Adolescents

13

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

Condition / disease
Location
Status: Recruiting

A Prospective, Single-arm Clinical Study of Liposomal Mitoxantrone Combination Regimen in the Treatment of Relapsed and Refractory Solid Tumors in Children, Adolescents and Young Adults

The aim of this clinical study is to determine the efficacy and safety of the liposomal mitoxantrone combination regimen in treating relapsed and refractory solid tumors among children, adolescents, and young adults. The key questions it intends to address are: Can the liposomal mitoxantrone combination regimen improve the objective response rate (ORR) compared to historical data? What are the adverse events associated with this combination regimen? Researchers will administer the liposomal mitoxantrone combination regimen (including capecitabine and anlotinib with specific dosing regimens) to the participants and closely monitor their conditions. Participants will: Receive the treatment regimen for 4 - 6 cycles, with each cycle lasting 21 days Undergo regular checkups and tests during the treatment period and follow-up period as per the protocol. Have their tumor status, blood parameters, and other relevant indicators measured to evaluate the treatment effect and safety.

Participants needed: 49
Trial details
Phase: Phase 2Age: 6-24Biological sex: AllType: InterventionalSponsor: Cancer Institute and Hospital, Chinese Academy of Medical SciencesUpdated: May 7, 2026Locations: 1
Eligibility criteria

The patient fully understands this study, voluntarily participates and signs the... [+7]

Patients with known hypersensitivity to any component of the study drugs. [+3]

Status: Recruiting

Child Bipolar Network Ketogenic Diet Approach to Bipolar Disorder in Adolescents

The present study is an open trial of ketogenic diets for adolescents and young adults (ages 12-21 yrs) in the depressive or mixed phases of bipolar disorder (BD). The investigators aim to determine whether combining standard of care pharmacological treatment for bipolar spectrum disorders with a 16-week ketogenic diet is well-tolerated and associated with improvements in depression, inflammatory and metabolic indicators, and executive functioning over the study period. The experimental treatment in this study is a 16-week full ketogenic diet. Four study sites (UCLA, U Cincinnati, U Colorado and U Pittsburgh) will recruit 80 total youth (20 each) from bipolar specialty clinics. All youth eligible for the ketogenic therapy will be provided with the ketogenic diet and standard of care pharmacological treatment. During the diet therapy youth will be seen by a study child/adolescent psychiatrist at least once a month (and more frequently when needed), with the psychiatrist recommending and providing side effects monitoring and pharmacotherapy as clinically indicated. The youth and caregivers will also meet with an expert dietitian who will coach all youth on maintaining the ketogenic diet (low carbs, high fats, medium protein) and making sure the child is tolerating the diet and getting enough liquid and nutrients, following the practice guidelines of the International Ketogenic Diet Study Group for treating youth. All youth and involved caregivers will also be provided will at least one motivational enhancement session to support them in goal setting and completion of the study elements. Throughout the study the investigators will assess metabolic (e.g., blood ketones, HOMA-IR) and inflammatory indicators (e.g., C-reactive protein), both for safety reasons and to assess correlates of symptomatic change. Independent evaluators will assess youth every month regarding their symptoms (depression, mania, anxiety, psychosis), psychosocial functioning, and quality of life. The investigators anticipate that the pilot will transpire over 24 months and be an important step toward establishing feasibility and acceptability of ketogenic therapy for this population, not only in terms of diet administration and compliance but also for obtaining symptomatic, metabolic and inflammatory measurements.

Participants needed: 80
Trial details
Age: 12-21Biological sex: AllType: InterventionalSponsor: University of California, Los AngelesUpdated: Apr 22, 2026Locations: 4
Eligibility criteria

Youth must be ages 12 to 21 years old and speak English [+7]

pregnancy or breastfeeding [+17]

Status: Not yet recruiting

Effect of Core Stabilization Exercises Versus Traditional Rehabilitation in Adolescent With Idiopathic Scoliosis

This study aims to compare the effectiveness of core stabilization exercises versus traditional rehabilitation exercises in adolescents with idiopathic scoliosis. Participants are assigned to one of two intervention groups: a core stabilization exercise program or a traditional rehabilitation program. The study evaluates the impact of both interventions on spinal stability, posture, and functional outcomes. The results of this study may help identify more effective rehabilitation approaches for managing adolescent idiopathic scoliosis.

Participants needed: 60
Trial details
Age: 11-18Biological sex: FemaleType: InterventionalSponsor: Armed Forces Hospitals, Southern Region, Saudi ArabiaUpdated: Jan 27, 2026Locations: 1
Eligibility criteria

Female adolescents aged 11-18 years [+3]

Congenital, neuromuscular, or secondary scoliosis [+3]

Status: Recruiting

Omega-3 Fatty Acids, Neuroendocrine and Attention Deficit Hyperactivity Disorder (OMNeADHD)

This is a 12 week randomized controlled study on the effects of omega-3 fatty acids in youth with attention deficit hyperactivity disorder (ADHD) with omega-3 deficiency.

Participants needed: 100
Trial details
Age: 6-18Biological sex: AllType: InterventionalSponsor: China Medical University HospitalUpdated: Jan 26, 2026Locations: 1
Eligibility criteria

DSM-5 diagnosis of ADHD [+2]

IQ<80 [+3]

Status: Recruiting

Digital Phenotyping for Psychosocial Screening in Adolescents and Young Adults With Cancer

The overall goal of the proposed study is to use digital phenotyping to identify and triage at-risk patients and accelerate access to critical mental health services.

Participants needed: 25
Trial details
Age: 10-25Biological sex: AllType: InterventionalSponsor: Stanford UniversityUpdated: Dec 30, 2025Locations: 1
Eligibility criteria

10-25 years old [+3]

Significant physical or mental disability that prevents completion of study acti... [+1]

Status: Recruiting

Evaluation of Trauma Center-Based Intervention for Adolescent Traumatic Injury Survivors

Pediatric traumatic injury (i.e., injury of sudden onset and severity requiring immediate attention) is the leading cause of death and morbidity among US adolescents and are associated with mental health and health risk outcomes, including posttraumatic stress and depression (affecting between 19-42%), deficits in physical recovery, social functioning and quality of life, which if unaddressed, may contribute to increased use of health care services. The investigators partnered with three accredited Level I and II pediatric trauma centers to conduct a multi-site hybrid 1 effectiveness-implementation trial with 300 adolescent (ages 12-17) traumatic injury patients to assess the extent to which the Trauma Resilience and Recovery Program (TRRP), a scalable and sustainable, technology-enhanced, multidisciplinary stepped model of care, promotes improvement in quality of life and emotional recovery and gather preliminary data on the potential for TRRP to be implemented in other Level I trauma centers. Directly in line with NICHD's Pediatric Trauma and Critical Illness Research and Training (PTCIB) Strategic Research and Training agenda, this study will provide valuable data on the efficacy, preliminary effectiveness and potential for implementation of an innovative, cost-effective, sustainable technology-enhanced intervention designed to address the unique needs of adolescent injury patients and mitigate short- and long-term impact of injury on mental health, quality of life, and overall well-being.

Participants needed: 300
Trial details
Age: 12-17Biological sex: AllType: InterventionalSponsor: Medical University of South CarolinaUpdated: Aug 11, 2025Locations: 1
Eligibility criteria

adolescent ages 12-17 admitted following traumatic injury [+1]

if the injury was self-inflicted [+1]

Status: Recruiting

Peanut Consumption on Cognitive, Weight, and Inflammation

A multi-school, two-arm parallel cluster-randomized controlled trial will be conducted in 200 healthy young adolescents from Barcelona (Spain) to evaluate the effect of peanut consumption on cognitive performance, weight management and inflammation. Schools willing to participate will be randomly assigned to either the intervention or the control group. After the recruitment, the participants will follow a peanut-free diet for two weeks. Both arms will receive a multidimensional educational intervention designed by the Gasol Foundation to promote healthy dietary habits based on Mediterranean diet recommendations, along with exercise performance, healthy sleeping habits and emotional knowledge. Half of the participants (intervention group) will consume 25 g of whole skin roasted peanuts as a daily snack to be incorporated into their diet for six months.

Participants needed: 200
Trial details
Age: 10-12Biological sex: AllType: InterventionalSponsor: University of BarcelonaUpdated: Apr 3, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Integration to Improve Adolescent Health and HPV Vaccination in Laos

The goal of this study is to find out if adding HPV vaccination to adolescent health services works to increase HPV vaccine uptake in 10-13-year-old girls in Laos. The study will also look at the effects of adding HPV vaccination on the use of other health services in 10-13-year-old boys and girls. The main questions the study aims to answer are: 1. Does adding HPV vaccination to adolescent health services increase HPV vaccine uptake in girls aged 10-13 years compared to girls who only receive standard HPV vaccination services? 2. Does adding HPV vaccination to adolescent health services increase the use of other health services in 10-13-year-old adolescent boys and girls compared to adolescents who only receive standard HPV vaccination services? 3. What are the barriers and facilitators to using the combined intervention in Laos? 4. What are the opinions of adolescents, caregivers, healthcare providers, and other stakeholders on the combined intervention? 5. How much does it cost and how well it works to combine HPV vaccination with adolescent health services, as opposed to providing HPV vaccination alone? Researchers will compare a combined intervention to standard HPV vaccination services to see if the combined intervention works to increase HPV vaccination uptake and the use of other health services. The combined intervention includes HPV vaccination given at schools, health facilities, and through community outreach. It also includes education on sexual and reproductive health, counseling, and other health services. Participants in the combined intervention group will: 1. Receive the HPV vaccine at school or at a health facility. 2. Take part in group discussions about sexual and reproductive health. 3. Take part in individual counseling sessions. 4. Use other health services as needed. Participants in the comparison group will receive standard HPV vaccination services, including: • HPV vaccination given at schools, health facilities, and through community outreach.

Participants needed: 700
Trial details
Age: 10-13Biological sex: AllType: InterventionalSponsor: Health Poverty ActionUpdated: Mar 12, 2025Locations: 1
Eligibility criteria

Female aged 10-13 years for HPV vaccination and SRH education [+3]

males and females younger than 10 years or older than 13 years

Status: Recruiting

Correlation Between Smart Phone Overuse, Craniovertebral Angle, Cervical Muscle Endurance and Temporomandibular Proprioception in Adolescents

The study was done to: 1. Investigate the correlation between smart phone overuse and craniovertebral angle in adolescents. 2. Investigate the correlation between smart phone overuse and cervical muscle endurance in adolescents. 3. Investigate the correlation between smart phone overuse and temporomandibular joint proprioception in adolescents.

Participants needed: 160
Trial details
Age: 17-19Biological sex: AllType: ObservationalSponsor: Cairo UniversityUpdated: Mar 6, 2025Locations: 1
Eligibility criteria

Both genders will be included. [+4]

Adolescent who cannot understand or follow instructions. [+6]

Status: Not yet recruiting

Understanding and Acting to Regulate Suicidal Behavior

Data from Santé Publique France show that since the onset of the health crisis (covid-19), there has been an increase in emergency room visits for mood disorders among children under 15 years of age, with a notable rise in the number of visits since early September 2020 compared to previous years. Recent literature considers Dialectical Behavior Therapy (DBT) as the only approach that has demonstrated (albeit weak to moderate) effects on the recurrence of self-harming behaviors. It is within this context, and based on these various findings, that the CARES program was developed (Understanding and Acting to Regulate Emotions and Suicidal Behaviors), aimed at adolescents who have engaged in suicidal behaviors or who have active suicidal ideation. The objective of this study is to compare the CARES program for adolescents alone to the CARES program for adolescents combined with a parent group using Non-Violent Resistance (NVR) on the occurrence of self-harming behaviors among adolescents who have engaged in suicidal acts and/or have active suicidal ideation, six months after the conclusion of the intervention. This is a prospective, randomized, open-label, single-center, controlled study with two parallel arms, with blinded assessment of the outcome measures.

Participants needed: 108
Trial details
Age: 12-16Biological sex: AllType: InterventionalSponsor: University Hospital, MontpellierUpdated: Nov 14, 2024
Eligibility criteria

Age from 12 to 16 years 11 months old [+2]

Intellectual developmental disorder [+9]

Status: Recruiting

Effectiveness of a Multicomponent Intervention to Promote Physical Activity Levels During the School Day (MOVESCHOOL)

Study based a multicomponent school-based intervention during the school-day (i.e., Physically active learning, active breaks, and active recess) on Physical Activity, health, educational, and cognition outcomes in adolescents.

Participants needed: 900
Trial details
Age: 11-16Biological sex: AllType: InterventionalSponsor: University of ExtremaduraUpdated: Sep 19, 2024Locations: 1
Eligibility criteria

Adolescents in 1st, 2nd and 3rd year of ESO. [+3]

Adolescents with any physical disability or health condition that may limit phys... [+1]

Status: Recruiting

Effectiveness of Integrating Physically Active Learning Through Co-teaching in Extremadura: ACTIVA-MENTE Project

Study based on a school-based physically active learning intervention during the school day on physical activity, fitness, health and education outcomes in adolescents.

Participants needed: 800
Trial details
Age: 11-16Biological sex: AllType: InterventionalSponsor: University of ExtremaduraUpdated: Sep 19, 2024Locations: 1
Eligibility criteria

Adolescents in 1st, 2nd, 3rd and 4th year of ESO. [+3]

Adolescents with any physical disability or health condition that may limit phys... [+1]

Status: Recruiting

Centralized Virtual SBIRT for Pediatric Primary Care

Adolescent alcohol and other drug (AOD) use is a significant public health problem which contributes to high levels of mortality, morbidity and healthcare costs in young people, and identification and early intervention for these problems is critical to improving outcomes. Screening, Brief Intervention and Referral to Treatment (SBIRT) in pediatric primary care is an evidence-based strategy for addressing these problems, but has not been widely and systematically implemented, for a variety of reasons, including lack of training and staffing resources to support its implementation. This pragmatic, Type 1 Hybrid Comparative Effectiveness Implementation study will examine whether a centralized, virtually-delivered modality of SBIRT, rapidly accessible by multiple pediatric primary care clinics, can be cost-effectively implemented to improve early identification and treatment for AOD use and comorbid mental health problems among adolescents identified as being at high or severe risk of AOD use disorder during adolescent Well Visits.

Participants needed: 22,320
Trial details
Age: 12-17Biological sex: AllType: InterventionalSponsor: Kaiser PermanenteUpdated: Jul 8, 2024Locations: 1
Eligibility criteria

Not listed