| NCT ID | NCT07485790 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Amasya University |
| Condition | Sleep Disorder |
| Study Type | INTERVENTIONAL |
| Enrollment | 70 participants |
| Start Date | 2026-03-15 |
| Primary Completion | 2026-08-01 |
Eligibility & Interventions
Eligibility Fast-Check
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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 70 participants in total. It began in 2026-03-15 with a primary completion date of 2026-08-01.
⚠ 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
It is thought that a yoga intervention administered to pregnant women will reduce stress levels, enhance sexual quality of life, and positively affect sleep habits. According to the power analysis results, the study must include at least 70 pregnant women (35 in the experimental group and 35 in the control group). Data will be collected through a Personal Information Form, the Perceived Stress Scale (PSS), the Sexual Quality of Life Questionnaire-Female (SQLQ-F), and a Sleep Habits Form. In this study, the yoga practice will be administered to the pregnant women in the experimental group by the researcher.
Eligibility Criteria
Inclusion Criteria: * In their third trimester, * Able to read and write in Turkish, * Use a smartphone and have internet access, * Have no communication barriers, * Voluntarily agree to participate in the research. Exclusion Criteria: * Pregnant women with any risk factors during pregnancy, * Pregnant women with any chronic illness, * Pregnant women with a diagnosed psychological problem, * Pregnant women with any exercise restrictions imposed by a physician, * Pregnant women participating in a different training program (meditation, relaxation, etc.)
Contact & Investigator
Emine İbici Akça, PhD
PRINCIPAL INVESTIGATOR
Amasya University
Frequently Asked Questions
Who can join the NCT07485790 clinical trial?
This trial is open to female participants only, aged 18 Years or older, studying Sleep Disorder. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT07485790 currently recruiting?
Yes, NCT07485790 is actively recruiting participants. Contact the research team at emine.akca@amasya.edu.tr for enrollment information.
Where is the NCT07485790 trial being conducted?
This trial is being conducted at Amasya, Turkey (Türkiye).
Who is sponsoring the NCT07485790 clinical trial?
NCT07485790 is sponsored by Amasya University. The principal investigator is Emine İbici Akça, PhD at Amasya University. The trial plans to enroll 70 participants.