- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07711574
Prevalence of Depression Among Patients With Alopecia Areata (AA_DEP)
Assessment of the Prevalence and Severity of Depression Among Patients With Alopecia Areata Attending Dermatology Clinics: A Cross-Sectional Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This is a cross-sectional observational study designed to evaluate the prevalence of depression among patients with alopecia areata attending the dermatology outpatient clinic at Sohag University Hospital. Alopecia areata is an autoimmune condition characterized by non-scarring hair loss and may be associated with psychological distress.
The study will include patients diagnosed clinically with alopecia areata. Data will be collected through structured interviews and the use of a validated depression screening questionnaire. No therapeutic intervention will be applied during the study.
The aim of the study is to assess the psychological burden of alopecia areata and identify the frequency of depressive symptoms among affected patients. The findings may help in improving holistic patient care by addressing both dermatological and psychological aspects of the disease.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Omima Atef, MD
- Phone Number: 01098970741
- Email: omimaatef64@gmail.com
Study Locations
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-
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Sohag, Egypt
- Sohag university hospital
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Contact:
- Omima Atef, MD
- Phone Number: 01098970741
- Email: omimaatef64@gmail.com
-
Contact:
- Email: omimaatef64@gmail.com
-
Principal Investigator:
- Omima Atef, MD
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patients diagnosed with alopecia areata Age 18 years and above Attending dermatology outpatient clinic at Sohag University Hospital Willing to participate and provide informed consent
Exclusion Criteria:
- Patients with other causes of hair loss Patients with known psychiatric disorders prior to alopecia areata diagnosis Patients refusing participation
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Alopecia areata patients
Patients diagnosed with alopecia areata attending the dermatology outpatient clinic at Sohag University Hospital.
This is an observational cross-sectional study with no interventions.
Data will be collected using a structured questionnaire to assess depressive symptoms.
|
This is an observational cross-sectional study with no therapeutic or experimental intervention.
Data will be collected using a structured questionnaire to assess depression among patients with alopecia areata.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Prevalence of depression among patients with alopecia areata
Time Frame: At enrollment
|
The primary outcome is to assess the prevalence of depressive symptoms among patients with alopecia areata attending the dermatology outpatient clinic at Sohag University Hospital.
Depression will be evaluated using a structured validated questionnaire.
|
At enrollment
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Omima Atef, MD, ? Faculty of Medicine, Sohag University, Egypt
- Principal Investigator: Omima Atef, ? Faculty of Medicine, Sohag University, Egypt
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- AA _ Dep_ Omima _ sohag _2026
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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