Effectiveness of a Childbirth and Parenthood Preparation Education in Primigravidas

Sponsor
Amasya University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05976776
Collaborator
(none)
148
1
2
10
14.9

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: The Childbirth and Parenthood Preparation Education
N/A

Detailed Description

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
148 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
A randomized-controlled trial with pretest-posttest control groupA randomized-controlled trial with pretest-posttest control group
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Effectiveness of a Childbirth and Parenthood Preparation Education on Maternal Health Needs, Pregnancy-Related Anxiety and Fetal Health Anxiety in Primigravidas
Anticipated Study Start Date :
Sep 1, 2023
Anticipated Primary Completion Date :
Mar 31, 2024
Anticipated Study Completion Date :
Jun 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental group

The Childbirth and Parenthood Preparation Education program

Behavioral: 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).

No Intervention: Control group

No intervention

Outcome Measures

Primary Outcome Measures

  1. Levels of Maternal Health Needs [1 months]

    Maternal Health Needs is one of the primary outcomes. This will be measured using 'Maternal Health Needs Scale (MHNS) '. The minimum score that can be obtained from the scale is "23", the maximum score is "115", and as the scale score increases, maternal health needs also increase.

Secondary Outcome Measures

  1. Pregnancy-Related Anxiety Levels [1 months]

    Pregnancy related anxiety level is another outcomes. This will be mesured using "Pregnancy-Related Anxiety Scale- Revision 2". The minimum score that can be obtained from the scale is "11", the maximum score is "55", as the score obtained from the scale increases, the level of anxiety in pregnancy also increases.

  2. Fetal Health Anxiety Levels [1 months]

    Fetal Health Anxiety level is another outcomes. This will be mesured using "Fetal Health Anxiety Inventory (FHAI)". The minimum score that can be obtained from the scale is "0", the maximum score is "42", as the total score from the scale increases, the level of fetal health anxiety increases.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Amasya University Amasya Turkey 05100

Sponsors and Collaborators

  • Amasya University

Investigators

  • Principal Investigator: Emine İbici Akça, Amasya University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Emine Akca, Assist. Prof. Dr. in the Amasya University Midwifery Department, Amasya University
ClinicalTrials.gov Identifier:
NCT05976776
Other Study ID Numbers:
  • Amasya Un
First Posted:
Aug 4, 2023
Last Update Posted:
Aug 9, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Emine Akca, Assist. Prof. Dr. in the Amasya University Midwifery Department, Amasya University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 9, 2023