Qualitative Evaluation of Therapeutic Alliance in Adolescent Psychiatry
NCT ID: NCT03288649
Last Updated: 2024-08-23
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
129 participants
OBSERVATIONAL
2016-01-01
2021-06-30
Brief Summary
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Objective: to explore, within a qualitative approach, how a therapeutic alliance is established in three different clinical situations according to the adolescents, their parents and their physicians by crossing their perspectives.
Methods: This is a national (France) multi-center qualitative study based on 180 semi-structured interviews. Participants (purposively selected until data saturation) came from three different sub-samples: (i) adolescents with anorexia nervosa (N =20) plus their parents (N=20) and their physicians (N=20), (ii) adolescents with depressions (N=20) plus their parents (N=20) and their physicians (N=20), and (iii) adolescents with anxiety-based school refusal (N=20) plus their parents (N=20) and their physicians (N=20). Data are collected through open ended semi structured interviews and independently analyzed with NVivo V.11 software by three researchers according to the principles of Interpretative Phenomenological Analysis.
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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Anorexia nervosa
adolescents with anorexia nervosa (N=20 ?), their parents (N=20), their physicians (N=20)
No interventions assigned to this group
Anxiety based school refusal
adolescents with anxiety based school refusal (N=20 ?), their parents (N=20), their physicians (N=20)
No interventions assigned to this group
Depression
adolescents with depression (N=20 ?), their parents (N=20), their physicians (N=20)
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
1. refusal to attend school (to operationalize this first criterion, adolescents were included if they had not attended school at all for at least one month before starting treatment); (2) presence of a DSM-5 anxiety disorder (except obsessive-compulsive or post-traumatic stress disorders) with emotional upset at the prospect of attending school; (3) absence of a DSM-5 conduct disorder; and (4) parental knowledge of the adolescent's whereabouts during the period of non-attendance.
that led to treatment that had begun at least six months earlier and clinically determined to be well enough to participate in a research interview.
* receiving treatment for at least 6 months
* one parent at least agrees to participate
Exclusion Criteria
12 Years
18 Years
ALL
No
Sponsors
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Centre Hospitalier Victor Dupouy
OTHER
Responsible Party
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Anne Revah-Levy
Pr Anne Revah-Levy
Principal Investigators
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Anne Revah-Levy, MD PhD
Role: PRINCIPAL_INVESTIGATOR
Paris diderot University
Locations
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CHVictorDupouy
Argenteuil, , France
CHU Rouen
Rouen, , France
Countries
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Other Identifiers
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20140600001072
Identifier Type: -
Identifier Source: org_study_id
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