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Impact of a Psychoeducational Intervention on Expectations and Coping in Young Women Exposed to a High HBOC Risk

Impact of a Psychoeducational Intervention on Expectations and Coping in Young Women (18-40 Years) Exposed to a High Familial Breast/Ovarian Cancer Risk

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02705924
Enrollment
32
Registered
2016-03-11
Start date
2016-04-30
Completion date
2021-09-14
Last updated
2021-11-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hereditary Breast and Ovarian Cancer Syndrome

Brief summary

Young female counselees (18-40 years) belonging to HBOC families with a known mutation on BRCA-genes or not, receive a lot of information regarding their cancer risk. Information sources are numerous and sometimes contradictory. Unfortunately, these women face these issues at a key moment of there identity construction (self, relationship, sexuality) while they are not yet concerned by health prevention measures. A special psychoeducational intervention was designed to help these women to better cope with these difficulties. Intervention consists in a week-end session in a thermal center (SPA) during which they will attend short conferences given by specialists (prevention measures, prophylactic surgery, assisted procreation, epidemiology...) and participate to role games and group sharing. Intervention will be evaluated using self-questionnaires completed before intervention and during the following year.

Detailed description

Background: Young women exposed to a high hereditary breast/ovaries cancer (HBOC) risk are particularly vulnerable: they are ignored by health prevention measures; they are embedded in a stream of contradictory information ( medicine, media, internet); they may feel concerned by surgical prevention issues at a key moment of there identity construction (self, relationship, sexuality). A special psychoeducational intervention was designed to help these women to better cope with these difficulties. Methods/design: the study consists in a prospective randomized trial including childless young female counselees (18-40 years) of CCC Jean Perrin oncogenetics department, belonging to HBOC families either BRCA-mutated or not. They will be invited to attend a weekend group session in a SPA resort and participate to a series of short expert conferences and to focus group activities (group sharing, Moreno role game) supervised by a psychotherapist. Two sessions separated by a 6-month delay (waiting list) will enable us to evaluate the intervention effect, by comparing the evolution of questionnaires scores between inclusion and 6-month post-intervention. Main end-point is an increase of the Hert Hope Inventory of at least one standard deviation. Secondary endpoints investigate self-esteem, anxiety-trait, anxiety-state, ways of coping and quality of life. Participants will be randomized 1:1 to the first or the second session so that groups are comparable. Session will be cost-free for participants.

Interventions

BEHAVIORALpsychoeducation

Participants will attend conferences where experts present the state of the art in various domains: * Latest knowledge in oncogenetics * Recommendations and morbidity of prophylactic breast surgeries and annexectomy * Epidemiology of HBOC and comparative mortality risks with other syndromes/life habits * How to perform the periodic breast screening * Assisted medical procreation and embryo selection * Importance of nutrition and physical activity as risk modulator * Life habits: how one can increase or lower the cancer risk (tobacco, alcohol...)? * Description of the assistance program (GENAUV) to help counselees exposed to a high cancer risk follow their medical screening. The remaining time after this information, i.e. about half of the week-end, will comprise group activities, in particular role games (Moreno psychodrama approach) and group sharing under the supervision of a psychotherapist.

Sponsors

Fondation de l'Avenir et la MASFIP, Paris - France
CollaboratorUNKNOWN
Centre Jean Perrin
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* Participants must belong to HBOC families, * aged between 18 and 40 years * Single or couple with a desire to have a child * without any personal history of cancer. * must have consulted at the oncogenetics department of the CCC Jean Perrin * tested for a BRCA mutation. * mutation carrier in case of a known familial BRCA mutation, else exposed to a high familial HBOC risk (Eisinger score ≥ 6 or Manchester score ≥ 16) * must live in Auvergne region (middle France) * signed an informed consent before inclusion.

Exclusion criteria

* pregnant women * person who cannot answer questionnaires: language difficulties and/or cannot write in French correctly. * no possible connection to our web-site * psychiatric troubles and/or ongoing treatments preventing from a week-end stay in a SPA resort

Design outcomes

Primary

MeasureTime frameDescription
changes in expectations measured using the Hert Hope Inventory questionnairechanges of global score from baseline to 6-month post-intervention.Hert Hope Inventory global score \[Herth, 1992, 2000\] is used to evaluate expectations of participants. It contains only 12 simple proposals quoted using a 4-point Likert scale ranking from 1 = strongly disagree to 4 = strongly agree. Its internal structure is composed of three dimensions: temporality and future, positive readiness and expectancy, and social/spiritual connectedness \[Farran, 1995\]. This questionnaire has been translated and validated in French by Lafrance \[2013\].

Secondary

MeasureTime frameDescription
Dimensions of coping evaluated by the Ways of Coping Checklist (WCC) [Folkman, 1980].inclusion - 6-month post-intervention - 1-year post-interventionThe WCC French version contains 27 items quoted by Likert scales (answers within no, rather no, rather yes, yes). Three specific dimensions are described: * the focus on the problem * the focus on emotions * the search for social support Dimensions will be used separately using their scores as no global score can be calculated (dimensions are divergent). This questionnaire has been validated in French in 1996 by Bruchon-Schweitzer et al.
Dimensions of perceived control measured using the Internal Powerful others and Chance scale (IPC) [Levenson, 1973].inclusion - 6-month post-intervention - 1-year post-interventionPerceived Control of IPC tests two locus of control: either in the self, or outside with two origins: fate/luck and powerful others. Scores qualifying each locus of control will be used for statistics. This 24-item scale has been validated in French by Loas et al. \[1994\].
Level of Anxiety, either fundamental (as a trait of character) or superficial (depending on circumstances) evaluated by the State and Trait Anxiety Inventory (STAI A-B) [Spielberger, 1983]inclusion - 6-month post-intervention - 1-year post-interventionThe STAI A-B questionnaire evaluates anxiety in a way it cannot be confused with depressive syndrome. It comprises 40 items rated on a 4-point scale from almost never to almost always. The 20 first ones evaluate the anxiety as a state, that is a labile/contextual form. The last 20 items estimate anxiety as a personality trait, independent of the environment. It has been translated and validated in French by Schweitzer & Paulhan \[1990\].
Score of the Self-Esteem Scale (SES) [Rosenberg, 1965]inclusion - 6-month post-intervention - 1-year post-interventionIt is a short 10-item questionnaire that evaluates the global self-worth by questioning positive and negative feelings about the self. The uni-dimensionality of the scale has been validated \[Gray-Little, 1997\]. The global score of the scale will be used as an indicator of self-esteem.
Subscales and global score of the WHO Quality of life questionnaire ( World Health Organization WHOQOL) [Harper, 1998].inclusion - 6-month post-intervention - 1-year post-interventionThis questionnaire is worldwidely used. It contains four main dimensions: physical health, psychological, social relationships and environment. These dimensions have been confirmed in the French version by Leplège et al. \[2000\]. The global QoL score (means of subscales) will also be used for statistics.

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 28, 2026