MedPath

The Effect of Compassion-Focused Therapy (CFT) in Patients with Vitiligo

Not Applicable
Recruiting
Conditions
Vitiligo.
Vitiligo
Registration Number
IRCT20201103049252N1
Lead Sponsor
Shahid Beheshti University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
40
Inclusion Criteria

1. Diagnosis of the disease based on clinical evidence such as the appearance of skin lesions and, if necessary, by skin sampling and confirmation of vitiligo by a dermatologist 2. Age range 20 to 45 years 3. Having at least primary education 4. At least six months of disease history 5. Completing the informed consent form based on voluntary participation in the study and not receiving psychological services outside the treatment session

Exclusion Criteria

1. Have diagnostic criteria for obvious psychiatric disorders based on clinical interview 2. Addiction or alcohol consumption 3. History of being hospitalized in psychiatric wards 4. Consumption of psychiatric drugs 5. Participate in treatment programs related to compassion-focused treatment during the past six months

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Self-critical. Timepoint: The variable is measured before performing the protocol. After performing the protocol, the variable is measured and then measured again three weeks later. Method of measurement: Thomson and Zarov self-critical levels scale.;Internalized shame. Timepoint: The variable is measured before performing the protocol. After performing the protocol, the variable is measured and then measured again three weeks later. Method of measurement: Internalized Shame Scale.;Resilience. Timepoint: The variable is measured before performing the protocol. After performing the protocol, the variable is measured and then measured again three weeks later. Method of measurement: Connor & Davidson Resilience Scale.;Quality of Life. Timepoint: The variable is measured before performing the protocol. After performing the protocol, the variable is measured and then measured again three weeks later. Method of measurement: World Health Organization Quality of Life Questionnaire.
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath