Actively Recruiting

Phase Not Applicable
Age: 19Years - 35Years
All Genders
Healthy Volunteers
NCT07263750

Effect of Haptonomy on Prenatal Attachment and Fear of Childbirth in Primiparous Couples

Led by Nigde Omer Halisdemir University · Updated on 2026-02-03

144

Participants Needed

1

Research Sites

53 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study was planned to evaluate the effect of haptonomy practice for primiparous pregnant women and their partners on prenatal attachment and fear of childbirth.

CONDITIONS

Official Title

Effect of Haptonomy on Prenatal Attachment and Fear of Childbirth in Primiparous Couples

Who Can Participate

Age: 19Years - 35Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • At least a primary school graduate
  • Between 24 and 26 weeks of pregnancy based on ultrasound or last menstrual period
  • Primiparous (first pregnancy)
  • No history of abortion or curettage
  • Pregnancy is planned and desired
  • Desired baby gender
  • Living with spouse
  • Attended pregnancy classes
  • Able to use technology such as computers and mobile phones to watch videos
  • No barriers to understanding questions and responding
  • No previous training on fear of childbirth or prenatal bonding
  • Not previously trained in or practiced haptonomy
  • Not undergoing infertility treatment
  • Between 19 and 35 years old
Not Eligible

You will not qualify if you...

  • Pregnant beyond 26 weeks
  • Living separately from spouse
  • Unplanned or unwanted pregnancy
  • No preference for baby's gender
  • Unable to use technology
  • High-risk pregnancy
  • Previously received training on fear of childbirth or prenatal bonding
  • Previously received training in or practiced haptonomy
  • Decided to stop haptonomy practice after starting the study or gave birth prematurely before completing sessions

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sivas Cumhuriyet University

Merkez, Sivas, Turkey (Türkiye), 58000

Actively Recruiting

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Research Team

N

Nilüfer Tuğut, Prof. Dr.

CONTACT

S

sibel dilmen, lectuer

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

2

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