Secondary Traumatic Stress

3

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

Condition / disease
Location
Status: Not yet recruiting

The Effect of Web-Based Compassion-Focused Structured Writing Programs on Well-Being in Midwives Working in Delivery Rooms

This randomized controlled trial aims to compare the effects of a web-based compassion-focused writing program and a reflective writing program on psychological well-being, self-compassion, postpartum trauma-related stress symptoms, and post-traumatic growth in midwives working in delivery rooms.

Participants needed: 90
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Mersin UniversityUpdated: Jul 13, 2026
Eligibility criteria

Working as a midwife in a delivery room between November 1, 2025, and February 1... [+9]

Not working in a delivery room during the specified dates [+7]

Status: Not yet recruiting

Effect of Mindfulness-Based Self-Compassion Program on Self-Compassion, Secondary Traumatic Stress, and Professional Quality of Life in Midwives and Nurses Working in Obstetrics: A Randomized Controlled Trial

This study aims to examine the effect of a Mindfulness-Based Self-Compassion Program on self-compassion levels, secondary traumatic stress, and professional quality of life in midwives and nurses working in obstetrics. Healthcare professionals in this field are frequently exposed to traumatic experiences such as complicated deliveries, perinatal loss, and obstetric emergencies, which may lead to secondary traumatic stress and reduced professional quality of life over time. This study is designed as a pre-test/post-test randomized controlled trial. A total of 80 participants (40 intervention, 40 control) will be recruited from Gaziantep Cengiz Gökçek Obstetrics and Pediatrics Hospital. The intervention group will receive an 8-week Mindfulness-Based Self-Compassion Program (one session per week, 60-90 minutes each). The control group will receive no intervention. Outcomes will be measured before and after the program using validated scales for self-compassion, secondary traumatic stress, and professional quality of life.

Participants needed: 80
Trial details
Biological sex: AllType: InterventionalSponsor: Agri Ibrahim Cecen UniversityUpdated: Jun 11, 2026
Eligibility criteria

Working as a midwife or nurse in obstetrics [+4]

Incomplete or incorrect completion of data collection forms [+4]

Status: Recruiting

A Pilot Study of RISE for Nurse Managers Retreat

The purpose of this study is to determine the feasibility and acceptability of the RISE for Nurse Managers retreat and its impact on occupational and psychological well-being indicators

Participants needed: 16
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: AdventHealthUpdated: Feb 19, 2026Locations: 1
Eligibility criteria

an employed AdventHealth Nurse Manager [+1]

a direct care RN, Nurse Director, Educator, and Executive [+1]