MedPath

Psychological Treatments for Scleroderma

Phase 2
Completed
Conditions
Depression
Systemic Sclerosis
Pain
Scleroderma
Interventions
Behavioral: Self-help cognitive behavioral intervention facilitated by a psychologist
Behavioral: Cognitive behavioral therapy
Behavioral: Disease/health education
Registration Number
NCT00007267
Lead Sponsor
Johns Hopkins University
Brief Summary

This study will examine the effectiveness of two psychological treatment approaches designed to help people who have scleroderma with three important areas of daily living: pain, depression, and distress about changes in appearance. The study will also evaluate the impact of depression on the two psychological treatments. Because psychological approaches requiring a trained professional can be expensive and are often not available to most patients, this study will also look at the effectiveness of a self-help treatment approach.

Detailed Description

This study will examine the efficacy of psychological interventions designed to target important areas of daily living for people with scleroderma: pain, depression, and distress about disfigurement. The study will also examine the effect of clinical depression on impact of the psychological treatments. Because psychological interventions requiring a trained professional can be costly and are often not available to the majority of patients, the study will also examine the efficacy of a self-help intervention.

The study will recruit 201 patients with systemic sclerosis who report symptoms of pain, depression, or distress about disfigurement and will randomly assign them to one of three interventions: individual cognitive behavioral therapy, self-help cognitive behavioral intervention facilitated by a psychologist, or a disease/health education intervention. An individual blinded to intervention assignment will collect measures of pain, functioning, distress about disfigurement, and mood at baseline and following the 8-week intervention period.

Both the cognitive-behavioral self-help materials and the educational materials (eight written chapters and audiotapes) will be designed for home use but will be supplemented by two individual sessions and two telephone contacts with the professional. Patients will be followed for 1 year after completing the active intervention phase.

These findings will increase understanding of the quality of life of individuals with scleroderma and determine whether self-help interventions can be used effectively to manage pain, depression, and distress about disfigurement.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
89
Inclusion Criteria
  • Diagnosis of CREST or systemic sclerosis
  • Short-Form McGill Pain Questionnaire score 6 or higher
  • Satisfaction with Appearance score of 15 or higher
  • Beck Depression score of 10 or higher
Exclusion Criteria
  • Patients reporting severe depression with suicidal ideation
  • Delirium, dementia, or cognitive impairment (Mini Mental State Examination (MMSE) < 24))
  • Terminal illness with a life expectancy of less than 1 year

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
2Self-help cognitive behavioral intervention facilitated by a psychologistParticipants will receive self-help cognitive behavioral intervention facilitated by a psychologist
1Cognitive behavioral therapyParticipants will receive individual cognitive behavioral therapy
3Disease/health educationParticipants will receive a disease/health education intervention
Primary Outcome Measures
NameTimeMethod
Depressive symptomsMeasured at Week 8
Secondary Outcome Measures
NameTimeMethod
Body image dissatisfactionMeasured at Week 8
PainMeasured at Week 8

Trial Locations

Locations (1)

Johns Hopkins Bayview Medical Center

🇺🇸

Baltimore, Maryland, United States

© Copyright 2025. All Rights Reserved by MedPath