- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05833880
Use of Complementary and Alternative Medicine in Children and Adults With Atopic Dermatitis
Use of Complementary and Alternative Medicine in Children and Adults With Atopic Dermatitis: a Single-center Prospective Observational Study
Complementary and alternative medicine are increasingly used all around the world and more specifically in chronic diseases such as atopic dermatitis. Sociodemographic and disease determinants associated with their use remain unclear. Moreover, most of studies involved children and little data are available for adults.
The main objective of this study is to identify factors associated with complementary and alternative medicine use in children and adults suffering from atopic dermatitis. The secondary objectives are to determine the prevalence of complementary and alternative medicine use, the main forms used and their modalities of use, patients' motivations for using these therapies and sources of information.
Patients of all ages consulting for their atopic dermatitis at the dermatology or pediatric allergology department of Nancy University Hospital over a 6 months period will be asked to fill out a questionnaire about their pathology and their use of complementary and alternative medicine. This questionnaire will be collected before they leave the hospital.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Contact
- Name: Anne-Claire Bursztejn
- Phone Number: +33383157146
- Email: ac.bursztejn@chru-nancy.fr
Study Locations
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Nancy, France
- University Hospital Of Nancy
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Contact:
- Anne-Claire Bursztejn
- Phone Number: +33383157146
- Email: ac.bursztejn@chru-nancy.fr
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- All patients, adults or children, without age limit;
- Patients visiting the dermatology or pediatric allergology department of Nancy University Hospital;
- Patients with atopic dermatitis confirmed on clinical examination by the physician;
- Patients with a history of atopic dermatitis or newly diagnosed patients;
- Patient affiliated to a social security plan or beneficiary of such a plan;
- Patients who understand French and are able to complete a self-administered questionnaire or have the option of assistance in completing it.
Exclusion Criteria:
- Patient with at least one other dermatological pathology or non-atopic eczema (contact eczema, ...);
- Patient without a confirmed diagnosis of atopic dermatitis by a physician;
- Patient who has already completed the questionnaire during a previous consultation;
- Pregnant and breastfeeding women;
- Refusal of the patient or at least one of the parents for children;
- Patient placed under court protection, guardianship or curatorship;
- Patient deprived of liberty by a judicial or administrative decision.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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Atopic dermatitis patients
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Self-administered questionnaire regarding complementary and alternative medicine use
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Binary variable: use of complementary and alternative medicine (yes/no)
Time Frame: Baseline (J0)
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Binary variable: use of complementary and alternative medicine (yes/no), variable collected by questionnaire, as reported by the patient (or the patient's parents)
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Baseline (J0)
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Percentage of patients using complementary and alternative medicine in relation to the total number of patients included in the study
Time Frame: Baseline (J0)
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Percentage of patients using complementary and alternative medicine in relation to the total number of patients included in the study, variable collected by questionnaire according to the patient's declaration (use or not use of complementary and alternative medicine) and then calculated
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Baseline (J0)
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Forms of complementary and alternative medicine used
Time Frame: Baseline (J0)
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Forms of complementary and alternative medicine used, variable collected by questionnaire, as reported by the patient (or the patient's parents)
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Baseline (J0)
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Modalities of use of complementary and alternative medicine
Time Frame: Baseline (J0)
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Modalities of use of complementary and alternative medicine, variable collected by questionnaire, as reported by the patient (or the patient's parents)
|
Baseline (J0)
|
Patients' motivations for using complementary and alternative medicine
Time Frame: Baseline (J0)
|
Patients' motivations for using complementary and alternative medicine, variable collected by questionnaire, as reported by the patient (or the patient's parents)
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Baseline (J0)
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Sources of information regarding complementary and alternative medicine
Time Frame: Baseline (J0)
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Sources of information regarding complementary and alternative medicine, variable collected by questionnaire, as reported by the patient (or the patient's parents)
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Baseline (J0)
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Anne-Claire Bursztejn, University Hospital of Nancy, France
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- 2023-A00605-40
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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