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Recruiting NCT07583199

NCT07583199 The Effect of Student-Midwife Support Circle Intervention on Burnout, Resilience, and Professional Belonging Levels of Midwifery Students

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Clinical Trial Summary
NCT ID NCT07583199
Status Recruiting
Phase
Sponsor Amasya University
Condition Burnout
Study Type INTERVENTIONAL
Enrollment 80 participants
Start Date 2026-04-06
Primary Completion 2026-07-10

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 49 Years
Study Type INTERVENTIONAL
Interventions
Student Midwife Support Circle

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 80 participants in total. It began in 2026-04-06 with a primary completion date of 2026-07-10.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Midwifery students are exposed to multifaceted stressors such as traumatic and unsupportive clinical experiences and psychosocial burdens; this can negatively impact emotional well-being, leading to secondary traumatic stress, burnout, compassion fatigue, and decreased sense of belonging. In this context, there is a growing need for structured and supportive interventions aimed at strengthening students' self-efficacy, resilience, and perceptions of social support. The aim of this research is to determine the effect of the Student Midwife Support Circle Intervention on midwifery students' levels of burnout, resilience, and professional belonging.

Eligibility Criteria

Inclusion Criteria: * Individuals who agree to participate voluntarily in the study * Individuals studying in the field of midwifery Exclusion Criteria: * Individuals who do not agree to participate voluntarily in the study, * Individuals who have previously received Student Midwife Support Circle Intervention

Contact & Investigator

Central Contact

Betül UZUN ÖZER

✉ betul123uzun@gmail.com

📞 05396702942

Frequently Asked Questions

Who can join the NCT07583199 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 49 Years, studying Burnout. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07583199 currently recruiting?

Yes, NCT07583199 is actively recruiting participants. Contact the research team at betul123uzun@gmail.com for enrollment information.

Where is the NCT07583199 trial being conducted?

This trial is being conducted at Amasya, Turkey (Türkiye).

Who is sponsoring the NCT07583199 clinical trial?

NCT07583199 is sponsored by Amasya University. The trial plans to enroll 80 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology