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Completed

NCT Number: NCT06965647

Effect of Partner-Conducted Fetal Heart Sound Measurement on Maternal and Paternal Attachment

This randomized controlled study aims to evaluate the effect of fetal heart sound (FHS) measurement performed by the partner on prenatal maternal and paternal expectations and attachment levels. A total of 120 couples (60 intervention, 60 control) participated in the study.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

İnönü üniversitesi

Malatya, Turkey (Türkiye)

About this study

This experimental study was conducted to determine the effect of partner-conducted fetal heart sound (FHS) measurement on prenatal maternal and paternal expectations and attachment. The study included 120 couples (60 intervention, 60 control) whose pregnancies were between 28 and 38 weeks, and who were registered at Hasköy Family Health Center in Muş, Turkey. In the intervention group, the father was trained in Leopold maneuvers and performed the FHS measurement twice - once during 28-32 weeks and again during 33-38 weeks of gestation. Data collection tools included the Prenatal Maternity Expectations Scale, Prenatal Paternity Expectations Scale, Prenatal Attachment Inventory, and the Paternal Antenatal Attachment Scale. Data were collected before the first FHS measurement (pre-test) and after the second (post-test). The control group received standard prenatal monitoring by healthcare staff without involving the partner. The study was approved by the Malatya Clinical Research Ethics Committee (Approval No: 2022/3968).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

  • Inclusion Criteria: Women between 28 and 38 weeks of gestation
  • Age between 18 and 45 years
  • Ability to read and write
  • No diagnosed psychiatric illness
  • Healthy pregnancy
  • Attending prenatal visits with their partner

Exclusion criteria

  • Women with diagnosed psychiatric conditions
  • Couples unwilling to participate
  • Incomplete data forms
  • Those who moved out of the study area during follow-up
  • Women without their partners during visits

Treatment and study plan

Partner-Conducted Fetal Heart Sound Measurement

Behavioral

Expectant fathers in the intervention group were trained in basic Leopold maneuvers and fetal heart sound measurement using a Doppler device. Under the supervision of a midwife, fathers located the fetus's back, applied gel, and measured the heart sound during prenatal visits at 28-32 and 33-38 weeks of gestation.

Primary outcomes

  1. Prenatal Paternal Attachment Level

    Time frame: From 28-38 weeks of gestation (approximately 10 weeks)

    Change in paternal attachment scores, measured using the Prenatal Paternal Attachment Scale (PPAS), before and after partner-conducted fetal heart sound measurement.

Secondary outcomes

  1. Prenatal Maternal Attachment Level

    Time frame: From 28-38 weeks of gestation (approximately 10 weeks)

    Change in maternal attachment scores, measured using the Prenatal Attachment Inventory (PAI), before and after the intervention.

  2. Parental Expectations (Mother and Father)

    Time frame: From 28-38 weeks of gestation (approximately 10 weeks)

    Change in maternal and paternal expectations measured using validated Maternity and Paternity Expectation Scales before and after the intervention.

Sponsors and collaborators

Lead sponsor

Inonu University

Other

Registry information

Official study title

The Effect of Partner-Conducted Fetal Heart Sound Measurement on Maternal-Paternal Expectations and Maternal-Paternal Attachment: An Experimental Study

Acronym: FHS-ATTACH

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
May 11, 2025
Registry last updated
May 11, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.