Depression, Anxiety

63

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

Condition / disease
Location
Status: Recruiting

Technology-assisted Methods to Advance Suicide Prevention Among Youth in Colombia

This study will investigate a multi-level approach that applies technology-assisted methods to reduce suicidal thoughts and behaviors (SIB) and promote mental health among Colombian youth: (a) digital platform for youth; (b) digital platform for teachers; and (c) hybrid mental health training diploma program for teachers. This approach will evaluate an open-access digital platform for suicide prevention among Colombian youth. Key features of the digital platform include mental health self-help tools, a customizable safety plan, links to online counseling services, and gamification elements. The digital platform's teacher interface will incorporate psychoeducation, brief suicide-risk screening and decision support tools to enhance teacher capacity to assess risk for suicide and refer youth to the appropriate level of services. Study investigators will conduct a hybrid-type 1 implementation-effectiveness stepped wedge pilot trial design to evaluate the digital platform and hybrid mental health teacher training program implemented within secondary schools in Bogota, Colombia. Study aims are to: Aim 1. An initial needs assessment will be conducted with key stakeholders (youth, teachers, caregivers, school administrators) to identify barriers and facilitators to successful implementation of the multi-level approach. User-centered design methods will be used to refine the digital platform and incorporate end-user feedback into the final prototype. Aim 2. Investigators will evaluate: (a) feasibility, acceptability, and usability of the digital platform across three schools in Colombia; and (b) the preliminary effects of the digital platform in reducing SIB and improving mood (e.g., anxiety/depression) among Colombian youth aged 14-19 attending the three schools. Safety planning skills acquisition (youth-level) and linkages to mental health services (service-level) will be assessed as potential mechanisms of change. Aim 3. The study will apply a multi-disciplinary capacity building model to strengthen behavioral health and implementation science research, healthcare delivery capacity, and mental health policy. In partnership with Pontificia Javeriana University, experts in suicide prevention, data science, and implementation science will be engaged to build in-country research capacity at the individual and institutional level.

Participants needed: 228
Trial details
Age: 14-19Biological sex: AllType: InterventionalSponsor: Brown UniversityUpdated: Jul 13, 2026Locations: 1
Eligibility criteria

aged 14-19 [+2]

not meeting inclusion criteria

Status: Recruiting

Psilocybin-Assisted Psychotherapy in Patients With Advanced Cancer on Maintenance Therapy

To learn about the feasibility, safety, and effects of psilocybin-assisted psychotherapy on depression and/or anxiety in participants who are being treated for advanced cancer.

Participants needed: 30
Trial details
Phase: Phase 2Age: 25+Biological sex: AllType: InterventionalSponsor: M.D. Anderson Cancer CenterUpdated: Jun 24, 2026Locations: 1
Eligibility criteria

Participants must have one of the following histology documented tumor types: no... [+14]

History of depression prior to cancer diagnosis. [+16]

Status: Recruiting

Efficacy and Safety of Magnesium Vitamin B6 in First Episode Bipolar Disorder

This is a randomized, double-blind, placebo-controlled proof-of-concept clinical trial to assess the efficacy and safety of Magnesium-vitamin B6in combination with treatment as usual for treating symptoms of depression, stress, and anxiety in patients with first episode bipolar I disorder.

Participants needed: 40
Trial details
Phase: Phase 2Age: 18-50Biological sex: AllType: InterventionalSponsor: Mclean HospitalUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Persons between the ages of 18 and 50 [+5]

Unable to sign informed consent. [+21]

Status: Recruiting

Multidimensional Sleep Health Intervention to Optimize Concussion Recovery

Following adolescent concussion, poor sleep health is common and relates to the development of persisting post-concussion symptoms, and uninjured adolescents (independent of concussion) also commonly experience sleep insufficiency. Given the sparse guidance that exists for clinicians to provide evidence-based sleep health recommendations for adolescents with a concussion, the primary objectives of this prospective randomized clinical trial of adolescents with a recent concussion are to discover if a multidimensional and prescriptive sleep health intervention leads to: 1) faster symptom resolution time, better sleep quality, or longer sleep duration; and 2) improved sleep habits, mental health, or academic engagement, relative to standard-of-care post-concussion sleep health guidance. Findings from this research will provide the basis for more precise sleep health recommendations for adolescents who experience a concussion.

Participants needed: 54
Trial details
Age: 10-19Biological sex: AllType: InterventionalSponsor: University of Colorado, DenverUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

Participants will be symptomatic at the time of enrollment (Post-Concussion Symp... [+2]

History of treatment for pre-concussion sleep-related disorders

Status: Recruiting

Internet-Delivered Cognitive Behaviour Therapy for Public Safety Personnel

This study evaluates a transdiagnostic Internet-delivered cognitive behavioural therapy (ICBT) recently tailored for Canadian public safety personnel (PSP) reporting symptoms of depression, anxiety, or posttraumatic stress. Outcomes of interest include engagement with the intervention, changes in symptoms and functioning, and strengths and limitations of implementing ICBT with Canadian PSP.

Participants needed: 250
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of ReginaUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

18 years of age or older [+4]

high suicide risk [+5]

Status: Recruiting

Training in Evidence-based Treatments in Psycho-Oncology

The goal of this research study is to train psychotherapists to administer individualized evidence-based psychotherapies in a cancer care setting to patients and caregivers with elevated levels of distress. The intervention will mirror clinical care in psycho-oncology in which the therapist, collaboratively with their supervisor, will choose specific components of the following evidence-based treatments to administer based on the clinical presentation of the patient or caregiver and referring problem. * Cognitive Behavioral Therapy (CBT) * Acceptance Commitment Therapy (ACT) * Mindfulness-Based Cognitive Therapy (MBCT) * Mindfulness-Based Stress Reduction (MBSR) * Meaning-Centered Psychotherapy (MCP) * Cognitive Behavioral Therapy for Insomnia (CBT-I) * CBT for other cancer-related physical symptoms like pain, fatigue, and nausea. Participation in this research study is expected to last about 26 weeks. It is expected that about 75 patients, 25 caregivers, and 15 therapists will take part in this research study.

Participants needed: 115
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Massachusetts General HospitalUpdated: Jun 15, 2026Locations: 1
Eligibility criteria

Adults > 18 years of age. [+11]

Has uncontrolled psychosis, active suicidal ideation, or psychiatric hospitaliza... [+3]

Status: Recruiting

Test of Target Engagement of Ambiguity Aversion

The present work aims to test whether a single session intervention alters ambiguity aversion, both in terms of people's decision making and their brain responses to ambiguous choices.

Participants needed: 140
Trial details
Age: 25-60Biological sex: AllType: InterventionalSponsor: Northwestern UniversityUpdated: May 26, 2026Locations: 1
Eligibility criteria

Ages 25 to 60 [+4]

Personal history of psychosis, mania, or hypomania [+6]

Status: Recruiting

Harlem Strong Mental Health Coalition

Addressing health disparities, especially in the face of coronavirus pandemic, requires an integrated multi-sector equity-focused, community-based approach. This study will examine the impact of Harlem Strong Community Mental Health Collaborative, a community-wide multi-sectoral coalition in which a health insurer works with a network of community-based organizations, medical providers, and behavioral health providers to engage in a network-wide implementation planning process to: (1) problem-solve financing, access, and quality of care barriers, (2) support capacity building for mental health (MH) task-sharing for community health workers, (3) facilitate coordination and collaboration across MH/behavioral health, primary care, and a range of social services, including case management, housing supports, financial education, employment support, and other community resources to improve linkages to services, and (4) identify a set of common MH, social risk, and health metrics and strategies to integrate these metrics into data systems across the network for continuous quality improvement of the system. The long-term goal of our study is to develop sustainable model for task-sharing MH care that will be embedded in a coordinated comprehensive network of services, including primary care, behavioral/MH, social services, and other community resources.

Participants needed: 700
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: City University of New York, School of Public HealthUpdated: May 20, 2026Locations: 2
Eligibility criteria

Black and Latino adults between 18 and 65 years [+2]

Those with risk for depression or anxiety who screen positive for severe mental...

Status: Recruiting

The COMParing App Support Strategies Study

The overall purpose of this study is to help determine how best to incorporate small amounts of human and digital support into a meditation app. The meditation app used is the Healthy Minds Program (HMP) which provides training in four pillars of well-being (Awareness, Connection, Insight, Purpose) through a combination of podcast-style didactic material and guided meditation practices.

Participants needed: 688
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: University of Wisconsin, MadisonUpdated: May 18, 2026Locations: 1
Eligibility criteria

Elevated symptoms of depression and/or anxiety (PHQ-9 greater than or equal to 1... [+3]

Non-US citizen or legal resident (green card holder) [+4]

Status: Recruiting

Youth Emotional and Behavioral Treatment Study

This study aims to characterize key mechanisms underlying the development, maintenance, and treatment of severe irritability in a clinically heterogeneous sample of school-aged youth.

Participants needed: 500
Trial details
Age: 4-17Biological sex: AllType: InterventionalSponsor: Florida State UniversityUpdated: May 14, 2026Locations: 1
Eligibility criteria

Children between the ages of 4-17 years [+3]

Gross neurological, sensory, or motor impairment [+3]

Status: Recruiting

Prevention of Psychological Health Problems Via Integrated Operational Support

Sub-clinical behavioral health services in the military are performed by BH technicians, who receive minimal training. Due to this, embedding more technicians in military units is unlikely to benefit service members. Giving technicians training in, and access to, evidence-based interventions (EBI) could make their work more effective. The proposed study is a training trial examining the efficacy of the full integrated operational support (IOS) toolkit (evidence-based interventions for behavioral health), relative to routine care using standard resources, as a prevention resource for active-duty airmen.

Participants needed: 5,586
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: New York UniversityUpdated: May 15, 2026Locations: 1
Eligibility criteria

Service members seeing a behavioral health (BH) technician. [+1]

Service members who are not currently seeing a BH technician. [+1]

Status: Recruiting

Modulating Exercise Dosage to Improve Concussion Recovery

Aerobic exercise has emerged as an effective treatment to reduce sport-related concussion symptom severity, yet existing work lacks rigor regarding the precise exercise volume and intensity required to elicit therapeutic effects, how exercise can alter concussion-related pathophysiology, and whether exercise can prevent the development of secondary sequelae. Our objective is to examine if a high dose exercise program (higher volume than currently prescribed at an individualized, safe intensity level) initiated within 14 days of concussion results in faster symptom resolution, altered physiological function, or reduced secondary sequalae. Findings from this research will lead to more rigorous and precise rehabilitation guidelines and improved understanding about how exercise affects neurophysiological function among adolescents with concussion.

Participants needed: 216
Trial details
Phase: Phase 2Age: 13-18Biological sex: AllType: InterventionalSponsor: University of Colorado, DenverUpdated: May 6, 2026Locations: 3
Eligibility criteria

13-18 years of age [+2]

Pre-existing neurological disorders [+2]

Status: Recruiting

Acceptance and Commitment Therapy for Adolescents and Young Adults With Sickle Cell Disease

The current study seeks to build on previous research that demonstrates the efficacy of Acceptance and Commitment Therapy in combating stigma by investigating the feasibility and acceptability of a protocol to support Black adolescents and young adults in coping with race related stress. The study will consist of a small, purposeful, non-randomized sample (N = 30) of clients enrolled into a 10-session Acceptance and Commitment Therapy group. The group will be offered as part of regular clinical care at the Division of Adolescent and Young Adult Medicine. Three consecutive groups will be run with approximately 8-10 participants in each group over the next year.

Participants needed: 66
Trial details
Phase: Phase 1, Phase 2Age: 14-21Biological sex: AllType: InterventionalSponsor: Children's Hospital Los AngelesUpdated: May 6, 2026Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Just-In-Time Adaptive Interventions (JITAIs) in a Digital Mental Health Intervention for Middle-Aged and Older Adults With Chronic Pain

The purpose of this research study is to refine customized in-app notifications in order to optimize users' experience with a mobile app called Wysa for Chronic Pain. This app is designed to support people who have chronic pain and who also experience symptoms of depression and/or anxiety. This version of the app is not currently available to the public. Eligible participants will be asked to download and use the Wysa for Chronic Pain study app for several weeks, and to use it as they normally would if they were not part of a research study. At the beginning and end of the study period, participants will be asked to complete brief surveys about their mood, pain, physical function, and sleep. Additionally, a few participants will be asked to share their experience with the study app at the end of the research study in a casual interview using a secure audio/video recorded call. Participating in the interview portion is optional.

Participants needed: 1,000
Trial details
Age: 45+Biological sex: AllType: InterventionalSponsor: Washington University School of MedicineUpdated: May 5, 2026Locations: 1
Eligibility criteria

45 years or older [+2]

Frequent active suicidal ideation [+2]

Status: Recruiting

Pilot Effectiveness Trial of an ACT Self-help Workbook Tailored Specifically for Prisons

The goal of this research study is to adapt an ACT-self-help workbook to the prison setting and determine the feasibility acceptability, and effectiveness of this workbook. Participants can expect to be in the study for 13 weeks.

Participants needed: 96
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: University of Wisconsin, MadisonUpdated: May 4, 2026Locations: 1
Eligibility criteria

18 years of age or older [+5]

Unable to provide informed consent [+2]

Status: Not yet recruiting

Online Intervention for Transgender/Nonbinary Young Adults' Experiences With Alcohol and Romantic Relationships

The objective of this study is to learn more about Whole Selves, an interactive online resource ("intervention") to help transgender and/or nonbinary young adults reflect on their experiences and goals related to both alcohol use and romantic relationships. Existing online interventions focused on alcohol use often aren't a good fit for trans/nonbinary people, and existing relationship education programs don't account for how being trans/nonbinary might influence someone's relationships. For these reasons, the investigator is working with trans/nonbinary young adults and other community stakeholders to create a new intervention specifically for trans/nonbinary young adults. The goals of this clinical trial are to: 1. Find out what transgender/nonbinary young adults think of the Whole Selves intervention in order to improve it 2. See whether the Whole Selves intervention seems to work as expected 3. Help the investigator make plans for a bigger clinical trial of the Whole Selves intervention, which could tell us how well it works In this study, participants will use the Whole Selves intervention; complete online surveys about themselves, their romantic relationship experiences, their mental health, their alcohol use; and provide feedback on the Whole Selves intervention.

Participants needed: 107
Trial details
Age: 18-30Biological sex: AllType: InterventionalSponsor: Boston UniversityUpdated: Apr 28, 2026Locations: 1
Eligibility criteria

Self-identify as transgender and/or nonbinary [+4]

Prospective participants will be excluded as potentially inauthentic (i.e., not...

Status: Recruiting

Weekly Dynamics of Psychopathological and Symptom Networks During Mindfulness-Based Interventions for Emotional Distress

The goal of this clinical study is to learn how Mindfulness Intervention for Emotional Distress (MIED) helps people with emotional distress and how their symptoms and psychological patterns change over time. The main questions it aims to answer are: * How do the relationships between emotions, thoughts, and behaviors change week by week during mindfulness training? * Which psychological skills, such as distress tolerance or cognitive flexibility, improve first and lead to later emotional relief? Two groups will be compared - one that takes part in an online mindfulness intervention and one that waits to join - to see how the intervention changes emotional and psychological networks over time. Participants will: * Complete a 7-week online self-guided Mindfulness Intervention for Emotional Distress(iMIED) designed for people experiencing high emotional distress. * Fill out short weekly questionnaires about their emotions, thoughts, and behaviors before, during, and after the course (9 times in total). * Receive access to the mindfulness program after the study if they are in the wait-list group. This study includes about 500 adults aged 18 and older who feel anxious, depressed, or emotionally distressed but have no major psychiatric disorders. By tracking weekly changes, the research aims to identify how mindfulness intervention leads to emotional improvement and which skills play the most important roles in that process.

Participants needed: 500
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Peking UniversityUpdated: Apr 27, 2026Locations: 1
Eligibility criteria

experiencing emotional distress such as depression or anxiety (Kessler-10 score...

prior experience with mindfulness meditation [+4]

Status: Recruiting

Promoting Mental Health of Teachers and Caregiver Using a Personalized mHealth Toolkit in Uganda

This study record describes a two-phase of clinical trial study. The first phase is a pilot study phase (to study feasibility and efficacy of the intervention), and the second phase is an effectiveness study phase (a fully powered evaluation study to test the intervention effectiveness). This proposal seeks to develop and test a new mHealth intervention, the mHealth Toolkit for Wellness \& Empowering Lives of School Community (mWEL) in Uganda. The mWEL-digial toolkit is a preventive intervention tool for teachers and parents as a self-help support modality. Caregivers who need support in navigating the toolkit will be supported by peer-community health workers (P-CHWs).

Participants needed: 1,180
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: NYU Langone HealthUpdated: Apr 20, 2026Locations: 2
Eligibility criteria

Teaching in recruited schools. [+3]

Evidence of psychopathology or cognitive impairment severe enough to preclude gi... [+3]

Status: Recruiting

Adaptation of an Intervention Addressing Barriers to PrEP Use Among Pregnant Women in Zimbabwe

The purpose of this study is to develop a multi-level PrEP adherence and persistence intervention as an adaptation of the TENDAI ('grateful' in Shona) program, a problem-solving approach to reduce depression and increase HIV treatment adherence among people living with HIV in Zimbabwe. The new intervention, TENDAI4PrEP, will be designed to improve PrEP uptake and persistence among pregnant persons in Zimbabwe. If feasibility, acceptability, and preliminary efficacy are demonstrated, the intervention will be ready for large-scale effectiveness/implementation testing. This program will has the potential to address a critical public health challenge impacting pregnant and postpartum persons in Zimbabwe: the prevention of HIV acquisition and transmission.

Participants needed: 132
Trial details
Age: 15-55Biological sex: AllType: InterventionalSponsor: Massachusetts General HospitalUpdated: Mar 31, 2026Locations: 1
Eligibility criteria

Pregnant [+8]

Inability to provide informed consent/assent and/or complete procedures in Shona... [+1]

Status: Recruiting

Validation of a Rapid Screening Tool for Anxiety-depressive Disorders in Children, Adolescents and Young Adults Treated in Oncology. Multicenter Study.

In France today, it is estimated that one in every 850 people aged between 20 and 45 is a childhood cancer survivor (CCS), equivalent to around 40,000 to 50,000 people. Some descriptive studies have established that the diagnosis and treatment of cancer can affect psychological health. A French study published by our team in 2015 and 2020 showed that in adulthood, 40% of CCS had anxiety symptoms, a rate significantly higher than that of the general French population (25%). However, although there are validated scales for screening children for psychological disorders (anxiety, depression, etc.), there is no rapid screening tool that can be used routinely by an oncologist during consultations. So, the study aims to develop and validate a short test, which could easily be carried out systematically during follow-up consultations after childhood cancer. It would make it possible to identify people with no psychological complications and, conversely, those in whom further investigation, based on the classic reference scales for assessing psychological disorders, would be relevant.

Participants needed: 545
Trial details
Age: 7-25Biological sex: AllType: ObservationalSponsor: Centre Hospitalier Universitaire de Saint EtienneUpdated: Mar 30, 2026Locations: 7
Eligibility criteria

Patients diagnosed with pediatric cancer before the age of 18, [+4]

Refusal to participate expressed by the patient or minor, [+4]

Status: Recruiting

intErnet-based iNterventions FOR Cardiac arrEst suRvivors

This randomized clinical trial will test whether an internet-based lifestyle intervention administered through a web app can foster Health Related Quality of Life in patients who survived an out-of-hospital cardiac arrest and suffer from these symptoms

Participants needed: 106
Trial details
Age: 18-80Biological sex: AllType: InterventionalSponsor: Azienda Usl di BolognaUpdated: Mar 30, 2026Locations: 2
Eligibility criteria

Hospital discharge after out-of-hospital cardiac arrest with Cerebral Performanc... [+3]

Previous cognitive dysfunction [+2]

Status: Recruiting

Technology-assisted Methods to Advance Suicide Prevention Among Youth in Colombia

This study will investigate a multi-level approach that applies technology-assisted methods to reduce suicidal thoughts and behaviors (SIB) and promote mental health among Colombian youth: (a) digital platform for youth; (b) digital platform for teachers; and (c) hybrid mental health training diploma program for teachers. This approach will evaluate an open-access digital platform for suicide prevention among Colombian youth. Key features of the digital platform include mental health self-help tools, a customizable safety plan, links to online counseling services, and gamification elements. The digital platform's teacher interface will incorporate psychoeducation, brief suicide-risk screening and decision support tools to enhance teacher capacity to assess risk for suicide and refer youth to the appropriate level of services. Study investigators will conduct a hybrid-type 1 implementation-effectiveness stepped wedge pilot trial design to evaluate the digital platform and hybrid mental health teacher training program implemented within secondary schools in Bogota, Colombia. Study aims are to: Aim 1. An initial needs assessment will be conducted with key stakeholders (youth, teachers, caregivers, school administrators) to identify barriers and facilitators to successful implementation of the multi-level approach. User-centered design methods will be used to refine the digital platform and incorporate end-user feedback into the final prototype. Aim 2. Investigators will evaluate: (a) feasibility, acceptability, and usability of the digital platform across three schools in Colombia; and (b) the preliminary effects of the digital platform in reducing SIB and improving mood (e.g., anxiety/depression) among Colombian youth aged 14-19 attending the three schools. Safety planning skills acquisition (youth-level) and linkages to mental health services (service-level) will be assessed as potential mechanisms of change. Aim 3. The study will apply a multi-disciplinary capacity building model to strengthen behavioral health and implementation science research, healthcare delivery capacity, and mental health policy. In partnership with Pontificia Javeriana University, experts in suicide prevention, data science, and implementation science will be engaged to build in-country research capacity at the individual and institutional level.

Participants needed: 228
Trial details
Age: 14-19Biological sex: AllType: InterventionalSponsor: Brown UniversityUpdated: Mar 23, 2026Locations: 1
Eligibility criteria

aged 14-19 [+2]

not meeting inclusion criteria

Status: Not yet recruiting

ACT-based Parenting Program for Caregivers of Children With Hearing Loss Post-cochlear: A Pilot Randomised Controlled Trial

The purpose of the proposed pilot randomized controlled design study is to evaluate the feasibility, acceptability, and potential effectiveness of using a videoconferencing-based individual Acceptance and Commitment Therapy (ACT) approach to enhance the mental well-being and parenting competence of parents of children with hearing loss post-cochlear implantation over a three-month period after the intervention has taken place.

Participants needed: 64
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Second Xiangya Hospital of Central South UniversityUpdated: Mar 17, 2026
Eligibility criteria

Mandarin-speaking Chinese residents aged ≥18 years. [+4]

Parents with cognitive deficiency, severe mental illness and/or disability condi... [+3]

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: Not yet recruiting

Managing Hepatitis B (Hep. B) and Human Papilloma Virus (HPV) Related Cancers and Mental Health.

Aim: The main goal of this observational study is to determine the prevalence of Human Papilloma Virus(HPV) infection, and Hepatitis B (Hep B) immunity amongst women of childbearing age 13 to 45 years) attending clinics at Mtshabezi Mission and Matobo clinic respectively; and assess behavioral risk factors of high school students at these catchment areas that can put them at risk for developing cancer of the cervix and liver. Question: Can screening for cancer, and vaccination against Hep B and HPV, and cognitive behavior intervention help in preventing related cancers amongst these groups of participants.

Participants needed: 1,800
Trial details
Phase: Phase 4Age: 13-45Biological sex: AllType: InterventionalSponsor: Eunice DubeUpdated: Jan 21, 2026
Eligibility criteria

males who are not enrolled in these participating High Schools. [+3]