Impact of Caregiver Beliefs on Adherence to Antipsychotic Medications in Patients With Schizophrenia

NCT ID: NCT03471013

Last Updated: 2019-02-04

Study Results

Results pending

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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Recruitment Status

UNKNOWN

Total Enrollment

150 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-03-20

Study Completion Date

2019-03-30

Brief Summary

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Only one third of patients with schizophrenia are observant to their treatment knowing that the lack of adherence to treatment is one of the most important predictors of relapse.

Recent work shows that the erroneous or negative beliefs of patients with schizophrenia regarding antipsychotic treatment are associated with poor compliance.

The hypothesis is that negative beliefs about the antipsychotic treatment of caregivers of patients with schizophrenia may be associated with a higher risk of poor compliance compared to caregivers with positive beliefs about treatment.

The primary purpose is to explore the correlation between caregiver beliefs about treatment and patient compliance, taking into account the level of caregiver-patient link.

Detailed Description

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Non-interventional cross-sectional exploratory study with a single visit for patients with schizophrenia and their caregivers, who agreed to participate in the protocol.

Conditions

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DSM-5 Schizophrenia

Study Design

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Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Patients and caregivers

Patients suffering from schizophrenia accompanied by their caregiver

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Patient over 18 years old
* With a diagnosis of schizophrenia according to DSM-5 criteria
* Accompanied by his main caregiver, who will be able to complete the questionnaires after having signed the information form.
* Treated with one or more antipsychotics.
* Able to complete the questionnaires related to the protocol
* Having agreed to sign the information form.

Exclusion Criteria

* Not understanding French, unable to answer questions linguistically
* Presenting an organic pathology and / or cognitive deterioration likely to hinder a good understanding of the interview
* Having already participated in the study
* presenting disorders related to the use of substances of severe intensity (such as acute intoxication, withdrawal syndrome or any state of delirium)
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Clermont-Ferrand

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Ludovic SAMALIN

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Clermont-Ferrand

Locations

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Chu Clermont-Ferrand

Clermont-Ferrand, , France

Site Status RECRUITING

Countries

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France

Central Contacts

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Patrick LACARIN

Role: CONTACT

0473751195

Facility Contacts

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Patrick LACARIN

Role: primary

0473751195

Other Identifiers

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2017-A02271-52

Identifier Type: OTHER

Identifier Source: secondary_id

CHU-384

Identifier Type: -

Identifier Source: org_study_id

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