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OpenTrials
Completed

NCT Number: NCT04423809

Impact of Burden in Caregivers of Patients Hospitalized for a Psychotic Episode: a Multicenter Study

Family support is a positive predictor for psychiatric patients. For example, since the 1980s, it has been shown that family psychoeducation improves patient adherence to care and statistically decreases patient relapse and hospitalization rates by half, resulting in lower care costs. Yet, the stress of hospitalizing a patient, seeing the feelings of shame or guilt of caregiver and the impact on their quality of life are rarely taken into account by caregivers during the first weeks hospitalization in a patient's psychiatry.

Barrelet emphasizes the importance of organizing the meeting in the first hours of hospitalization with the family in order to strengthen the alliance, to improve communication.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Unité de recherche clinique

Neuilly-sur-Marne, Île-de-France Region, 93330, France

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Family members or relatives
  • Over 18 years
  • Having a relative
  • First hospitalized in psychiatry or hospitalized in psychiatry within 5 years
  • Over 18 years of age
  • Psychotic episode
  • Having been informed of their participation in this study
  • In regular contact with the patient prior to hospitalization, at least 4 hours per week.
  • French language
  • Signed written informed consent.

Exclusion criteria

-Psychiatric pathology of another family member than the hospitalized.

Treatment and study plan

Clinical Assessment

Other

assessment of caregivers suffering when a family member is hospitalized

Other names: Interview

Primary outcomes

  1. Center for Epidemiologic Studies-Depression scale

    Time frame: at patient admission

    is a simple tool for assessing depressive symptomatology for the general population

Secondary outcomes

  1. Zarit burden inventory

    Time frame: at patient admission

    to assess burden

  2. Short form 36

    Time frame: at patient admission

    To assess quality of life

  3. Semi-directional interview

    Time frame: At patient admission

    It consists of five items: subjective feeling, quality of life, social life, mood of the caregiver.

Sponsors and collaborators

Lead sponsor

Centre hospitalier de Ville-Evrard, France

Other

Registry information

Acronym: AFP

Important dates

Study start
2015
Primary completion
2018
Study completion
2020
First posted
Jun 9, 2020
Registry last updated
Jun 9, 2020

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.