Partnerships Between Schools and Public Mental Health Departments: Investigation of Multi-professional Interventions for Children Aged 3 to 8 With Mental Health Issues (Parpsych-Ed) (Parpsych-Ed)
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ClinicalTrials.gov Identifier: NCT04300712 |
Recruitment Status :
Not yet recruiting
First Posted : March 9, 2020
Last Update Posted : March 9, 2020
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Condition or disease | Intervention/treatment | Phase |
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School Difficulties Associated With Mental Health Problems | Behavioral: Questionnaires at the start and end of the school year | Not Applicable |
Study Type : | Interventional (Clinical Trial) |
Estimated Enrollment : | 2000 participants |
Allocation: | N/A |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Other |
Official Title: | Partnerships Between Schools and Public Mental Health Departments: Investigation of Multi-professional Interventions for Children Aged 3 to 8 With Mental Health Issues (Parpsych-Ed). |
Estimated Study Start Date : | September 1, 2020 |
Estimated Primary Completion Date : | December 31, 2021 |
Estimated Study Completion Date : | December 31, 2021 |

Arm | Intervention/treatment |
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Tracking of the children with difficulties
All parents and teachers will respond to the questionnaires and the beginning and end of school year which is not done in the routine for tracking the children in difficulty.
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Behavioral: Questionnaires at the start and end of the school year
Interventions will be proposed to children identified in a worrisome situation. The Strengths and Difficulties. Questionnaire will be used by teachers to score these situations. The recognition process of mental health problem and need continue with responses. Responses are supporting a graduated response process in school and facilitating external support when needed (mental health services, community supports). Early intervention is one of all responses, which involve caregivers. Responses to worrisome situations aim to improve schooling conditions, to acknowledge mental health problems or condition and the health services need for children. To evaluate the intervention, the impact supplement of SDQ and the follow-up questions will be used by the teachers and the parents of children who benefit of the intervention. The interventions will be experimented during year 2020-21. Children might benefit of them from several weeks to one year, according to their need.
Other Names:
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- number of 3 to 8 years old children identified with mental health services need [ Time Frame: 24 months ]Evolution of the number of 3 to 8 years old children identified with mental health services
- Strengths and Difficulties Questionnaire (SDQ) [ Time Frame: 12 months ]Changes in the impact supplement and the follow-up questions - parents and teachers
- Healthcare access, barriers to treatment, intervention acceptance [ Time Frame: 12 months ]Healthcare access, barriers to treatment, intervention acceptance
- Parent refusal rate to let their child benefit of all responses [ Time Frame: 12 months ]Parent refusal rate to let their child benefit of all responses
- Parent refusal rate to let their child benefit of the early intervention [ Time Frame: 12 months ]Parent refusal rate to let their child benefit of the early intervention
- Parents refusal rate to plan appointment in public health services as indicated after the intervention [ Time Frame: 18 months ]Parents refusal rate to plan appointment in public health services as indicated after the intervention
- Mental health and mental health services representation and use [ Time Frame: 18 months ]Changes in the mental health representations of parents, teachers and others professionnals

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Ages Eligible for Study: | 3 Years to 8 Years (Child) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
- Attending pre- and elementary schools involved in the ParpsychEd partnerships.
Exclusion Criteria:
- Absence of parents and/or child consent.

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04300712
Contact: Sandrine Bonneton, MD | 0033157278458 | bonnetonsandrine@gmail.com |
France | |
EPSM Barthélémy Durand | |
Grigny, Essone, France | |
EPSM de Guadeloupe | |
Saint-Claude, Guadeloupe, France | |
Contact: Caroll Devaux, MD caroll.devaux@epsm-guadeloupe.fr | |
EPSM Val de Lys | |
La Couture, Pas De Calais, France | |
Contact: Laurent Lauwerier, MD llauwerier@epsm-stvenant.fr | |
EPSM Val de Lys | |
Vieille chapelle, Pas De Calais, France | |
Contact: Laurent Lauwerier, MD llauwerier@epsm-stvenant.fr | |
Centre Hospitalier Sainte Anne | |
Paris, France | |
Contact: Marie-Odile Perouse de MontClos, MD perousedemontclos@ch-sainte-anne.fr | |
Sub-Investigator: Yann Cross, MD | |
Fondation Bon Sauveur de la Manche | |
Picauville, France | |
Contact: Justine Levaillant justine.levaillant@fbs50.fr | |
Centre Hospitalier de Saint Denis | |
Saint-Denis, France | |
Contact: Jean-Pierre Benoit jeanpierre.benoit@ch-stdenis.fr |
Study Director: | Jean-Luc Roelandt, MD | French World Health Organization Collaborating Centre for Research and Training in Mental Health | |
Principal Investigator: | Sandrine Bonneton, MD | French World Health Organization Collaborating Centre for Research and Training in Mental Health |
Responsible Party: | GCS pour la recherche et la formation en sante mentale |
ClinicalTrials.gov Identifier: | NCT04300712 |
Other Study ID Numbers: |
Parpsych-Ed_2018 |
First Posted: | March 9, 2020 Key Record Dates |
Last Update Posted: | March 9, 2020 |
Last Verified: | March 2020 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | Undecided |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
mental health children psychiatry school difficulties psychosocial interventions |