Clinical trial Recruiting at 1 site Interventional Ages 18 and up Women only

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.

More High Risk Pregnancy trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexWomen only
Enrollment177 (estimated)
SponsorSelcuk University
Academic / other
Locations1 site (Konya, Konya)
StatusRecruiting
StartedJune 1, 2026
Main results expectedMarch 2027
Study endsMarch 2027
Registry record updatedSeptember 10, 2026
Trial IDNCT07559071 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

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.