Viewing Study NCT03342248



Ignite Creation Date: 2024-05-06 @ 10:45 AM
Last Modification Date: 2024-10-26 @ 12:35 PM
Study NCT ID: NCT03342248
Status: UNKNOWN
Last Update Posted: 2017-11-14
First Post: 2017-11-08

Brief Title: Evaluation of the Impact of a Social Network Via a Digital Platform for Caregivers of Patients Suffering From Mental Disorders
Sponsor: Assistance Publique Hopitaux De Marseille
Organization: Assistance Publique Hopitaux De Marseille

Study Overview

Official Title: Evaluation of the Impact of a Social Network Via a Digital Platform for Caregivers of Patients Suffering From Mental Disorders
Status: UNKNOWN
Status Verified Date: 2017-11
Last Known Status: NOT_YET_RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: CONNECT
Brief Summary: Severe mental illnesses have a significant social cost as much by their impact on the sick as on their entourage The Deinstitutionalization and care in the community of patients with severe mental illness result in increased families and loved ones also known as informal caregivers or informal caregivers If psychoeducation programs have been developed to help caregivers better manage and cope with the illness of the person being helped optimize the quality of care manage anxiety and isolation these initiatives appear minimal in view of the magnitude of the burden notion of burden burden and the suffering of caregivers Quality of life levels remain extremely low compared to the general population nearly 4 out of 10 caregivers show a sense of inability to cope with the permanent anxiety of this load 13 feels depressed and over 110 feels isolated on a personal and professional level
Detailed Description: This project will take place in three stages

1- Development and development of the network the conception of the social network is based on the point of view of the caregivers which is one of the originalities of this project Current social networks are very medico-centric And often poorly adapted to the needs of caregivers of patients suffering from pathologies mental disorders This step is based on a qualitative approach to these caregivers Focus groups 5 focus of 5 carers will be led by a psychologist in order to understand their experience and identify the resulting needs in order to determine the architecture and services offered on the network social From emerging needs a study based on Delphi method will be conducted with professionals from different disciplines psychiatry public health communication and information professionals ethicists health economists and sociologists to provide a light on the professional responses that can be proposed to the needs of carers The development of the social network will be done in close collaboration with a caregiver who will be in charge of the animation and moderation of the network 2 Implementation of the randomized trial comparing two groups of caregivers access to the social network vs lack of access to the social network over a period of 6 month The same scales will be filled by both groups at T0 and then at 6 months

3 Qualitative approach to network perception semidirective interviews made by a psychologist to a panel of caregivers using the network at course of 6 months

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None