Emotional Freedom Technique and Music Therapy in High-Risk Pregnancy for PPROM
Official title: The Effect of Emotional Freedom Technique and Music Therapy Applied to High-Risk Pregnant Women on Maternal Psychological Status, Coping Methods, and Non-Stress Test Findings: A Randomized Controlled Trial
Run by Selcuk University · NCT07559071 · Data updated 2026-11-12
This study tests whether emotional freedom techniques and music therapy can help pregnant women with PPROM or PROM cope better and feel less stress.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | Women only |
| Enrollment | 177 (estimated) |
| Sponsor | Selcuk University Academic / other |
| Locations | 1 site (Konya, Konya) |
| Status | Recruiting |
| Started | June 1, 2026 |
| Main results expected | March 2027 |
| Study ends | March 2027 |
| Registry record updated | September 10, 2026 |
| Trial ID | NCT07559071 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are Turkish-speaking women aged 18 or older with PPROM between 28+0 and 35+5 weeks gestation, singleton pregnancy, and a SUDS score of at least 1.
✕Probably not a fit
Participants with active labor, other obstetric complications, major fetal anomalies, or conditions requiring emergency intervention may not benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This interventional study examines the use of emotional freedom technique (EFT) and music therapy in women with high-risk pregnancies due to PPROM or PROM. Eligible participants are Turkish-speaking women aged 18 or older, 28+0 to 35+5 weeks gestation, with PPROM, and a baseline distress score. The approach appears to involve non-pharmacologic, mind-body therapies delivered during pregnancy to potentially influence maternal stress and fetal well-being, as assessed by standard obstetric and psychological measures. Outcomes may include maternal psychological status and fetal well-being indicators, such as non-stress test patterns. The study is conducted at Konya City Hospital with Selcuk University as the lead sponsor.
Why it matters
Potential benefit: If successful, participants may experience reduced stress and improved coping during a high-risk pregnancy.
How similar studies have gone: Evidence in related areas suggests mind-body interventions can reduce distress, but similar approaches in PPROM/PROM pregnancies are not well established.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Women aged 18 years and older * Able to speak and understand Turkish * Diagnosed with preterm premature rupture of membranes (PPROM) * Gestational age between 28+0 and 35+5 weeks * Score of ≥1 on the Subjective Units of Disturbance Scale (SUDS) * Singleton pregnancy * Able and willing to communicate and participate in the study Exclusion Criteria: * Pregnancy achieved via assisted reproductive technologies * Presence of any obstetric complication other than PPROM * Presence of major fetal anomalies * Active labor at the time of recruitment * Hearing impairment * Presence of infection, wounds, or scars at tapping sites (for EFT application) * History of severe psychiatric disorder or currently receiving psychiatric treatment * Any maternal or fetal condition requiring emergency medical intervention
Where it's running
-
Konya City Hospital
Konya, Konya, Turkey (Türkiye) Recruiting
Study contacts
- Study coordinator: Süreyya Kılıç, PhD(c)
- Email: sureyyakilic117@gmail.com
- Phone: +90 501 578 99 08
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.