Young Adult Females

4

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

Condition / disease
Location
Status: Recruiting

Effects of Passive Recovery Methods After High-Intensity Cycling Exercise

This randomized crossover trial will investigate the acute effects of five passive recovery interventions following a standardized high-intensity cycling exercise protocol. Participants will complete one supervised high-intensity cycling session per week for five consecutive weeks. Immediately after each exercise session, participants will receive one of five recovery interventions: compression therapy, vacuum therapy, kinesiology taping, passive rest, or classical massage. The order of the interventions will be randomized according to a balanced crossover sequence. Each participant will experience all five recovery interventions during the study period. Outcomes related to post-exercise recovery will be assessed across intervention periods.

Participants needed: 10
Trial details
Age: 18-30Biological sex: AllType: InterventionalSponsor: Pamukkale UniversityUpdated: Jun 30, 2026Locations: 1
Eligibility criteria

Healthy adult volunteers aged 18-35 years [+7]

Presence of acute or chronic musculoskeletal injury [+7]

Status: Not yet recruiting

Trauma-Informed Yoga Intervention in Young Women

The aim of this study is to evaluate the effects of a trauma-informed yoga intervention on psychological trauma symptoms, difficulties in emotion regulation, and interoceptive awareness in young adult women.

Participants needed: 46
Trial details
Age: 18-25Biological sex: FemaleType: InterventionalSponsor: Saglik Bilimleri UniversitesiUpdated: May 15, 2026Locations: 1
Eligibility criteria

Being a woman aged 18-25 years [+4]

Inability to provide reliable responses due to the presence of active psychotic... [+4]

Status: Recruiting

Sexual Functıon in Young Women After Breast Cancer Surgery

The aim of this observational study was to analyse sexual function in young women after breast cancer surgery. The main question it aims to answer is Sexual function in young women after breast cancer surgery changes during the one-year follow-up period. Participants will answer demographic information, Female Sexual Function Scale, Breast-Q and Body Perception Scale about their sexual function, quality of life and body perception. These will be recorded before surgery and repeated 6 weeks, 6 months and 1 year after surgery.

Participants needed: 52
Trial details
Age: 18-50Biological sex: FemaleType: ObservationalSponsor: ATİYE KAŞ ÖZDEMİRUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Individuals scheduled for surgery for breast cancer [+3]

Previous breast cancer surgery [+5]

Status: Recruiting

Non-Diet Nutrition Education and Its Effects on Eating Behavior, Body Image, and Well-Being in Adult Women

The goal of this clinical trial is to evaluate whether a non-diet nutrition education program can improve eating behaviors, body image, and well-being in normal-BMI women aged 19-35 years. The main questions it aims to answer are: * Does participation in an 8-week non-diet nutrition education program improve eating behavior, body image, and well-being over time in the intervention group compared to the control group? * Is there a significant difference between the intervention and control groups in eating behavior, body image, and well-being after the intervention? Researchers will compare an intervention group receiving an 8-week non-diet nutrition education with a control group receiving no intervention, to see if the program leads to improvements in psychological and behavioral outcomes without focusing on weight loss. Participants will: * Complete pre- and post-intervention assessments, including validated questionnaires on eating behavior (DEBQ, FCQ, IES-2), body image (BAS, Stunkard Figure Rating Scale), and psychological well-being (WHO-5, Rosenberg Self-Esteem Scale), as well as a 3-day food diary. * Be randomly assigned to either the intervention group (8-week online non-diet nutrition education sessions) or the control group (no intervention). * Engage in 8 weekly, 60-minute sessions focused on intuitive eating, body acceptance, and health-promoting nutrition.

Participants needed: 52
Trial details
Age: 19-35Biological sex: FemaleType: InterventionalSponsor: Tuğba TÜRKCANUpdated: Aug 8, 2025Locations: 1
Eligibility criteria

Female, [+2]

Pregnant or breastfeeding, [+3]