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The Effect of Prenatal Haptonomy on Anxiety, Distress and Psychological Well-being

NCT05494840 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 102

Last updated 2024-01-08

No results posted yet for this study

Summary

Introduction:Anksiyete experienced during prenatal can increase Distress, cause negative perinatal outcomes, and adversely affect the psychological well-being. This study will conducted to determine the effect of prenatal haptonomy on pregnancy-related anxiety, distress and psychological well-being.

Methods: The population of the randomized controlled experimental study will consist of 102 primiparous pregnant women within the gestational weeks 22-27 who presented to the pregnant school of a state hospital in Turkey (34 first experimental group, 34 second experimental group, 34 control group).

Conditions

  • First Pregnancy

Interventions

BEHAVIORAL

Haptonomy

Haptonomy, as a field dealing with emotional contact through touch, describe the relationship between parents and the unborn baby.

Sponsors & Collaborators

  • Hilal Özbek

    lead OTHER

Principal Investigators

  • Hilal Özbek · Tokat Gaziosmanpaşa University

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-09-15
Primary Completion
2023-12-30
Completion
2023-12-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05494840 on ClinicalTrials.gov