Coping

3

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

Condition / disease
Location
Status: Recruiting

TAG TEAM - Trans Adolescent Group Therapy

This project will study the effect of the TAG TEAM group CBT program on the mental health of trans and gender diverse adolescents. TAG TEAM was co-designed by researchers and clinicians with a group of trans and gender diverse young people to help trans and gender diverse adolescents understand and cope with minority stress. Minority stress includes experiences like discrimination and rejection. TAG TEAM focuses on learning and practicing skills to support mental health and wellbeing. It also includes group discussions and activities with other trans and gender diverse young people. TAG TEAM groups are run by a psychologist and a trans peer facilitator. A trans peer facilitator is a trans and gender diverse person who is there to share their experience of being trans and to support participants in the group sessions.

Participants needed: 142
Trial details
Age: 12-17Biological sex: AllType: InterventionalSponsor: Murdoch Childrens Research InstituteUpdated: Jun 5, 2026Locations: 1
Eligibility criteria

Identifies as trans, non-binary, or gender diverse [+9]

Status: Recruiting

The Effectiveness and Acceptability of Formal Versus Informal Mindful Self-Compassion for Adolescents

The goal of this clinical trial is to learn if two types of mindful self-compassion programs work to improve coping in adolescents. The investigators will also learn about adolescents' liking of, and the other potential mental health and academic benefits of, these programs. The main questions this clinical trial aims to answer are: * Do two types of mindful self-compassion programs improve coping in adolescents? * Do two types of mindful self-compassion programs improve mental health (e.g., stress, anxiety, depression) and academic outcomes (e.g., academic engagement) in adolescents? * How satisfactory are two types of mindful self-compassion programs for adolescents? To do this, the investigators will compare adolescents who complete two types of mindful self-compassion programs to adolescents in a "waitlist control" condition (who complete no study tasks during the program period, but will have the opportunity to complete the program at the end of the study). Participants will: * Complete a brief phone interview to confirm their eligibility (15 min) * Complete an online survey including questions about coping, mental health, and academic engagement (30 min) * Complete a live, online, four-week-long mindful self-compassion program OR no study tasks during this four-week period (if randomly assigned to a waitlist condition) * Complete an online survey 1 week after the 4-week period, including questions about coping, mental health, and academic engagement, as well as their liking of the program they completed (if applicable) * Complete an online survey 1 month after the 4-week period, including questions about coping, mental health, and academic engagement * (Waitlist condition only) Have the opportunity to complete one of the two mindful self-compassion programs after the study had ended

Participants needed: 135
Trial details
Age: 14-19Biological sex: AllType: InterventionalSponsor: Cambridge Health AllianceUpdated: Apr 20, 2026Locations: 1
Eligibility criteria

Be 14-19 years of age for the duration of the study; [+4]

Current or past-year treatment with mindfulness-based psychotherapy (e.g., MBCT,... [+8]

Status: Not yet recruiting

CesiKids Trial: Enhancing Psychological Resilience in Adolescents With Cancer

This study will develop and evaluate a mobile-based co-design intervention (CesiKids) to enhance psychosocial resilience in hospitalized adolescents aged 12-18 diagnosed with cancer. The program will be created using Bronfenbrenner's Ecological Systems Theory and designed in collaboration with nurses, recovered adolescents, and parents. A randomized controlled design will be used. The intervention group will participate in a four-week structured program, while the control group will receive standard care. Psychosocial resilience and coping outcomes will be assessed at baseline, post-intervention, and follow-up. This research aims to offer an evidence-based, scalable model to support resilience among adolescents with cancer in clinical settings.

Participants needed: 36
Trial details
Age: 12-18Biological sex: AllType: InterventionalSponsor: Eskisehir Osmangazi UniversityUpdated: Nov 14, 2025Locations: 1
Eligibility criteria

Parents have provided informed consent after receiving information, [+6]

Receiving hematopoietic stem cell transplantation treatment, [+4]