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Completed

NCT Number: NCT03235011

Evaluation of Knowledge Among Adolescents With Sickle Cell Disease.

Evaluation of knowledge about contraception in sickle cell adolescents.

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Key information

Conditions

Sickle Cell Disease Anemia Anemia, Hemolytic Anemia, Hemolytic, Congenital Anemia, Sickle Cell Congenital, Hereditary, and Neonatal Diseases and Abnormalities Genetic Diseases, Inborn Hematologic Diseases Hemic and Lymphatic Diseases Hemoglobinopathies

Age range

14 year–19 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Centre Hospitalier Intercommunal de Créteil

Créteil, Creteil, 77500, France

About this study

Sickle cell teenagers receive regular hospital medical care.

Adolescence is the time when the pathophysiology of the disease is re-explained and when questions around puberty (possibly delayed), sexuality and contraception are discussed.

Sickle cell disease, like any chronic disease, can have repercussion on the development and behavior of young patients.

Knowledge and understanding of young patients with sickle cell disease around these issues may be insufficient.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with sickle cell disease followed at the CHIC
  • Aged 14 to 19
  • Both sexes

Exclusion criteria

  • Neurological disorders that can impede understanding of the questionnaire.
  • Refusal to participate.
  • Not affiliated to social security.

Treatment and study plan

Primary outcomes

  1. Score value of the questionnaire on general knowledge on contraception

    Time frame: at inclusion

    questionnaire on general knowledge on contraception rated by 4 questions

Secondary outcomes

  1. Score value of the questionnaire on specific knowledge on the transmission of the disease

    Time frame: at inclusion

  2. Score value of the questionnaire on the transmission of the disease knowledge

    Time frame: at inclusion

  3. Score value of the questionnaire on specific knowledge about the impact of sickle cell disease on the course of puberty

    Time frame: at inclusion

  4. Score value of the questionnaire onspecific knowledge about the impact of sickle cell disease on the course of sexuality

    Time frame: at inclusion

  5. age of the patient with sickle cell disease

    Time frame: at inclusion

  6. gender of the patient with sickle cell disease

    Time frame: at inclusion

  7. number of hospitalizations of the patient with sickle cell disease

    Time frame: at inclusion

Sponsors and collaborators

Lead sponsor

Adele CARLIER-GONOD

Other

Registry information

Official study title

Evaluation of Knowledge and Practices About Contraception, Sexuality and Transmission Among Adolescents With Sickle Cell Disease.

Acronym: SEXODREP

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Aug 1, 2017
Registry last updated
Feb 6, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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