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Being Young : My Mental Health

A 12-month Prospective Cohort Study of Mental Health Care Pathways of Adolescents and Young Adults

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05886595
Acronym
JEMMA
Enrollment
400
Registered
2023-06-02
Start date
2023-09-04
Completion date
2026-08-31
Last updated
2023-06-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mental Disorder, Mental Health Issue

Keywords

mental health, adolescent, young adult, psychiatry

Brief summary

The goal of this prospective cohort study is to study the evolution of adolescent and young people's mental health over a 12-month period after presentation to an emergency department or crisis service for an acute psychiatric episode. This study aims to: * Describe the mental health care trajectories of adolescents and young adults after an acute psychiatric episode. * Identify psychiatric disorders (such as anxiety, depression, eating disorders, suicidal thoughts, sleep, etc.) at the different time points of the study (at 3, 6, 9 and 12 months after inclusion) ; * Assess the quality of life and functional capacity in daily activities of participants at each study time point ; * Determine the socio-demographic, psychosocial and environmental factors associated with improving mental health over time and with mental health help seeking. Patients aged from 10 to 24, presenting to one of the participating centers for an acute psychiatric episode, and who agree to participate, will be included in the study. Participants will have to complete an online questionnaire every 3 months over a 12-month period (at baseline (T0), at 3 months (T3), at 6 months (T6), at 9 month (T9) and at 12 months (T12))

Detailed description

Recruitment process A poster campaign will be carry out in all study locations. Patients aged between 10 and 25 visiting one of the study location will be invited to participate in the study. The clinical research associates will visit all study location on a weekly basis in order to present the study to eligible patients. After checking the inclusion criteria, the clinical research associate will call eligible patients (or their legal representative for patients under 18) to present the study, the implications related to study participation, and obtain their oral consent. Patients who were willing to participate in the study will be automatically identify by a number. Follow-up : Patients will have to complete an online questionnaire at different time of the study: at baseline, at 3 months, at 6 months, at 9 months and at 12 months. For the participants aged under 18, the questionnaire will have to complete by or with the help of the parental representative. Investigators will collect socio-demographic, clinical data related to the acute psychiatric episode, and health care pathway over time. Mental health assessments will be based on standardized questionnaires. Clinical research associates will send an email to all participants to complete the initial questionnaire (at baseline). Then, they will coordinate patient follow-up, and will send automatic reminder through email at the different times of the study :at 3 months (M3), 6 months (M6), 9 months (M9) and 12 months (M12) to complete the follow-up questionnaires online. Patients will be awarded a gift voucher worth €10 after each completed questionnaire.

Interventions

None listed

Sponsors

Groupement Interrégional de Recherche Clinique et d'Innovation
CollaboratorOTHER
Centre Hospitalier St Anne
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
10 Years to 24 Years
Healthy volunteers
Yes

Inclusion criteria

: All patients * aged from 10 to 24 years old * had an consultation in one the study locations for psychiatric reason

Exclusion criteria

: * Absence of consent of the patient or the parental authority holder (for minor patient) * Adult patients under legal protection * Lack of proficiency in French (language of the study)

Design outcomes

Primary

MeasureTime frameDescription
Strengths and Difficulties Questionnaire (SDQ)Baselinebrief emotional and behavioural screening questionnaire for children and young people Minimal value : From Not True Maximum value : Certainly True

Secondary

MeasureTime frameDescription
Suicidal Behaviors Questionnaire (SBQ)baselineSelf report questionnaire to identify risk factors for suicide in adolescents and adults. Scale from 0= I never had this thought to 6= Almost everyday
Ask Suicide-Screening Questions (ASQ)baselineScreening tool to identify individuals that require further mental health/suicide safety assessment at baseline Yes or No scale If patient answers No to all questions 1 through 4, screening is complete (not necessary to ask question #5) If patient answers Yes to any of questions or refuses to answer, they are considered a positive screen.
Addictive disordersbaselineQuestionnaire on alcohol and psychoactive substances consumption at baseline
Quality of Life, Enjoyment, and Satisfaction Questionnaire- (Q-LES-Q)baselineself-report measure designed to obtain sensitive measures of the degree of enjoyment and satisfaction experienced in various areas of daily functioning in adults at baseline 5-point scale from 1 (Very Poor) to 5 (Very Good)
Hospital Anxiety and Depression Scale (HADS)baselineMeasuring tool for anxiety and depression in a general medical population of patients at baseline 0-7 = Normal, 8-10 =Borderline abnormal (borderline case), 11-21 = Abnormal(case)
Sleep disordersbaselineQuestionnaire on difficulties that affect children and adults' sleep patterns at baseline
Patient healthcare trajectorybaselineQuestionnaire on the type of health care professional, the mental health care services visited,the frequency of medical appointments, the health events (hospitalization, emergency unit, suicide attempt) at baseline
social relation, social integration and social supportbaselinequestionnaire on difficulties related to social relation, social integration and social support affecting children and adult' mental health at baseline
sociodemographic , environmental and psycho social factorsbaselinesocio-demographic variables questionnaire (age, sex, education, household, employment or schooling, income, health insurance, medical history, psychiatric history if any) at baseline
Pediatric Quality of Life Enjoyment and Satisfaction Questionnaire (P-Q-LES-Q)baselineself-report measure designed to obtain sensitive measures of the degree of enjoyment and satisfaction experienced in various areas of daily functioning in children at baseline 5-point scale from 1 (Very Poor) to 5 (Very Good)

Countries

France

Contacts

Primary ContactIsabelle SABBAH-LIM, Pediatric psychiatrist
i.sabbah@ghu-paris.fr0143565779
Backup ContactAnne PEROZZIELLO, Epidemiologist
a.perozziello@ghu-paris.fr01.80.52.67.54

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026