NCT07187557

Brief Summary

The pregnancy period, during which physiological, psychological and social changes occur, can negatively affect women mentally. It is stated that women's concerns about their own and their baby's health, anxiety and fear regarding birth, the uncertainty of the postpartum process and ambivalent feelings experienced cause negative mood changes. During pregnancy, body image dissatisfaction may develop due to weight gain, posture and skin changes, and this may cause women to experience depressive symptoms. Psychological changes such as depression, anxiety and stress experienced during pregnancy cause women to experience fear and anxiety regarding birth. Fear of birth, which is affected by many factors, also affects women's birth preferences and method. Fear of birth also affects women's psychological well-being in the postpartum period. Interventions are needed to ensure and maintain the psychological resilience of pregnant women. The aim of this study is to determine the effect of a self-compassion-based birth preparation program on self-compassion, body image, fear of birth, depression, anxiety and stress.

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
1mo left

Started Sep 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress84%
Sep 2025Jun 2026

First Submitted

Initial submission to the registry

June 11, 2025

Completed
3 months until next milestone

First Posted

Study publicly available on registry

September 23, 2025

Completed
1 day until next milestone

Study Start

First participant enrolled

September 24, 2025

Completed
9 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 12, 2026

Expected
8 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 20, 2026

Last Updated

November 18, 2025

Status Verified

November 1, 2025

Enrollment Period

9 months

First QC Date

June 11, 2025

Last Update Submit

November 14, 2025

Conditions

Outcome Measures

Primary Outcomes (7)

  • The Effect of Self-Compassion Based Birth Preparation Program on Self-Compassion, Body Image, Fear of Childbirth, Depression, Anxiety and Stress in Pregnant Women

    This study aims to determine the effects of a self-compassion-based birth preparation program on self-compassion, body image, fear of childbirth, depression, anxiety and stress in pregnant women

    from june 2025 to june 2026

  • Personal Information Form

    Developed by the researchers based on literature, the form consists of questions regarding the socio-demographic and obstetric characteristics of pregnant women, such as their age, educational status, employment status, chronic disease status, number of pregnancies, gestational age, and number of children.

    In the 28th week of pregnancy

  • Self-Compassion Scale Short Form

    The Self-Compassion Scale Short Form, developed by Raes et al. (2011), is used to measure an individual's level of self-compassion. The scale was adapted into Turkish by Yıldırım and Sarı (2018). The single-dimension scale consists of 11 items and a 5-point Likert-type scale. High scores indicate high levels of self-compassion. The lowest possible score is 11, and the highest is 55. There is no cut-off score for the scale

    At 28 weeks of pregnancy, after completing the program (4 weeks later) 1st month postpartum 3rd month postpartum

  • Pregnancy Body Image Scale

    The Pregnancy Body Image Scale was developed by Watson et al. (2017) and adapted into Turkish by Gün Kakaşçı et al. (2022). As the total score on the scale increases, the perception of negative body image in pregnant women increases. The Cronbach's alpha coefficient for the entire scale was 0.90 and ranged from 0.65 to 0.94 for its subscales

    At 28 weeks of pregnancy, after completing the program (4 weeks later)

  • Wijma Childbirth Expectation/Experience Scale Version A

    This six-point Likert-type scale, consisting of 33 items covering childbirth-related fears, is scored from 0 to 5, with 0 being interpreted as completely and 5 being interpreted as not at all. The minimum score on the W-DEQ-A is 0, and the maximum score is 165. As women's scale scores increase, their fear of childbirth increases. W-DEQ-A scores are graded into four groups: mild fear of childbirth (W-DEQ-A score ≤37), moderate fear of childbirth (W-DEQ-A scores between 38 and 65), severe fear of childbirth (W-DEQ-A scores between 66 and 84), and clinical fear of childbirth (W-DEQ-A scores ≥85.

    At 28 weeks of pregnancy, after completing the program (4 weeks later)

  • Wijma Childbirth Expectation/Experience Scale Version B

    The Wijma Childbirth Expectation/Experience Scale Version B (W-DEQ-B) was developed by Wijma et al. (1998) to measure the fear of childbirth experienced by women after childbirth. The scale consists of 32 items. Responses are numbered from 0 to 5 and are a six-point Likert-type scale. 0 represents "completely," and 5 represents "not at all." The minimum score on the scale is 0, while the maximum score is 160.

    first 24 hours after birth

  • Depression Anxiety Stress Scale-21

    The Depression Anxiety Stress Scale-21 was developed by Lovibond and Lovibond (1995), and its Turkish validity and reliability study was conducted by Sarıçam (2018). The scale consists of 21 items, with 7 items each in the depression, anxiety, and stress subscales. It assesses depression, anxiety, and stress symptoms in the past week on a four-point scale from (0) never to (3) always. A score of 5 or higher on the depression subscale, 4 or higher on the anxiety subscale, and 8 or higher on the stress subscale indicates a relevant problem.

    In the 28th week of pregnancy, After completing the program (4 weeks), 1st month postpartum, 3rd month postpartum

Study Arms (2)

Control group

NO INTERVENTION

A self-compassion based birth preparation program group

EXPERIMENTAL

A self-compassion based birth preparation program

Other: A self-compassion based birth preparation program

Interventions

A self-compassion based birth preparation program

A self-compassion based birth preparation program group

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Those who are 18 years of age and older,
  • Those who have at least primary school education,
  • Those who understand and speak Turkish,
  • Those who reside within the borders of Ordu province,
  • Those who have no obstacle to vaginal birth,
  • Those who conceive naturally,
  • Those who have a singleton pregnancy,
  • Those who are 28 weeks or more pregnant,
  • Pregnant women who agree to participate in the study will be included.

You may not qualify if:

  • \- Those who have a history of risky pregnancies,
  • Those who have chronic and/or psychiatric health problems,
  • Those who are planned for a cesarean section due to medical indications at any stage of the study,
  • Those who do not attend at least three sessions of the education program,
  • Those who are at risk during the pregnancy at any stage of the study,
  • Pregnant women who start labor while the study is ongoing will be excluded from the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ordu University

Ordu, Ordu, 52000, Turkey (Türkiye)

Location

Related Links

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Model Details: There is an intervention and control group.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Research Assistant

Study Record Dates

First Submitted

June 11, 2025

First Posted

September 23, 2025

Study Start

September 24, 2025

Primary Completion (Estimated)

June 12, 2026

Study Completion (Estimated)

June 20, 2026

Last Updated

November 18, 2025

Record last verified: 2025-11

Data Sharing

IPD Sharing
Will not share

Locations