NCT07792629

Brief Summary

Today, childbirth is considered one of the most physically and psychologically intense experiences in a woman's life. Labor is a critical period during which fear, anxiety, and stress related to childbirth may increase, potentially affecting both the course of labor and postpartum emotional well-being. Supportive approaches implemented during this period may contribute to a more positive perception of the childbirth experience and enhance postpartum well-being. Mirror therapy is a non-pharmacological approach that enables individuals to visually perceive their own bodies and the ongoing process, thereby strengthening self-perception and promoting positive body awareness. The use of mirror therapy during labor may increase women's active participation in the childbirth process and enhance their sense of control. It may also support emotional well-being and reduce negative emotional states during the postpartum period. Accordingly, this study aims to evaluate the effects of mirror therapy administered during labor on postpartum pain, mood, and emotional well-being. The findings are expected to contribute to strengthening midwifery support during childbirth, integrating non-pharmacological approaches into clinical practice, promoting their wider use, and protecting women's psychological well-being. Thus, the study is expected to provide scientific evidence that may inform midwifery education and practice as well as postpartum care policies.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
86

participants targeted

Target at P50-P75 for not_applicable

Timeline
6mo left

Started Aug 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress14%
Aug 2026Feb 2027

Study Start

First participant enrolled

August 1, 2026

Completed
23 days until next milestone

First Submitted

Initial submission to the registry

August 24, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

August 28, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2026

Expected
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 27, 2027

Last Updated

August 28, 2026

Status Verified

August 1, 2026

Enrollment Period

3 months

First QC Date

August 24, 2026

Last Update Submit

August 26, 2026

Conditions

Keywords

Mirror Therapy,Childbirth,Mood,Postpartum

Outcome Measures

Primary Outcomes (3)

  • Descriptive Information Form:

    This form was developed by the researchers and includes questions regarding the participants' demographic and obstetric characteristics.

    baseline

  • Emotional Well-Being Scale: Baseline (before the intervention)

    The Psychological Well-Being Scale was developed by Diener et al. (2010) and adapted into Turkish by Telef (2013). The scale consists of eight items within a single-factor structure and is rated on a 7-point Likert-type scale ranging from 1 to 7. The single-factor structure explains 42% of the total variance, with factor loadings ranging from .54 to .76. The Cronbach's alpha reliability coefficient of the scale was reported as .80 (Telef, 2013, p. 381).

    Baseline (before the intervention), Immediately after the intervention

  • Visual Analog Scale (VAS):

    The Visual Analog Scale is a unidimensional instrument used to assess the participant's perceived pain intensity by converting a subjective experience into a quantitative value. The VAS consists of a 100-mm (10-cm) horizontal line, with one endpoint representing "no pain" (0) and the other representing the "worst possible pain" (10). Participants are asked to mark the point on the line that best represents the intensity of their current pain. The distance between the "no pain" endpoint and the participant's mark is measured using a ruler and recorded in centimeters, with higher scores indicating greater pain intensity. VAS scores are interpreted according to the predefined pain-intensity categories used in the study (Ergin, 2013; Aslan, 2006; Mucuk, 2009).

    Baseline (before the intervention), Immediately after the intervention

Study Arms (2)

1 Mirror Therapy

EXPERIMENTAL

Mirror Therapy Application

Other: Mirror Therapy

2 control

NO INTERVENTION

Routine Care

Interventions

Mirror Therapy Application

1 Mirror Therapy

Eligibility Criteria

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

You may qualify if:

  • Women aged 18 years or older,
  • Able to read and write in Turkish,
  • Admitted for vaginal delivery,
  • Willing to participate voluntarily in the study,
  • Providing written informed consent by signing the "Informed Voluntary Consent Form."

You may not qualify if:

  • Having difficulty communicating,
  • Having a high-risk pregnancy (e.g., hypertension, diabetes),
  • Experiencing complications during labor or delivery (e.g., emergency cesarean section, fetal distress).

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Ağrı İbrahim Çeçen University

Ağrı, Ağri, 04100, Turkey (Türkiye)

RECRUITING

Related Publications (1)

  • • Diener, E., Wirtz, D., Tov, W., Kim-Prieto, C., Choi, D., Oishi, S., & Biswas-Diener, R. (2009). New measures of well-being: Flourishing and positive and negative feelings. Social Indicators Research, 97(2), 143-156.

    RESULT

Related Links

MeSH Terms

Interventions

Mirror Movement Therapy

Intervention Hierarchy (Ancestors)

Physical Therapy ModalitiesRehabilitationTherapeutics

Study Officials

  • BÜŞRA YAĞLU, Midwife

    PRINCIPAL INVESTIGATOR
  • Nurten OZCALKAP, asisst. prof

    Agri Ibrahim Cecen University

    STUDY DIRECTOR
  • Gizem Barakanlı, Midwife

    STUDY CHAIR

Central Study Contacts

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Asisst. prof

Study Record Dates

First Submitted

August 24, 2026

First Posted

August 28, 2026

Study Start

August 1, 2026

Primary Completion (Estimated)

October 30, 2026

Study Completion (Estimated)

February 27, 2027

Last Updated

August 28, 2026

Record last verified: 2026-08

Data Sharing

IPD Sharing
Will not share

Locations