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Disclosure of research results

A randomized study on Genepso ‐ PS cohort participants

Bibliographic Data

ID19508329
AuthorsJason Mancini (0000-0001-9500-8598, Aix Marseille Université UMR_S912 IRD SESSTIM Marseille France, corresponding author), Julien Mancini, Elodie Le Cozannet (Aix Marseille Université UMR_S912 IRD SESSTIM Marseille France), Anne-Deborah Bouhnik (0000-0002-5418-4592, Inserm), Anne‐Déborah Bouhnik (Aix Marseille Université UMR_S912 IRD SESSTIM Marseille France), Noémie Resseguier (0000-0003-0816-4053, Aix Marseille Université UMR_S912 IRD SESSTIM Marseille France), Christine Lasset (0000-0002-8052-5880, Centre Léon Bérard Lyon France), Emmanuelle Mouret‐fourme (Institut Curie Hôpital René Huguenin Saint‐Cloud France), Catherine Noguès (Institut Curie Hôpital René Huguenin Saint‐Cloud France), Claire Julian‐reynier (Aix Marseille Université UMR_S912 IRD SESSTIM Marseille France)
Year2016
Volume19
Issue5
Pages1023-1035
Publication date2016-10-01
Open AccessYes
TypeARTICLE
VenueHealth Expectations (JOURNAL)
Journal identifiersISSN: 1369-6513 • E-ISSN: 1369-7625
PublisherWiley (PUBLISHER • GB)
DOI10.1111/hex.12390
PMID26205609
OpenAlexW1485842333
LanguageEN
References cited28

BACKGROUND: There exist no recommendations as to how aggregate research results should best be disclosed to long-term cohort participants. OBJECTIVE: To study the impact of cohort results disclosure documents of various kinds on participants' satisfaction. DESIGN: Randomized study with a 2x2 factorial design. SETTING AND PARTICIPANTS: The GENEPSO-PS cohort is used to study the psychosocial characteristics and preventive behaviour of both BRCA1/2 carriers and non-carriers; 235 participants wishing to receive 'information about the survey results' answered a self-administered questionnaire. INTERVENTIONS: The impact of providing the following items in addition to a leaflet about aggregate psychosocial research results was investigated (i) an up-to-date medical information sheet about BRCA1/2 genetic topics, (ii) a photograph with the names of the researchers. MAIN OUTCOME MEASURES: Satisfaction profiles drawn up using cluster analysis methods. RESULTS: Providing additional medical and/or research team information had no significant effect on satisfaction. The patients attributed to the 'poorly satisfied' group (n = 60, 25.5%) differed significantly from those in the 'highly satisfied' group (n = 51, 21.7%): they were younger [odds ratio (OR) = 0.96, 95% confidence interval (0.92-0.99), P = 0.028], less often had a daughter [OR = 4.87 (1.80-13.20), P = 0.002], had reached a higher educational level [OR = 2.94 (1.24-6.95), P = 0.014] and more frequently carried a BRCA1/2 mutation [OR = 2.73 (1.20-6.23), P = 0.017]. CONCLUSIONS: This original approach to disclosing research results to cohort participants was welcomed by most of the participants, but less by the more educated and by BRCA1/2 carriers. Although an easily understandable document is necessary, it might also be worth providing some participants with more in-depth information

Cohort · Cohort study · Confidence interval · Family medicine · Odds ratio · Patient satisfaction · Psychiatry · Psychosocial · Randomized controlled trial · BRCA gene mutations in cancer · Ethics in Clinical Research · Medicine · Meta-analysis and systematic reviews · Nursing · Psychology · Internal Medicine

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