Mental Disorder

38

Review clinical trials related to Mental Disorder. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

CapExchange: A Pilot Feasibility Study of a Capacity-Exchange Programme for Mental Health Recovery

CapExchange is a psychosocial rehabilitation programme based on reciprocal exchange of capacities and services between service users and their community environment, grounded in the concepts of circular mutuality and micro-social contribution. This pilot feasibility study aims to assess the feasibility and acceptability of the programme within the Psychosocial Rehabilitation Service of the EPSM de la Guadeloupe, across three sites: the Unité Passerelle, the CATTG Doubs, and the UREPS outpatient unit. A sample of 10 to 15 adult service users with a stabilized mental disorder is targeted. The intervention comprises five weekly group sessions of 75 minutes. Primary measures include the Social Contribution Score (SCS) and the Warwick-Edinburgh Mental Well-being Scale (WEMWBS).

Participants needed: 15
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: EPSM de la GuadeloupeUpdated: Jun 29, 2026Locations: 1
Eligibility criteria

Adults aged 18 years or over [+3]

Severe clinical instability at the time of inclusion [+3]

Status: Recruiting

Virtual Menstrual Pain Approaches in Females

This research study is testing two self-care approaches that may help prevent or reduce period pain in young females with recurrent painful menstrual cramps. Participants will be placed by chance into 1 of 3 groups: auricular acupressure, Baduanjin qigong, or a self-care education comparison group. The auricular acupressure and Baduanjin groups will receive online training and then practice the treatment on their own for 12 weeks. The main question is whether these two approaches can reduce the severity of menstrual pain. The study will also look at whether they can improve other symptoms that often happen with period pain, such as tiredness, poor sleep, anxiety, low mood, trouble concentrating, and reduced physical function. Researchers will also study stool and blood-related biological markers to better understand whether changes in gut bacteria and body metabolism may be linked to symptom improvement. A total of 145 participants will take part in the study at NTU, and any side effects or other safety concerns will be checked every week.

Participants needed: 145
Trial details
Phase: Phase 2, Phase 3Age: 16-35Biological sex: FemaleType: InterventionalSponsor: Nanyang Technological UniversityUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

16 - 35 years of age [+5]

Uncontrolled neurological diseases, immunodeficiency, bleeding disorders, and al... [+4]

Status: Not yet recruiting

Project Yes+ for Young MSM Living With HIV in Vietnam

In Vietnam, adolescent and young men who have sex with men (AYMSM) are among those most affected by HIV, and they also experience significant HIV-related mental health and stigma challenges. The study team proposes to adapt Project YES+ to address both mental health and internalized HIV stigma among AYMSM living with HIV in Vietnam. This research will build local capacity and develop networks for collaborative research on mental health and stigma in this population between Vietnam, Zambia and the United States.

Participants needed: 80
Trial details
Age: 16-24Biological sex: MaleType: InterventionalSponsor: Hanoi Medical UniversityUpdated: Jun 9, 2026Locations: 1
Eligibility criteria

16-24 years old Vietnamese; [+5]

Being currently enrolled in another HIV intervention; [+1]

Status: Recruiting

Preliminary Efficacy Trial of a Digital Intervention for Depression and Cannabis Use

The purpose of this study is to examine the feasibility, acceptability, and preliminary efficacy of a digital intervention for co-occurring cannabis use and depression. Participants will be randomized to complete Amplification of Positivity - Cannabis Use (AMP-C) or symptom tracking. The main outcomes will include changes in depressive symptoms and cannabis use, as well as usability ratings.

Participants needed: 80
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Massachusetts General HospitalUpdated: Jun 2, 2026Locations: 1
Eligibility criteria

Aged ≥ 18 years [+7]

History of a psychotic disorder or bipolar disorder type I/II [+3]

Status: Recruiting

Integrated Mental Health Care for Pregnant Women With HIV in Kenya: The Tunawiri Study

This study seeks to improve mental health, pregnancy, and HIV outcomes among pregnant and postpartum women living with HIV with common mental health disorders in Kenya. The investigators will tailor a collaborative care model for peripartum women with HIV experiencing mental health symptoms and evaluate its impact on participants' mental health, antenatal, and HIV care outcomes. The investigators will actively engage key stakeholders throughout the process and assess scalability and sustainability through multi-method approaches. This study will contribute to the overall goal of achieving optimal health outcomes for women living with HIV and their families in sub-Saharan Africa.

Participants needed: 900
Trial details
Age: 15+Biological sex: FemaleType: InterventionalSponsor: University of Colorado, DenverUpdated: May 6, 2026Locations: 1
Eligibility criteria

pregnant woman living with HIV attending an antenatal clinic in southwestern Ken... [+4]

imminent plans of suicide [+1]

Status: Recruiting

Study to Evaluate the Efficacy and Safety of ATNC-MDD V1(TMS With Cognitive Training) in Mild Alzheimer's Dementia

The study tests the effect of the ATNC MDD-V1 on Alzheimer patients' cognitive function. The ATNC MDD-V1 uses non-invasive stimulation of both magnetic and cognitive training.

Participants needed: 180
Trial details
Age: 60-85Biological sex: AllType: InterventionalSponsor: Advanced Technology & CommunicationsUpdated: Apr 23, 2026Locations: 11
Eligibility criteria

Patients who started drug treatment with an acetylcholinesterase inhibitor at le... [+10]

Patients with central nervous system (CNS) disorders that may affect cognitive f... [+20]

Status: Recruiting

Brain Stimulation to the Hippocampus in Schizophrenia

Schizophrenia - marked by delusions, hallucinations, and cognitive deficits - causes the most disability of any mental health condition, but existing treatments have significant side effect burden and are often ineffective. Disordered neural activity in the hippocampus likely contributes to schizophrenia symptoms, but to develop better therapies we need to understand whether hippocampal activity in schizophrenia can be systematically affected by non-invasive brain stimulation techniques like transcranial magnetic stimulation (TMS). This proposal will investigate the use of connectivity-guided theta burst brain stimulation to specifically target hippocampal function in schizophrenia, offering insights into fundamental hippocampal processes, schizophrenia pathophysiology, and potential avenues to use brain stimulation as a therapeutic tool in this devastating illness.

Participants needed: 60
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Stanford UniversityUpdated: Feb 27, 2026Locations: 1
Eligibility criteria

Men and women, ages 18 to 65 years [+4]

DSM5 diagnosis of intellectual disability [+8]

Status: Recruiting

Search for Novel Transcranial Magnetic Stimulation (TMS) Targets for Mental Illness

Participants will receive Transcranial Magnetic Stimulation (TMS) at a random location in the left prefrontal cortex, excluding sites that are potentially unsafe. Extensive behavioral testing will be conducted to determine which behaviors are modulated by stimulating which circuits.

Participants needed: 180
Trial details
Phase: Phase 2Age: 18-65Biological sex: AllType: InterventionalSponsor: Brigham and Women's HospitalUpdated: Feb 17, 2026Locations: 2
Eligibility criteria

Age 18-65 [+8]

Active pregnancy as determined by a urine pregnancy test [+25]

Status: Recruiting

Improving Social Functioning in People With Substance Use and Mental Health Disorders Using VR

ROPVR, a multi-centre, pragmatic randomized controlled trial (RCT) aims to evaluate a VR-technology which has been developed within an exploratory study and a development study, which facilitates social functioning among persons with a substance use and mental health disorder. Investigators will test a VR-program versus treatment as usual among patients enrolled into a long-term addiction-treatment facility. The RCT aims to evaluate the effectiveness of VR training compared to treatment as usual in improving resilience, quality of life, practical and social functioning and social participation (from baseline to 6 months), and to evaluate the cost-effectiveness of VR training versus treatment as usual.

Participants needed: 102
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: Sykehuset Innlandet HFUpdated: Jan 23, 2026Locations: 2
Eligibility criteria

adults aged 18 years or older receiving in-patient SUD treatment in specialized... [+2]

significant visual, auditory, or balance impairment or other diseases affecting... [+2]

Status: Not yet recruiting

Assessment and Evolution of Narrative Identity and Its Relationship to Subjective Multidimensional Well-being and Multidimensional Recovery in First Episode Psychosis

First episode psychosis (FEP) constitutes an important subgroup within psychotic disorders, as the acute impact of a disorder at the time of diagnosis may differ from its long-term impact over the following decades. Narrative is identified as a sense of personal agency, of belonging to a social group, metacognition, and well-being. Patients with schizophrenia have lower levels of agency and communion compared to HIV-positive participants. However, the themes of agency and communion and metacognition do not reflect all factors representing narrative identity. In order to measure well-being, it is also necessary to introduce a specific and multidimensional measure that will allow a more precise understanding of the phenomenon. In FEP, a link has been demonstrated between the specificity of self-recollection and functional outcomes. Given that the transitional developmental stage between adolescence and adulthood is a key developmental window for narrative identity as well as psychotic disorders and that narrative identity is positively associated with mental health, this study will therefore focus on the acquisition of narrative identity in the FEP. It will investigate the extent to which narrative identity has an impact on multidimensional subjective well-being and whether it can predict multidimensional subjective well-being over time. The study investigators hypothesize that the levels of the various components of narrative identity would be lower in cases of FEP compared to patients with other "chronic" psychotic conditions and controls.

Participants needed: 96
Trial details
Age: 16-30Biological sex: AllType: ObservationalSponsor: Centre Hospitalier Universitaire de NīmesUpdated: Jan 9, 2026Locations: 1
Eligibility criteria

Subject who has given their free and informed consent. [+5]

The subject is participating in category 1 RIPH or a clinical drug trial or clin... [+8]

Status: Not yet recruiting

Validation of a VOICE MAnagement Program in Schizophrenia VVoice MAPS

Approximately 25-50% of patients with schizophrenia experience treatment-resistant Auditory Verbal Hallucinations (AVHs), which contribute to the development of associated psychopathological disorders (e.g., anxiety, depression, suicidal ideation). Various validated psychotherapeutic strategies and tools for managing treatment-resistant AVHs have been combined into an integrative therapeutic program. The main objective of this study is to evaluate the efficacy of this program in reducing the frequency and intensity of AVHs, as well as its impact on comorbid psychopathology (e.g., depression, anxiety, self-esteem, substance use) in patients with schizophrenia or schizoaffective disorder who experience treatment-resistant AVHs.

Participants needed: 116
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Centre Hospitalier Universitaire de la GuadeloupeUpdated: Dec 5, 2025Locations: 1
Eligibility criteria

Diagnosis: Fulfill DSM-5 criteria for schizophrenia or schizoaffective disorder. [+4]

Participation in another study: Currently taking part in another clinical trial... [+4]

Status: Recruiting

Going to Altitude With Anxious-depressive Symptoms

Introduction: Currently, there is a lack of international guidelines or clinical recommendations for individuals with mental illnesses (i.e., bipolar disorder, posttraumatic stress disorder) going on high altitude sojourns. However, these guidelines would be important considering that mental illnesses are among the most common disorders worldwide and millions of people are hiking at high altitudes in the Alps, being granted easy access up to 3800m by cable cars. Before conceptualizing these guidelines, it seems necessary to study the physiological and psychological effects of ambient pressure changes leading to oxygen deficiency (hypoxia) in individuals with mental illnesses when being exposed to hypoxic conditions. The investigators hypothesize a shift towards negative affective responses and state anxiety as well as increased levels of neurotransmitter precursor amino acids (PHE/TYR and KYN/TRP) in individuals with mental illnesses when being exposed to hypoxic conditions. Methods and Analysis: The investigators plan to perform a double-blind randomized controlled trial in a safe laboratory environment by using a normobaric hypoxic chamber. Participants suffering from depression and anxiety symptoms will be included as well as age and sex-matched healthy controls. They will attend a six-hour exposure equivalent to 3800m of altitude as well as a six-hour exposure to sham hypoxic conditions. Recruited participants will be screened by the Beck Anxiety and Depression Inventory, the Symptom Checklist (SCL-90) as well as an interview assessment. Affective responses in state anxiety will be assessed before, and during each hour of exposure by using the Feeling Scale (FS), Felt Arousal Scale (FAS), Positive and Negative Affect Schedule (PANAS), State-Anxiety Inventory (STAI) and subjective mental stress levels (Visual Analogue Scale; VAS). Physiological parameters will be assessed by venous blood sampling, pulse oximetry and oxidative stress level measurement before entering the chamber, after three and six hours of exposure. Additionally, symptoms of acute mountain sickness will be assessed by the Lake Louise Score before, after three and six hours of exposure. Follow-up measurements are planned one and seven days after the chamber visit, consisting of venous blood sampling, the Beck Anxiety and Depression Inventory. A series of univariate analyses of covariance (ANCOVA) for repeated measures will be used to test the three-way (i.e. "group × condition × time") and two-way ("group × condition" and "group × time") interactions. Analyses will be adjusted for possible confounding, by adding age, sex, smoking, prior AMS, and medication status in the models as covariates. Ethics and dissemination: Ethical approval has been obtained from the ethics committee of the Medical University of Innsbruck (1250/2021).

Participants needed: 68
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Universitaet InnsbruckUpdated: Dec 10, 2025Locations: 1
Eligibility criteria

sufficient command of the German language [+2]

pregnant or breastfeeding [+3]

Status: Recruiting

Passive Sensor Identification of Digital Biomarkers to Assess Effects of Orally Administered Nicotinamide Riboside

This project's main goal is to use state-of-the-art passive sensing techniques to identify digital biomarkers that relate to bioenergetic changes in the brain due to nicotinamide riboside supplementation in those with mild cognitive impairment and mild Alzheimer's dementia.

Participants needed: 40
Trial details
Age: 18-89Biological sex: AllType: ObservationalSponsor: Mclean HospitalUpdated: Nov 6, 2025Locations: 1
Eligibility criteria

Ability of the participant and/or his/her legally authorized representative to u... [+8]

Current serious or unstable medical or neurological condition that could affect... [+17]

Status: Recruiting

Psychological Outcomes of Strategic Therapy in Adult Outpatients (POST Trial)

This observational study investigates the outcomes of Strategic Psychotherapy, a form of brief psychological treatment focused on specific goals for change, co-constructed with patients. The aim is to evaluate whether patients who receive this therapy in private practice settings experience improvements in their psychological well-being, symptoms, and daily functioning. The study population includes all adult patients (≥18 years) who spontaneously seek treatment from two strategic therapists between January 2021 and December 2025. Eligible participants must present with psychological problems that meet the criteria for a clinical diagnosis. Participants will complete two psychological questionnaires (SCL-90R and CORE-OM) before starting therapy and again at the end of their treatment. Additional information will be collected, such as use of medication, the patient's own evaluation of the therapy, number of sessions attended, initial diagnosis, involvement of family members, and types of prescriptions used. All data will be treated confidentially and used solely for research purposes.

Participants needed: 300
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Società Scientifica di Psicoterapia StrategicaUpdated: Sep 26, 2025Locations: 2
Eligibility criteria

Adults aged 18 years or older. [+3]

Individuals younger than 18 years. [+3]

Status: Recruiting

Healthy ReStart Intervention to Improve Health and Functioning

This study tests an intervention that uses health coaching, motivational interviewing, positive psychology, and online wellness tools to help adults with mental illness return to active lives after major disruptions such as the COVID-19 pandemic.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Illinois at ChicagoUpdated: Sep 15, 2025Locations: 1
Eligibility criteria

Age 18 and older [+4]

A cognitive impairment preventing informed consent [+1]

Status: Recruiting

Pharmacogenomics-Supported Psychotropic Prescribing Trial

Investigate the feasibility and utility of implementing pharmacogenetic testing for adults (aged 18 and older) seeking care for mental illness in Manitoba.

Participants needed: 200
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of ManitobaUpdated: Sep 8, 2025Locations: 2
Eligibility criteria

Aged 18 years or older [+2]

Unwillingness to donate saliva samples for genetic analysis [+3]

Status: Recruiting

GLP-1R Agonist Treatment for Opioid Use Disorder

The goal of this clinical trial is to learn if semaglutide can reduce illicit opioid use in adults in outpatient treatment for opioid use disorder, and who are receiving either buprenorphine or methadone maintenance treatment. The main question it aims to answer is: • Does semaglutide increase the likelihood that participants will refrain from using illicit and nonprescribed opioids? The investigators will compare semaglutide to a placebo (a needle prick that contains no drug) to see if semaglutide works to reduce use of illicit and nonprescribed opioids. The participants will: * Take semaglutide or a placebo every week for 12 weeks * Visit the clinic every week for urine drug screening and pregnancy testing, vital signs, and to complete mental health and drug use questionnaires * Complete smartphone surveys sent at set times during the study

Participants needed: 200
Trial details
Phase: Phase 2Age: 18-75Biological sex: AllType: InterventionalSponsor: Milton S. Hershey Medical CenterUpdated: Aug 14, 2025Locations: 3
Eligibility criteria

Age 18 to 75 years. [+10]

Age < 18 or > 75 years. [+23]

Status: Recruiting

Evaluation of a Digital Pre-therapy Patient Education Program (StartHjelp) in Outpatient Mental Health Care

Community mental health centers (CMHCs) face significant challenges in meeting the needs of individuals with mental health issues. For example, due to high demand, there are long waiting lists and low engagement rates. Innovative interventions are urgently needed to address these challenges to improve patient engagement, coping skills, and overall health outcomes. Educational and self-management interventions have shown promise in enhancing patient activation and treatment satisfaction in other contexts. They may therefore be potential solutions to reduce the identified challenges in the mental health service. To bridge these knowledge and practice gaps, this study aims to evaluate a digital pre-therapy patient education program tailored specifically for adults with mental disorders. This intervention aims to enhance treatment satisfaction, patient activation, knowledge, patient engagement, and overall mental health outcomes.

Participants needed: 170
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: St. Olavs HospitalUpdated: Jun 8, 2025Locations: 1
Eligibility criteria

Put on the waiting list for mental health outpatient treatment in the active stu... [+3]

In need of acute help

Status: Not yet recruiting

Explore the Risk Factors for Antenatal Mental Disorders in Pregnant Women With Hyperglycemia

This study aims to investigate the current situation and risk factors of adverse mental disorders in pregnant women with hyperglycemia. it could include any of the following: 18-45 years old pregnant women with hyperglycemia. The main question is to answer the risk factor for antenatal mental disorder. participants need to complete a self-report questionnaire.

Participants needed: 635
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Shenzhen Hospital of Southern Medical UniversityUpdated: Jun 4, 2025
Eligibility criteria

The pregnant woman was confirmed to have gestational diabetes through biochemica... [+4]

Abnormal fetuses, multiple pregnancies; [+5]

Status: Recruiting

A Transdiagnostic Mentalization-based Intervention for Parents With Mental Disorders

The aim of this randomised clinical trial is to evaluate the short and longterm effects of a transdiagnostic mentalization-based intervention (Lighthouse MBT Parenting Program) compared to care as usal (CAU) for parents with a mental disorder in adult mental health service.

Participants needed: 170
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Mental Health Centre Copenhagen, Bispebjerg and Frederiksberg HospitalUpdated: May 14, 2025Locations: 2
Eligibility criteria

Age >18 years [+5]

Possibility of a learning disability (IQ<75) [+7]

Status: Not yet recruiting

Prevalence of Mental Health Disorders in Junior Anesthetists and Intensivists

Mental health disorders are rapidly growing nowadays and it is well known that people who are subjected to a long term stress are among the highly vulnerable group. Of those, doctors come first specially those working in anesthesia and ICU field owing to the nature of their work where heavy work load, exposure to occupational hazards and competitive environment predominate. More care is needed to identify the magnitude of the ongoing problem and to stand on its determinants to be able to prevent or treat the negative impact on their health and patients as well.

Participants needed: 350
Trial details
Biological sex: AllType: ObservationalSponsor: Ain Shams UniversityUpdated: Apr 30, 2025Locations: 1Duration: 1 Day
Eligibility criteria

working as anesthetist or intensivist [+1]

personality disorders [+1]

Status: Recruiting

Transdiagnostic Behavior Therapy Vs TAU for Adjustment Disorder Following Traumatic Event Exposure

Adjustment Disorder (AjD) is the most common mental health condition diagnosed in Active Duty personnel, and is diagnosed following an extreme stress event such as traumatic loss of a comrade, serious accident or injury, or other intense stress event. Despite its high prevalence, no evidence based treatment for AjD has been subjected to randomized controlled trials. This study seeks to build on the research team's pilot work across several disorders study to benefit service members and Veterans with AjD, a highly prevalent but frequently inadequately treated condition. The investigators will compare the effects of Transdiagnostic Behavior Therapy (TBT) vs treatment as usual which is Moving Forward Problem Solving Therapy (TAU-PST) on AjD symptom outcomes. The investigators hypothesize that TBT will result in greater overall symptom reduction compared to TAU-PST.

Participants needed: 150
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: The University of Texas Health Science Center, HoustonUpdated: Dec 6, 2024Locations: 1
Eligibility criteria

Adult male or female over the age of 18 that has served, or is currently serving... [+2]

Active psychosis [+2]

Status: Recruiting

Dexmedetomidine and Magnesium Sulfate in the Reduction Cognitive Dysfunction in Geriatrics

Magnesium sulfate is considered a neuroprotective drug and has been studied in various applications. Recently, it has drawn the attention of anesthesiologists, resulting in numerous publications about its role in anesthesiology. Magnesium sulfate is suggested to exert its neuroprotective effect by preventing excitotoxicity. in the clinical setting, intraoperative magnesium sulfate attenuated POCD. Furthermore, postoperative emergence agitation was significantly reduced in pediatric patients who received intraoperative magnesium sulfate during adenotonsillectomy. The aim of this study The aim of this work is to compare the protective effect of intraoperative dexmedetomidine with magnesium sulfate against developing POCD and to study their effect on serum level of CRP; the marker of neuronal degeneration.

Participants needed: 58
Trial details
Phase: Phase 1Age: 60-80Biological sex: AllType: InterventionalSponsor: Fayoum UniversityUpdated: Nov 25, 2024Locations: 1
Eligibility criteria

ASA physical status I, II and ⅠⅠⅠ [+1]

Elderly patients with preoperative MoCA Score below 26. [+2]

Status: Recruiting

The VIA Family 2.0 - a Family Based Intervention for Families with Parental Mental Illness

VIA Family 2.0 - a Family Based Intervention for families with parental mental illness Background: Children born to parents with mental illness have consistently been shown to have increased risks for a range of negative life outcomes including increased frequencies of mental disorders, somatic disorders, poorer cognitive functioning, social, emotional and behavioral problems and lower quality of life. Further these children are often overlooked by both society and mental health services, although they represent a potential for prevention and early intervention. A collaboration between researchers and clinicians from two regions, the Capital Region and the North Region Denmark has been established as the Research Center for Family Based Interventions. The research center is an umbrella for a series of research activities, all focusing on children and adolescents in families with parental mental illness. Method: A large randomized, controlled trial (RCT) for families with parental mental illness will be conducted in order to evaluate the effect of a two-year multidisciplinary, holistic team intervention (the VIA Family 2.0 team intervention) against treatment as usual (TAU). Inclusion criteria will be biological children 0-17 of parents with any mental disorder treated in the secondary sector at any time of their life and receiving treatment in primary or secondary sector within the previous three years. A total of 870 children or approx. 600 families will be included from two sites. Primary outcomes will be changes in child well being, parental stress, family functioning and quality of the home environment, . Time plan: The RCT will start including families from March 1st, 2024 to Dec 2025 (or later if needed). All families will be assessed at baseline and at end of treatment, i.e. after 24 months and after 36 months. Baseline data will inform the intervention team about each family's needs, problems, and motivation. TAU will be similar in the two regions, which means three family meetings and option for children to participate in peer groups. Challenges: final funding is being applied for. Recruitment of families can be challenging but we have decades of experience in conducting research in the field. Since both the target group, their potential problems and the intervention is complex, primary outcome is difficult to determine.

Participants needed: 1,452
Trial details
Age: 0-17Biological sex: AllType: InterventionalSponsor: Mental Health Centre Copenhagen, Bispebjerg and Frederiksberg HospitalUpdated: Oct 26, 2024Locations: 1
Eligibility criteria

At least one of the parents must be living in Capital Region or in Region North,... [+3]

Not fulfilling inclusion criteria [+5]

Status: Recruiting

Evaluation of the Supported Housing System for the Inclusion of People Suffering From Mental Disorders

Access to housing, in the current context of extreme tension in the rental housing market in Paris and throughout the Ile-de-France region, is proving to be extremely complex for people with mental health problems.National and international scientific studies have quantified the problem of homelessness and precarious or inappropriate housing among patients suffering from psychiatric disorders, and show the impact of housing problems on the consumption of psychiatric care.The DÉLAI's mission is to facilitate access to housing for people enrolled in a psychiatric care pathway, with teams from the psychiatric sectors

Participants needed: 50
Trial details
Age: 18-60Biological sex: AllType: InterventionalSponsor: Centre Hospitalier St AnneUpdated: Oct 10, 2024Locations: 1
Eligibility criteria

Not listed