- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05678478
Perceptions,Social Representations and Experience of Lyme Borreliosis and Ticks in Adolescents Likely to be Infected and Their Parents (ADO-LY)
the study is offered to adolescents aged 12 to 17 and their families suspected of or suffering from Lyme barilliosis.
During inclusion, three interviews will be carried out for each family. This choice of the number of interviews per family seems the most appropriate to have a plurality of answers to the questions asked. Thus, these will have a duration of 30 min to 1 hour and will be carried out by an anthropologist. The first interview will be with the teenager. The second interview will then concern the parent(s). Finally, the last appointment will be with the teenager and his parents.
Study Overview
Status
Conditions
Detailed Description
the study is offered to adolescents aged 12 to 17 and their families suspected of or suffering from Lyme barilliosis.
During inclusion, three interviews will be carried out for each family. This choice of the number of interviews per family seems the most appropriate to have a plurality of answers to the questions asked. Thus, these will have a duration of 30 min to 1 hour and will be carried out by an anthropologist. The first interview will be with the teenager. The second interview will then concern the parent(s). Finally, the last appointment will be with the teenager and his parents.
After a few introductory questions concerning the socio-demographic characteristics of adolescents, their medical history and their exposure to ticks, the anthropologist will ask the semi-open questions.
As for the parent(s), the anthropologist will ask them questions directly related to Lyme borreliosis and the tick. Finally, questions will be proposed simultaneously during a joint interview with the teenager and his parents.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Crosne, France, 91560
- Centre Hospitalier Intercommunal Villeneuve Saint Georges
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Paris, France, 75012
- Hôpital Armand Trousseau AP-HP
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Be at least 12 years old and maximum 17 years old.
- Be accompanied by a holder of parental authority
- Live in metropolitan France.
- Suspect or have Lyme borreliosis
- Non-objection for participation in the protocol
Exclusion Criteria:
- Refusal of participation of a holder of parental authority and of the adolescent
- Non-mastery of oral French by the teenager or his parents
- Protected persons (patients under guardianship or curatorship, pregnant or nursing women, persons deprived of liberty, person unable to express their non-objection)
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Story of the teenager and one of his parents or both parents
Time Frame: Baseline
|
analysis and identification of perceptions, representations and experiences of adolescents and their parents on Lyme borreliosis and ticks
|
Baseline
|
Collaborators and Investigators
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
- ADO-LY
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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