MedPath

Collaborative Care Intervention for Chronic Kidney Disease

Not Applicable
Completed
Conditions
Kidney Transplant
Depression
Pain
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
Inclusion Criteria

Age 18 or older Currently receiving dialysis at UPMC dialysis facility for chronic kidney disease Fluent in English

Exclusion Criteria

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
GroupInterventionDescription
collaborative careCollaborative careTo 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
NameTimeMethod
degree of Painchange from baseline at 3 month and 6 month

score on the BPI questionnaire

Perceived Stress levelchange from baseline at 3 month and 6 month

score on PSS questionnaire

Depression Levelchange from baseline at 3 month and 6 month

score on CES-D questionnaire

Secondary Outcome Measures
NameTimeMethod
Dyadic functioningchange 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 qualitychange from baseline at 3 month and 6 month

score on the PSQI questionnaire

quality of lifechange 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

© Copyright 2025. All Rights Reserved by MedPath