Postpartum Effects of Mirror Therapy During Labor
"Recognize Your Strength: The Effects of Mirror Therapy Applied During Labor on Postpartum Pain, Mood, and Emotional Well-Being: A Randomized Controlled Trial"
1 other identifier
interventional
86
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2026
Shorter than P25 for not_applicable
1 active site
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 Start
First participant enrolled
August 1, 2026
CompletedFirst Submitted
Initial submission to the registry
August 24, 2026
CompletedFirst Posted
Study publicly available on registry
August 28, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 30, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
February 27, 2027
August 28, 2026
August 1, 2026
3 months
August 24, 2026
August 26, 2026
Conditions
Keywords
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
EXPERIMENTALMirror Therapy Application
2 control
NO INTERVENTIONRoutine Care
Interventions
Eligibility Criteria
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
- NURTEN ÖZÇALKAPlead
Study Sites (1)
Ağrı İbrahim Çeçen University
Ağrı, Ağri, 04100, Turkey (Türkiye)
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
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
BÜŞRA YAĞLU, Midwife
- STUDY DIRECTOR
Nurten OZCALKAP, asisst. prof
Agri Ibrahim Cecen University
- STUDY CHAIR
Gizem Barakanlı, Midwife
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