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NCT Number: NCT07317388

Group Psychoeducation to Promote Independent Living in Individuals With Psychiatric Disorders

This study evaluates the effectiveness of group psychoeducation for users and carers to help people with severe psychiatric disorders achieve autonomy at home.

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Key information

Conditions

Psychiatric Disorder Behavior Mental Disorders Personal Satisfaction Psychological Well-Being

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

EPS VIlle Evrard - UNIRRE 93

Neuilly-sur-Marne, France

Location status: Recruiting

Location contact

Raluca Rosetti

CONTACT

[email protected]

+33613616270

About this study

The study will assess the autonomy of users with severe psychiatric disorders in a home setting before and after participation in the psychoeducation group. The program includes 10 sessions focusing on various aspects of daily living and cognitive functions.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Volunteer for a home autonomy project
  • Management of a mental health problem (mood disorder or psychotic disorder)
  • Consent for participation (non-opposition)
  • Taken care by the RPS 93 platform

Exclusion criteria

  • Acute clinical state

Treatment and study plan

Primary outcomes

  1. Life Habits Assessment Tool

    Time frame: Baseline, at the end of the 10-week AUTON'HOME psychoeducation program, and 3 months after program completion

    Assessing the autonomy of users with severe psychic pathologies in housing before and after participation in the psychoeducation group.

Secondary outcomes

  1. Center for Epidemiologic Studies Depression Scale

    Time frame: Baseline, at the end of the 10-week AUTON'HOME psychoeducation program, and 3 months after program completion

    Assesses emotional impressions and depressive symptoms in caregivers.

  2. Zarit Burden Interview Scale

    Time frame: Baseline, at the end of the 10-week AUTON'HOME psychoeducation program, and 3 months after program completion

    Quantifies caregiver burden.

  3. Family Expectations Questionnaire

    Time frame: Baseline (prior to initiation of the AUTON'HOME psychoeducation program)

    It aims to collect the expectations of family members regarding the autonomy and daily functioning of their loved one living with a severe mental disorder.

  4. Family Expectations Fulfillment Questionnaire

    Time frame: At the end of the 10-week AUTON'HOME psychoeducation program and 3 months after program completion

    It evaluates whether the expectations previously expressed by the family have been fulfilled, partially met, or unmet.

  5. Positive and Negative Syndrome Scale

    Time frame: Baseline and 3 months after completion of the 10-week AUTON'HOME psychoeducation program

    Measures severity of psychiatric symptoms.

  6. Clinical Global Impression

    Time frame: Baseline and 3 months after completion of the 10-week AUTON'HOME psychoeducation program

    Assesses global improvement compared to baseline.

  7. Montreal Cognitive Assessment

    Time frame: Baseline and 3 months after completion of the 10-week AUTON'HOME psychoeducation program

    Screens for mild to moderate cognitive impairments.

Study contacts

Contact information is provided by the study sponsor or research team.

Youcef BENCHERIF, Clinical Project Manager

CONTACT

[email protected]

01.43.09.32.32

Sponsors and collaborators

Lead sponsor

Centre hospitalier de Ville-Evrard, France

Other

Registry information

Official study title

Study on the Effectiveness of Group Psychoeducation (for Users and Caregivers) in Promoting Autonomy at Home for Individuals With Psychatric Disorder.

Acronym: AUTON'HOME

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Jan 5, 2026
Registry last updated
Jan 5, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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