The Door to the Womb at Birth: Haptonomy

Last updated: August 26, 2024
Sponsor: Trakya University
Overall Status: Completed

Phase

N/A

Condition

Pregnancy Complications

Mild Cognitive Impairment

Memory Loss

Treatment

Haptonomy

Clinical Study ID

NCT06508554
2023-SBB-0594
  • Ages 18-49
  • Female
  • Accepts Healthy Volunteers

Study Summary

Purpose: This study aimed to examine the effect of haptonomy application on the expectant mother's birth expectations, experiences, birth self-efficacy, birth memory and reminder during labor.

Materials and Methods: The prospective, double-blind, randomized controlled study is conducted between 10.10.2023-10.08.2024, with n=80 (40=control, 40=intervention) women volunteering to participate in the study randomly in two groups: intervention and control. In the study, the Personal Data Collection Form prepared by reviewing the literature, Wijma Birth Expectation/Experience Scale (W-DEQ) A and B version, Labor Self-Efficacy Scale (DEÖÖ) and Birth Memory and Recall Scale (DHÖ) were used.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Married and pregnant women,

  • ≥ 18 years old,

  • Able to read, write and understand Turkish,

  • Living in the city center where the study is conducted,

  • Does not have any physical or psychological health problems for herself or her baby,

  • Having a spontaneous pregnancy at 28.< gestational weeks,

  • Those who have not received haptonomy application before,

  • Pregnant women who agreed to participate in the study were included.

Exclusion

Exclusion Criteria:

  • Those with psychological and chronic health problems,

  • Pregnant women who did not agree to participate in the study were not included.

Study Design

Total Participants: 80
Treatment Group(s): 1
Primary Treatment: Haptonomy
Phase:
Study Start date:
October 10, 2023
Estimated Completion Date:
August 01, 2024

Connect with a study center

  • Bartın University

    Bartin, 78100
    Turkey

    Site Not Available

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