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creating and verifying intake form for adults with skin disorders and related psychological issues

Development and Validation of Psychodermatology Proforma for Adults - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/05/068188
Enrollment
15
Registered
2024-05-31
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-24

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

Conditions

Health Condition 1: L00-L99- Diseases of the skin and subcutaneous tissue Health Condition 2: F01-F99- Mental, Behavioral and Neurodevelopmental disorders

Interventions

Control Intervention1: NA: NA

Sponsors

Sonam S Mathew
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Phase I: Selection of expert panel In the first phase of the study, validation of the proforma will be done by experts fulfilling the following criteria. Inclusion criteria for Phase I Consultants from department of dermatology, clinical psychology, and psychiatry. Consultants must be actively part of the Psychodermatology Liaison Clinic. Minimum of three years of experience as a consultant in Psychodermatology liaison clinic. Phase II: recruitment of participants for Pilot study Individuals 18 years and above Belonging to any Gender Diagnosed with at least one psychodermatological condition. Can converse and comprehend in English, Kannada, Malayalam or Tamil.

Exclusion criteria

Exclusion criteria: nil

Design outcomes

Primary

MeasureTime frame
Phase I Outcome measures 1. Main domains for proforma- measured by Content Validity Index, scores ranging between 0 to 1. 2. Subdomains for proforma- measured by Content Validity Index, scores ranging between 0 to 1. 3. Placement of Domains in the Proforma- measured by Content Validity Index, scores ranging between 0 to 1. 4. Flow of the proforma- measured by Content Validity index, scores ranging between 0 to 1.Timepoint: baseline—

Secondary

MeasureTime frame
Phase II Outcome measures 1.Duration- measures average time taken to administer the proforma, measured in minutes. 2. Flow of the proforma- measured by agreement rate on likert scale between 1 to 5. 3. Clarity-measured by agreement rate on likert scale between 1 to 5. 4.Comprehensiveness- measured by agreement rate on likert scale between 1 to 5. 5.Relevance- measured by agreement rate on likert scale between 1 to 5.Timepoint: baseline—

Countries

India

Contacts

Public ContactMs Anagha S Deshmukh

Manipal College of Health Professions

v.anupama@manipal.edu9739016983

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026