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MISAPSY: Childhood Maltreatment, Food Insecurity, Psychological Distress and Professional Integration Among Socioeconomically Disadvantaged Young Adults

NCT07427524 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2026-07-01
Last updated
2026-05-05

Condition(s) studied

Trauma and Stress-related DisordersFood InsecurityChild MaltreatmentPsychological DistressDepression SymptomsAnxiety Symptoms

Investigational drug(s) / intervention(s)

Food AssistancePsychological Follow-Up

Food Assistance: Weekly food assistance provided to participants for a duration of 12 months, aimed at reducing food insecurity.

Psychological Follow-Up: Twice-monthly psychological follow-up sessions provided over a 6-month period, delivered by trained psychodynamic psychologists, aiming to support psychological well-being and address trauma-related psychological distress.

Study summary

The MISAPSY study (Childhood Maltreatment, Food Insecurity, Psychological Distress and Professional Integration Among Socioeconomically Disadvantaged Young Adults) aims to model the complex interrelations between child maltreatment, trauma exposure, food insecurity, and psychological distress among precarious young adults enrolled in French youth employment and social integration services (Mission Locale).

Adopting a methodology structured around three complementary components, this study consists of: (1) a cross-sectional survey to identify key associations ; (2) a qualitative study based on semi-structured interviews exploring psychologists' subjective experiences, and (3) a longitudinal comparative interventional study involving two different support programs to assess and compare the impact of these interventions on participants' food insecurity and psychological well-being.

Using a multi-phase design, MISAPSY seeks to move beyond linear risk-factor models by adopting a systemic and network-based approach to mental health and social vulnerability. The study integrates quantitative analyses, including network analyses, qualitative exploration of professional practices, and comparative longitudinal intervention to inform more holistic, equitable, and transferable models of care for vulnerable young adults.

Eligibility

Sex
ALL
Min age
18 Years
Max age
25 Years
Healthy volunteers
No
Inclusion Criteria: * Be aged 18 to 25 years * Be supported by a Mission Locale in Paris as part of a social and/or professional integration program * Voluntarily participate in the study after receiving clear information and signing an informed consent form * Experiencing severe food insecurity (positive response to item 8 of the FIES) * Experiencing significant psychological distress, defined by: PHQ-9 score \> 15; GAD-7 score \> 10 * Have been exposed to at least one adverse childhood experience, identified via the CTQ-SF (Childhood Trauma Questionnaire - Short Form). Exclusion Criteria: * Being unable to provide informed consent due to impaired comprehension or communication skills * Currently receiving psychiatric care for an acute or chronic mental illness requiring regular specialized treatment * Experiencing a social or medical emergency incompatible with the study (e.g., unstable emergency housing, acute suicidal crisis, ongoing hospitalization) * Being incarcerated, under guardianship or curatorship without specific legal authorization to participate in research * Having previously participated in a similar study or currently being engaged in a structured psychological intervention protocol * Having insufficient command of the French language, preventing comprehension of instructions, questionnaires, or interviews.

Primary outcome measure(s)

Trial sites (6)

FacilityCityRegionStatus
Mission Locale site Centre Paris France
Mission Locale site Soleil Paris France
Mission Locale site Avenir Paris France
Mission Locale site Milord Paris France
Mission Locale site Est Paris France
Mission Locale site Pyrénées Paris France

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07427524 on ClinicalTrials.gov ↗ ← All trials in France