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The effectiveness of Cognitive Behavior Therapy with Narrow-band Ultraviolet B Phototherapy to relieve psoriasis

The effectiveness of Cognitive Behavior Therapy with Narrow-band Ultraviolet B Phototherapy to relieve psoriasis

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20241005003
Enrollment
60
Registered
2024-10-05
Start date
2024-10-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psoriasis Psoriasis, Phototherapy, Cognitive Behavior Therapy, Disease Severity, Quality of Life, Depression

Interventions

Cognitive behavioral therapy is a group activity in which patients receive therapy from a cognitive behavioral therapist once a week for 1 hour and 30 minutes each time for a total of 8 weeks. They ar
feelings of anxiety and sadness. - Week 3: Relax, feel comfortable, and relax, is to let members learn and practice relaxation skills and share ways to manage stress with each other. - Week 4: Is thin
Psoriasis patients receiving cognitive behavioral therapy (CBT) in combination with Narrow-band Ultraviolet B Phototherapy (NB-UVB),Psoriasis patients receiving standard Narrow-band Ultraviolet B Phot

Sponsors

Institute of Dermatology
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 years and over, both male and female, who have been diagnosed by a doctor with Psoriasis. 2. Have moderate to severe psoriasis (PASI score greater than or equal to 5) 3. Have received narrowband UVB (NB-UVB) radiation 4. Have a tendency to be depressed, with 1 of 2 symptoms, as assessed by the 2-question depression screening form (2Q) 5. Have no problems with hearing, vision, or speech 6. Have full consciousness, can read and write Thai 7. Consent to participate in the study willingly

Exclusion criteria

Exclusion criteria: 1. Patients receiving Biologic drugs 2. Have a history of psychiatric disorders within the past 2 years, such as generalized anxiety disorder, depression, psychosis, schizophrenia, bipolar disorder 3. Are undergoing treatment or receiving antidepressant medication or other psychotropic drugs or receiving other forms of psychotherapy

Design outcomes

Primary

MeasureTime frame
Psoriasis Area and Severity Index Five assessments were performed: before the trial (T0), after the trial (T1), one month after the trial (T2), three months after the trial (T3), and six months after the trial (T4). The PASI score was assessed by a physician

Secondary

MeasureTime frame
Anxiety and Depression Five assessments were performed: before the trial (T0), after the trial (T1), one month after the trial (T2), three months after the trial (T3), and six months after the trial (T4). questionnaire Thai Hospital Anxiety and Depression Scale (Thai HADS ),Psoriasis Symptom Three assessments were performed: before the trial (T0), after the trial (T1), and six months after the trial (T4). questionnaire PSS,Dermatology Life Quality Index Five assessments were performed: before the trial (T0), after the trial (T1), one month after the trial (T2), three months after the trial (T3), and six months after the trial (T4). questionnaire DLQI,Quality of Life Three assessments were performed: before the trial (T0), after the trial (T1), and six months after the trial (T4). questionnaire EQ-5D-5L

Countries

Thailand

Contacts

Public ContactSirintip Thongkaow

Chulalongkorn University

micky_sirintip@live.com023545222

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026