Effectiveness of a Childbirth and Parenthood Preparation Education in Primigravidas

NCT ID: NCT05976776

Last Updated: 2024-07-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

136 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-09-01

Study Completion Date

2024-06-30

Brief Summary

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To investigate the effect of the Childbirth and Parenthood Preparation Education on Maternal Health Needs, Pregnancy-Related Anxiety and Fetal Health Anxiety in Primigravidas. A total of 148 pregnant women are planned to be included in the study. Data will be collected with the 'Pregnant Identification Form', 'Maternal Health Needs Scale', 'Pregnancy-Related Anxiety Scale-Revision 2' and 'Fetal Health Anxiety Inventory. The "Childbirth and Parenthood Preparation Education" program will be applied to the experimental group for a period of four weeks (a month (each week, once a week in total four sessions)). It is thought that the results of the research will contribute to the welfare of pregnant women by reducing maternal health needs, pregnancy-related anxiety and fetal health anxiety levels.

Detailed Description

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To investigate the effect of the Childbirth and Parenthood Preparation Education on Maternal Health Needs, Pregnancy-Related Anxiety and Fetal Health Anxiety in Primigravidas. A total of 148 pregnant women are planned to be included in the study. Data will be collected with the 'Pregnant Identification Form', 'Maternal Health Needs Scale', 'Pregnancy-Related Anxiety Scale-Revision 2' and 'Fetal Health Anxiety Inventory. The "Childbirth and Parenthood Preparation Education" program will be applied to the experimental group for a period of four weeks (a month (each week, once a week in total four sessions)). Within the scope of the "Childbirth and Parenthood Preparation training" program; Physiological and psychological changes in the mother during pregnancy, daily life during pregnancy, smoking, alcohol and substance use during pregnancy, exercise during pregnancy, nutrition and nutritional support during pregnancy, pregnancy follow-ups, routine examinations and immunization, common problems during pregnancy and suggestions for solutions, signs of danger during pregnancy and what to do, risky pregnancies, drug and human medicinal product management during pregnancy, labor process, drug-free methods for coping with labor pain, postpartum period and its characteristics, physiological changes in the mother after birth, psychological changes in puerperium, puerperal role and adaptation, postpartum behaviors , care of the newborn in the postpartum period, postpartum contraception methods will be explained. It is thought that the results of the research will contribute to the welfare of pregnant women by reducing maternal health needs, pregnancy-related anxiety and fetal health anxiety levels.

Conditions

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Pregnancy Related Anxiety

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

A randomized-controlled trial with pretest-posttest control group
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Experimental group

The Childbirth and Parenthood Preparation Education program

Group Type EXPERIMENTAL

The Childbirth and Parenthood Preparation Education

Intervention Type BEHAVIORAL

The "Childbirth and Parenthood Preparation Education" program will be applied to the experimental group for a period of 1 month (each week, once a week in total four sessions).

Control group

No intervention

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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The Childbirth and Parenthood Preparation Education

The "Childbirth and Parenthood Preparation Education" program will be applied to the experimental group for a period of 1 month (each week, once a week in total four sessions).

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Literate
* 18-40 years old
* Primigravida
* Those who volunteered to participate in the research
* Pregnant women who do not have communication and mental difficulties

Exclusion Criteria

* Those who do not fill out the entire questionnaire
* Those with risky pregnancy
* Pregnant women with a previous history of psychiatric illness
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Amasya University

OTHER

Sponsor Role lead

Responsible Party

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Emine Akca

Assist. Prof. Dr. in the Amasya University Midwifery Department

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Emine İbici Akça

Role: PRINCIPAL_INVESTIGATOR

Amasya University

Locations

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Amasya University

Amasya, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Minozzi S, Ambrosi L, Saulle R, Uhm SS, Terplan M, Sinclair JM, Agabio R. Psychosocial and medication interventions to stop or reduce alcohol consumption during pregnancy. Cochrane Database Syst Rev. 2024 Apr 29;4(4):CD015042. doi: 10.1002/14651858.CD015042.pub2.

Reference Type DERIVED
PMID: 38682758 (View on PubMed)

Other Identifiers

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Amasya Un

Identifier Type: -

Identifier Source: org_study_id

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