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UnknownNCT05813756

Validation Study of the Coping, Motivation and Post-diagnosis Psychoeducation Program for Adults With Autism

Validation Study of the Coping, Motivation Ans Post-diagnosis Psychoeducation Program for Adults With Autism : a Randomized Controlled Trial

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
66 (estimated)
Sponsor
Centre Hospitalier Rouffach · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary objective of the study is to evaluate the effectiveness of a post-diagnostic psychoeducational intervention in increasing the sense of self-efficacy of adults diagnosed with Autism Spectrum Disorder-Without associated Intellectual Disability

Detailed description

Secondary objectives The other objectives of this study are : 1. To evaluate the effectiveness of the intervention on self-esteem ; 2. To evaluate the effectiveness of the intervention on anxiety-depressive symptomatology ; 3. To evaluate the effectiveness of the intervention on the acceptance of the diagnosis ; 4. To evaluate the acceptance of the intervention. Conduct of research The study will be offered to individuals diagnosed with autism spectrum disorder without associated intellectual developmental disabilities in adulthood. After signing the consent form and verifying the eligibility criteria, participants will be randomized into the waiting list group or the intervention group. In the intervention group : the participant will receive 10 one-hour individual sessions, bi-monthly, with an assessment at midterm (T1 : T0+\~2.5 months), at the end of the intervention (T2 : T0 +\~5 months) and 3 months after the intervention (T3 : T0 +\~8 months). In the waiting list group : the participant will receive the intervention at the exit of the research protocol (after T3). At conclusion and at each visit, participants will complete questionnaires and scales defined in the protocol.

Conditions

Interventions

TypeNameDescription
OTHERPost-diagnosctic psychoeducational interventionParticipants are randomized to the intervention group. In this group, the participant receives 10 one-hour individual sessions of psychoeducational intervention, bi-monthly, with an evaluation at mid-term (T1:T0+\~2.5 months), at the end of the intervention (T2 : T0+\~5 months) and 3 months after the intervention (T3 : T0+\~8 months). At the same time psychological questionnaires and scales will be completed

Timeline

Start date
2023-03-20
Primary completion
2024-10-30
Completion
2024-12-30
First posted
2023-04-14
Last updated
2023-04-14

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT05813756. Inclusion in this directory is not an endorsement.