Evaluation of the Information Letter to Relatives in the Context of Genetic Assessments (LIPEG)
Přehled studie
Postavení
Detailní popis
The recent publication of the decree of June 20th 2013 (n° 2013-527) suggests a protocol regarding the transmission of information of the relatives after genetic diagnosis of a serious condition allowing preventative or care measures. In the case a mutation career refuses to directly inform other members of his family, option is to call on services of a genetic professional for the transmission of its family information. This decree includes a specific model of letter that can be sent to relatives by genetic professionals.
The main objective of the present study is the standardization of the procedure concerning the information to relatives by all genetic professionals. It would allow the same format of information in all families involved.
The first part (study 1a) evaluated the understanding and feelings after the reading of the decree's letter (letter A) on patients and the public, through the use of an individual and oral questionnaire. Interviews with the patients, public, genetic professionals and people who have received this letter completed the study 1a (study 1b). A focus group (accounting different genetic professionals and patient associations) composed a new version of letter (letter B) through these observations (study 1c).
The second part will compare the two letters model (A vs B) impact through precise items on three populations: patients, public and genetic professionals. This study will allow to:
- Evaluate how the letter composed by the focus group (letter A) is understood and perceived by the patients and the public with the same methodology as study 1a (study 2a) ;
- Compare the two letters model (A vs B) to describing the preference of patients, public and genetic professionals (study 2b).
The expected results would help us to choose the letter accommodating as many people as possible to standardize practices.
Typ studie
Zápis (Aktuální)
Kontakty a umístění
Studijní místa
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Montpellier, Francie, 34295
- CHRU de Montpellier - Hôpital Arnaud de Villeneuve
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Rennes, Francie, 35203
- CHU de Rennes - Hôpital Sud
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Toulouse, Francie, 31059
- CHU de Toulouse - Hôpital Purpan
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Aquitaine
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Bordeaux, Aquitaine, Francie, 33000
- University Hospital Bordeaux
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Strasbourg, Aquitaine, Francie, 67080
- Hôpital Universitaire de Strasbourg
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Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Metoda odběru vzorků
Studijní populace
- Group 2a-patient: 75 patients who attended a genetic counselling consultation.
- Group 2a-public: 75 persons belonging to the general population who never attended genetic counselling consultation.
- Group 2b-patient: 75 patients who attended a genetic counselling consultation.
- Group 2b-public: 75 persons belonging to general population who never attendeda genetic counselling consultation. These persons are different than persons from group 2a-person.
- Group 2b-professionnal: 75 genetic professionals (geneticist and genetic counsellor).
Popis
Inclusion Criteria:
- 18 years old and above
- French native speaker
- informed person
- person whose non-opposition has been received
- public: person who never attended a genetic counselling consultation
- professional: geneticist and genetic counsellors working in France
Exclusion Criteria:
- study 2a : person who took part of study 2b
- study 2b : person who took part of study 2a
Studijní plán
Jak je studie koncipována?
Detaily designu
Kohorty a intervence
Skupina / kohorta |
Intervence / Léčba |
|---|---|
|
Group 2a-patient
75 patients who attended a genetic counselling consultation.
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Oral questionnaire after the reading of letter B.
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|
Group 2a-public
75 persons belonging to general population.
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Oral questionnaire after the reading of letter B.
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|
Group 2b-patient
75 patients who attended a genetic counselling consultation (those patients are different than patients from group 2a-).
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Oral questionnaire after the reading of letter B.
Oral questionnaire after the reading of letters A and B during individual interview.
|
|
Group 2b-public
75 persons belonging to general population (those persons are different than patients from group 2a).
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Oral questionnaire after the reading of letter B.
Oral questionnaire after the reading of letters A and B during individual interview.
|
|
Group 2b-professional
75 genetic professionals.
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Oral questionnaire after the reading of letter B.
Oral questionnaire after the reading of letters A and B during individual interview.
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Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Časové okno |
|---|---|
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Score of understanding questionnaire after reading letter B.
Časové okno: 1 day
|
1 day
|
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Proportion of persons who prefer the letter B.
Časové okno: 1 day
|
1 day
|
Spolupracovníci a vyšetřovatelé
Sponzor
Vyšetřovatelé
- Vrchní vyšetřovatel: Cécile ZORDAN, Ms, University Hospital, Bordeaux
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia
Primární dokončení (Aktuální)
Dokončení studie (Aktuální)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Odhad)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Odhad)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
Další identifikační čísla studie
- CHUBX 2014/32
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