Description
Symptom management is critical to maintain quality of life in those with life limiting conditions. Stepped collaborative care interventions have been widely employed in the primary care setting for the treatment of depression and more recently have been utilized to treat other symptoms (e.g., pain) in a variety of settings. A recent meta-analyses concluded that collaborative care interventions were superior to usual care and are more cost-effective than face to face and pharmacological treatment for depression. Collaborative care interventions have begun to be extended to other settings but have not been tested in patients who are being treated with dialysis. The aims of the present study were to pilot test the efficacy of a collaborative care intervention in patients awaiting kidney transplant to reduce symptoms of depression, pain, fatigue and improve quality of life.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 10
Age 18 or older Currently receiving dialysis at UPMC dialysis facility for chronic kidney disease Fluent in English
Under the age of 18 years or over 90 years Not fluent in English
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description collaborative care Collaborative care To test the efficacy of a collaborative care intervention with patients treated with dialysis to reduce depression, pain, fatigue, and improve quality of life
- Primary Outcome Measures
Name Time Method degree of Pain change from baseline at 3 month and 6 month score on the BPI questionnaire
Perceived Stress level change from baseline at 3 month and 6 month score on PSS questionnaire
Depression Level change from baseline at 3 month and 6 month score on CES-D questionnaire
- Secondary Outcome Measures
Name Time Method Dyadic functioning change from baseline at 3 month and 6 month score on the Dyadic functioning questionnaire
level of physical activity (mild, moderate or high) change from baseline at 3 month and 6 month calculated score on the International Physical Activity quationnaire
sleep quality change from baseline at 3 month and 6 month score on the PSQI questionnaire
quality of life change from baseline at 3 month and 6 month score on the KDQOL questionnaire
Trial Locations
- Locations (1)
University of Pittsburgh Medical Center
🇺🇸Pittsburgh, Pennsylvania, United States