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NCT06734754
The Effect of Fetal Heart Sound Played by Parents Diagnosed With Risky Pregnancy on Attachment and Anxiety
NA trial testing fetal heart sound listening in Attachment in 272 participants. Completed in 1 March 2025.
10 December 2024
Quick facts
| Lead sponsor | Inonu University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | single |
| Primary purpose | supportive care |
| Enrollment | 272 |
| Start date | 1 February 2024 |
| Primary completion | 10 December 2024 |
| Estimated completion | 1 March 2025 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- fetal heart sound listening
Conditions studied
- Attachment — all drugs for Attachment →
- Risk Pregnancy — all drugs for Risk Pregnancy →
- Anxiety — all drugs for Anxiety →
Sponsor
Inonu University
Who can join
Adults 16 to 55, any sex, with Attachment or Risk Pregnancy. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The research was designed as a randomized controlled experimental type to determine the effect of fetal heart sound played to parents diagnosed with risky pregnancies on attachment and anxiety. With the results obtained from this study, it is aimed to contribute to the limited literature on the effect of fetal heart sound played to parents diagnosed with risky pregnancy on attachment and anxiety. Research question or Hypothesis(ies) and Purpose(s): The purpose of this study is to determine the effect of fetal heart sound played to parents diagnosed with high-risk pregnancy on attachment and anxiety. H1-a: Listening to the fetal heart sound reduces the anxiety level of the expectant mother. H1-b: Listening to the fetal heart sound increases the maternal attachment of the expectant mother. H1-c: Listening to the fetal heart sound reduces the anxiety level of the expectant father. H1-d: Listening to the fetal heart sound increases the paternal attachment of the expectant father. The research will be conducted on 2 groups: 1 experimental and 1 control group. In order to obtain pre-test data of the research, couples will fill in the determined measurement tools. The couples' contact information will be recorded, their appointment dates will be determined and an appointment card will be issued. The intervention applied by the researcher to the participants in the experimental group will be completed in 7 days. At the end of the 7th day, post-test data will be obtained using measurement tools. Pretest data will be obtained using measurement tools in the first interview with the control group. No interventional intervention will be applied to the participants in the control group by the researcher. Post-test data will be obtained 7 days later by applying the same measurement tools.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06734754
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06734754 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Inonu University
- Last refreshed: 9 May 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06734754.
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