Subjective Experience of Antidepressant Prescription Among Adolescents With Anorexia Nervosa.
Maude Ludot-Grégoire, Vanille David, Emilie Carretier...
https://pubmed.ncbi.nlm.nih.gov/35444576/Actively Recruiting
Led by Assistance Publique - Hôpitaux de Paris · Updated on 2025-09-12
90
Participants Needed
1
Research Sites
30 weeks
Total Duration
Researchers are exploring how adolescents with anorexia nervosa, their parents, and healthcare professionals perceive and experience psychotropic drugs. This observational study aims to understand these experiences without preconceived ideas, focusing on the complexity of feelings and attitudes toward medications such as antidepressants and atypical antipsychotics in adolescent care. The study is conducted within an adolescent medicine department and involves interviews with these three groups. The study uses semi-structured interviews, including visual aids, to gather detailed personal experiences. Participants include adolescents aged 12 to 25 years with anorexia nervosa who have been prescribed psychotropic drugs, their parents, and healthcare professionals who treat these adolescents. Each participant will take part in an hour-long interview focusing on their views and experiences with these medications. Participants will be interviewed once on the day of inclusion in the study. Researchers will analyze these interviews to understand the subjective experiences related to psychotropic drug use in anorexia nervosa. This includes exploring reactions to medication proposals, actual use, and the impact these drugs have as seen by the individuals themselves and their families. The studys findings will help illuminate the complexities of drug treatment in adolescent anorexia nervosa.
CONDITIONS
Drugs Experience for Adolescents With Anorexia
M
Maude Ludot-Gregoire, MD, psychiatrist
M
Marie Benhammani-Godard
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
Assistance Publique - Hôpitaux de Paris
Lead Sponsor
URC-CIC Paris Descartes Necker Cochin
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Day of inclusion
Participants undergo semi-structured interviews to explore their experiences with psychotropic drugs.
1 interview visit (in-person or remote)
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
Have more questions? Get in touch with our team for quick support
Maude Ludot-Grégoire, Vanille David, Emilie Carretier...
https://pubmed.ncbi.nlm.nih.gov/35444576/Assistance Publique - Hôpitaux de Paris
Lead Sponsor
URC-CIC Paris Descartes Necker Cochin
Collaborating Sponsor