Young Adult

10

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

Condition / disease
Location
Status: Not yet recruiting

Designing a Smoking Intervention for Youth Smokers

This study aims to develop a typology-based intervention delivered by smoking cessation (SC) counsellors to prevent smoking relapse in ex-smokers who recently quit. The two main research questions include (1) Can a typology-based smoking relapse prevention intervention be feasible and accepted by the smokers and SC counsellors who deliver the new intervention? (2) What is the preliminary evidence on the efficacy of the typology-based smoking relapse prevention to increase tobacco abstinence in ex-smokers who have recently quit? If the intervention shows at least a small effect size (i.e. risk ratio\>1.3), or the intervention is feasible while modifications can potentially increase the efficacy, a future definitive RCT is warranted.

Participants needed: 100
Trial details
Age: Up to 25Biological sex: AllType: InterventionalSponsor: The University of Hong KongUpdated: Jun 2, 2026Locations: 1
Eligibility criteria

Hong Kong citizens [+11]

Have unstable physical or psychological conditions as advised by doctors or coun... [+4]

Status: Recruiting

Intratumoral DNX-2401 for High Grade Pediatric Brain Tumors

The goal of this clinical trial is to learn if intratumoral administration of DNX-2401 works to treat recurrent and refractory high grade brain tumors in children and young adults. It will also learn about the safety of DNX-2401. The main questions it aims to answer are: * Does a single intratumoral administration of DNX-2401 elicit tumor response and improve survival? * Is a single intratumoral administration of DNX-2401 safe and well tolerated? Participants will: * Undergo surgery for tumor biopsy followed by a single intratumoral administration of DNX-2401 * Visit the clinic periodically for checkups and tests

Participants needed: 39
Trial details
Phase: Phase 2Age: 1-25Biological sex: AllType: InterventionalSponsor: Clinica Universidad de Navarra, Universidad de NavarraUpdated: May 27, 2026Locations: 2
Eligibility criteria

The participant or participant's parents or legally acceptable representatives (... [+13]

Any medical or psychological condition or disease that might interfere with the... [+12]

Status: Not yet recruiting

Plantar Pressure and Pain in Young Adults

The musculoskeletal system represents a holistic movement organization emerging from the integrated function of the central nervous system, musculoskeletal structures, and joint complexes. This organization is defined in the literature as the kinetic chain, characterized by the sequential and coordinated activation of body segments to enable distal segments to perform activities with optimal speed, position, and timing. The efficiency of the kinetic chain depends on optimal length-tension relationships, neuromuscular control, and balanced load transfer between segments. As the initial point of contact with the ground, the foot functions not merely as a passive support surface but as a dynamic structure actively involved in postural control, balance, and the regulation of ground reaction forces. Plantar pressure distribution and Center of Pressure (CoP) dynamics are considered objective indicators of foot-ground interaction. Due to its complex anatomical and biomechanical structure, any mechanical disturbance within the foot can influence the loading patterns of the entire kinetic chain.Abnormal plantar pressure distribution-characterized by increased peak pressures, altered forefoot-rearfoot load ratios, and increased CoP variability-may lead to compensatory load redistribution in proximal joints. These compensations have been associated with altered motor strategies, reduced neuromuscular control, and impaired shock absorption. Consequently, such alterations may contribute to the development of pain in proximal regions. This suggests a potential association between plantar pressure patterns and pain localization and severity in young adults.

Participants needed: 53
Trial details
Age: 18-35Biological sex: AllType: ObservationalSponsor: Fenerbahce UniversityUpdated: May 6, 2026Locations: 1Duration: 1 Day
Eligibility criteria

Young adults aged between 18 and 35 years [+5]

History of a foot deformity diagnosed during childhood [+3]

Status: Recruiting

Brentuximab Vedotin for Newly Diagnosed cHL in Chinese CAYA Based on PET/CT Assessment

Generally, pediatric patients tolerate acute toxicities but are vulnerable to late effects. Thus, increasing chemotherapy intensity to achieve more rapid complete early response to limit radiation therapy is worth testing. In this CCCG-HL-2024 study, Brentuximab vedotin (Bv) was used to replace VCR and bleomycin in the ABVE-PC regimen in the previous CCCG-HD-2018 study, respectively, to form a Bv-AEPC regimen for the treatment of newly diagnosed classic Hodgkin lymphoma (cHL) in children, adolescents and young adults. On the premise of maintaining a 4-year event free survival (EFS)\>90% in the low-, intermediate-and high-risk groups, increase the early assessment complete response rate (the overall early complete response rate increased by 20%, that is, from 54.0% to 74.0%) to further reduce the proportion of children receiving radiotherapy to benefit them.

Participants needed: 96
Trial details
Phase: Phase 2, Phase 3Age: 2-35Biological sex: AllType: InterventionalSponsor: Children's Cancer Group, ChinaUpdated: Mar 19, 2026Locations: 1
Eligibility criteria

Ages >=2~<35 years at the time of enrollment; [+3]

Patients with nodular lymphocyte-predominant HL; [+3]

Status: Recruiting

Alcohol-ROC-Training

The goal of the proposed study is to examine whether brief training in regulation of craving (ROC-T) affects alcohol drinking. The study will consist of a basic screening (phone and online), and in person visit to determine eligibility and conduct pre-intervention baseline assessments, 1-4 training (ROC-T) visits, a post-intervention assessment visit, and 1-2 phone/online follow up assessments.The two active conditions of ROC-T are based on cognitive-behavioral treatments (CBT) and mindfulness-based treatments (MBT).

Participants needed: 177
Trial details
Age: 18-26Biological sex: AllType: InterventionalSponsor: Yale UniversityUpdated: Feb 19, 2026Locations: 2
Eligibility criteria

Not listed

Status: Recruiting

Optimizing the AYA Survivors' Coping and Emotional Needs Toolkit

Our team has developed a digital intervention that aims to help adolescent and young adult cancer survivors (AYAs) manage symptoms of depression. This tool includes one psychoeducation component and four components that are based on evidence-based interventions for depression. The goal of this study is to test which component or combination of components meaningfully contribute to improvements in depressive symptoms among AYAs.

Participants needed: 208
Trial details
Age: 15-39Biological sex: AllType: InterventionalSponsor: East Carolina UniversityUpdated: Jan 7, 2026Locations: 2
Eligibility criteria

Age at enrollment (adolescents 15-17, emerging adults 18-25, young adults 26-39) [+4]

Mental Health: Current diagnosis of severe or persistent mental illness [+1]

Status: Recruiting

Comparing the Effects of Smart App-Assited Super-Slow Jogging and Stationary Cycling on Respiratory Function and Aerobic Fitness in College Students

As health awareness continues to rise, more people are prioritizing exercise to improve physical condition and enhance overall fitness. For those lacking exercise habits, selecting a simple, accessible, and effective workout becomes crucial. Against a backdrop of prolonged sitting and inactivity, "super slow jogging" is gaining attention. This aerobic exercise involves a slow walking pace and low intensity, yet burns more calories than regular walking, making it an ideal entry-level activity for beginners or those with lower fitness levels. This study aims to investigate whether incorporating super slow jogging training can effectively enhance cardiorespiratory fitness and respiratory function, comparing its outcomes with other exercise types. The purpose of this experiment is academic research, primarily exploring the impact of exercise intervention on physiological functions. It is not intended for health screening or medical diagnosis.

Participants needed: 60
Trial details
Age: 18-25Biological sex: AllType: InterventionalSponsor: Fooyin UniversityUpdated: Dec 30, 2025Locations: 1
Eligibility criteria

required no regular exercise training in the past six months [+1]

musculoskeletal limitations that prevented cycling exercise [+5]

Status: Recruiting

Risk Prediction of Disease Progression in Early-Onset Coronary Atherosclerosis

This study is part of a nationwide research project in China that aims to better understand how coronary artery disease develops and progresses in young adults. The study will enroll approximately 10,000 participants aged 45 years or younger who undergo coronary CT scans at multiple hospitals across China. Information collected at enrollment includes basic health information, cardiovascular risk factors, blood test results, medication use, lifestyle habits, and, for some participants, genetic data. Participants will undergo follow-up coronary CT scans after several years to evaluate changes in coronary artery plaque and disease progression. By analyzing these clinical and imaging data, the study aims to identify factors associated with disease progression and to develop prediction models that may help estimate an individual's future risk of coronary plaque progression and cardiovascular events. The results of this study may contribute to improved risk assessment and early prevention strategies for coronary artery disease in young populations.

Participants needed: 10,000
Trial details
Age: 18-45Biological sex: AllType: ObservationalSponsor: Fu Wai Hospital, Beijing, ChinaUpdated: Jan 5, 2026Locations: 1Duration: 3 Years
Eligibility criteria

Age between 18 and 45 years at the time of enrollment. [+2]

Inability or unwillingness to complete follow-up assessments. [+6]

Status: Not yet recruiting

An Exploratory Feasibility Study

This study explores the feasibility of ContextWell, a well-being education programme that combines an online webinar with an AI-powered behavioural nudging system. The programme aims to support university students, particularly those in healthcare disciplines, in enhancing well-being and adopting healthier lifestyle habits. The primary objective is to determine whether the programme can be feasibly delivered within university settings. A secondary objective is to assess its potential to improve student well-being and encourage behavioural changes aligned with lifestyle medicine principles. The intervention builds on the understanding that healthcare professionals' lifestyle habits and well-being have a direct impact on patient care. Focusing on healthcare students helps advance the integration of lifestyle medicine within health education and clinical practice. This single-group feasibility study delivers the full intervention to all participants. Students participate in an online well-being webinar and receive AI-generated behavioural prompts designed to promote self-awareness and healthier daily choices. Key evaluation measures will indicated the feasibility of the programme among young adults in academic environments. Participant feedback and initial outcomes will support future development and inform larger-scale research.

Participants needed: 12
Trial details
Age: 18-30Biological sex: AllType: InterventionalSponsor: University College DublinUpdated: Jun 19, 2025Locations: 1
Eligibility criteria

Not listed

Status: Recruiting

Cardiovascular Longitudinal ALSPAC Research Investigations Following Hypertensive Pregnancy in Young Adulthood

The purpose of this study is to understand more about why young people who were born to a hypertensive pregnancy may have increased risk of high blood pressure and are often at increased risk of heart and blood vessel disease later in life.

Participants needed: 200
Trial details
Age: 30-40Biological sex: AllType: ObservationalSponsor: University of OxfordUpdated: Jan 12, 2023Locations: 1
Eligibility criteria

Participant is willing and able to give informed consent for participation in th... [+4]

Pregnant or lactating when they are due to attend for study visit 1 [+5]