IPS_FIRAH: Self and Body-esteem in Socio-professional Rehabilitation

Sponsor
Hôpital le Vinatier (Other)
Overall Status
Recruiting
CT.gov ID
NCT04436757
Collaborator
(none)
56
1
2
35.3
1.6

Study Details

Study Description

Brief Summary

The body esteem influences the physical appearance, which can be a social brake. To enhance the socio-professional insertion of persons with severe mental disorders, the investigators developed a group program about self-presentation and body esteem. The study's objective is to understand the body esteem impact on socio-professional insertion, and how to improve that with a dedicated group program, for patients in a psychosocial rehabilitation center

Condition or Disease Intervention/Treatment Phase
  • Behavioral: IPS program : Self-image and body representation
  • Behavioral: TAU
N/A

Detailed Description

Our hypothesis is that a group program centered on the image and the presentation of the self, with the intervention of professionals of the image of the body, such as socio-hairdresser, socio-beautician, allows a better socio-professional inclusion, through an improvement in body self-esteem. Taking care of yourself will require different approaches such as advice on hygiene, becoming aware of your body, experimenting with beauty treatments and having the means to reproduce them at home. We will compare our IPS program (Image and Presentation of Self), with the usual management in the care center (TAU = "Treatment As Usual")

Study Design

Study Type:
Interventional
Anticipated Enrollment :
56 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized, single-centre, comparative, interventional study, treated in open parallel groups, measuring the impact of "professional" body image intervention on improving body self-esteem in patients with severe mental health problems.Randomized, single-centre, comparative, interventional study, treated in open parallel groups, measuring the impact of "professional" body image intervention on improving body self-esteem in patients with severe mental health problems.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Group Program IPS: Body-esteem and Self-esteem in a Psycho-social Rehabilitation Perspective
Actual Study Start Date :
Jun 22, 2020
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Jun 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: IPS (Self-image and body-representation program)

The IPS program (Self-image and body representation) was designed by Dr PLAZAT and coll. for specific use with patients with severe mental disorders suffering of low self- and body-esteem and aiming at " reinsert themselves" in the society.

Behavioral: IPS program : Self-image and body representation
The IPS program consists in 13 sessions of 2 hours over a 13-weeks period. Sessions content is as follows : : Introduction : Sensory approach workshop : Self presentation and personal hygiene : Organisation of well-being, planning and pictograms : Becoming aware of my body, my envelope : Presentation and self-esteem (photolanguage) : Self-presentation in social interactions: Social codes : My ideas and desires for change : Places of well-being and clothing hygiene : Vocational insertion devices : Daring change : presence of a Socio-hairdresser : The awakening of color : presence of a Socio-aesthetician : Development of practice sheets and the network

Active Comparator: TAU

Treatment As Usual : the usual care proposed by the health service (SUR/CL3R).

Behavioral: TAU
The treatment of the group TAU (Treatment As Usual) will consist of the usual care proposed by the health service. No additional session will be proposed.

Outcome Measures

Primary Outcome Measures

  1. Appreciation of one's own appearance [baseline, one month, three months, nine months after the end of the treatment]

    The main judgement criterion is the difference before/after the program for each of the two groups (IPS and TAU) of the weighted average at the "satisfaction with overall appearance" and "wish to change appearance" dimensions of the BES (Body-Esteem Scale), common dimensions for men and women. This difference will be compared between the 2 groups by a Student test (or a Wilcoxon-Mann-Whitney test in case of non normality).

Secondary Outcome Measures

  1. Appreciation of the Self-esteem measured by the Self-Esteem Rating Scale [baseline, one month, three months, nine months after the end of the treatment]

    As for the primary outcome

  2. Appreciation of the well-being measured by the Warwick-Edinburgh Well-Being Mental Scale [baseline, one month, three months, nine months after the end of the treatment]

    As for the primary outcome

  3. Appreciation of the satisfaction level measured by the Client's Assessment of Strengths, Interests and Goals Scale (CASIG ) [baseline, one month, three months, nine months after the end of the treatment]

    As for the primary outcome

  4. Appreciation of the satisfaction measured by the Satisfaction in the domains of life [baseline, one month, three months, nine months after the end of the treatment]

    As for the primary outcome

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Age 18 to 65.

  • Speaking French.

  • Diagnosis of severe mental disorders (MSD) established according to the criteria of the DSM-V (Diagnostic and Statistical Manual of Mental Disorders) such as: Schizophrenia, Bipolar Disorders, Serious Personality Disorders, Severe Anxiety Disorders, Depressive Disorders; with a clinical stability of more than 3 months.

  • Supported at SUR/CL3R with an application for socio-professional reintegration.

  • Guardian agreement (for persons under guardianship);

  • Information given to the curator (for persons under curatorship);

  • Member of the social security scheme.

Exclusion Criteria:
  • Diagnosis of Autism Spectrum Disorder (ASD) or Eating Behaviour Disorder.

  • Clinical status incompatible with group activity.

  • Acute episode in progress.

  • Refusal to participate.

  • Simultaneous participation in a psycho-social rehabilitation program targeting image or self-esteem (general and/or body).

Contacts and Locations

Locations

Site City State Country Postal Code
1 centre de réhabilitation - Hôpital le Vinatier Lyon Rhône France 69006

Sponsors and Collaborators

  • Hôpital le Vinatier

Investigators

  • Principal Investigator: Lucie-Orianne PLAZAT, M.D, CENTRE HOSPITALIER LE VINATIER

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hôpital le Vinatier
ClinicalTrials.gov Identifier:
NCT04436757
Other Study ID Numbers:
  • 2020-A00777-32
First Posted:
Jun 18, 2020
Last Update Posted:
Aug 12, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hôpital le Vinatier
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 12, 2022