- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07448636
The Effect of Postpartum Mandala Coloring on Anxiety, Fatigue, Maternal Attachment and Breastfeeding Self-efficacy
February 26, 2026 updated by: DİDEM KAYA, Nuh Naci Yazgan University
The Effect of Mandala Coloring on Anxiety, Fatigue, Maternal Attachment, and Breastfeeding Self-Efficacy in the Postpartum Period: A Randomized Controlled Experimental Study
The aim of this study is to investigate the effects of mandala coloring on anxiety, fatigue, breastfeeding self-efficacy, and mother-infant bonding in postpartum mothers.
The sample consists of women who have had a cesarean section at Kayseri City Hospital within the last year.
Data will be collected using a Personal Information Form, the Postpartum Specific Anxiety Scale, the Short Form of the Breastfeeding Self-Efficacy Scale, the Chalder Fatigue Scale, and the Maternal Attachment Scale.
Mothers meeting the inclusion criteria will be randomly assigned to intervention and control groups.
Mothers in the intervention group will be informed that they will begin mandala coloring one week after their cesarean delivery.
They will be asked to color a mandala twice a week for a total of 5 weeks, with each coloring session lasting 30 minutes.
To eliminate the possibility of mothers forgetting to color the mandala, the researcher will send reminder messages twice a week starting from the end of the first week.
The Personal Information Form will be collected through face-to-face interviews while the mothers are in the hospital.
Mothers in the control group will receive routine hospital care and will not paint mandalas.
Researchers will call all mothers at the end of weeks 1 and 2 to administer the Postpartum Specific Anxiety Scale and the Short Form of the Breastfeeding Self-Efficacy Scale, and at the end of weeks 4 and 6 to administer questions from the Postpartum Specific Anxiety Scale, Short Form of the Breastfeeding Self-Efficacy Scale, Chalder Fatigue Scale, and Maternal Attachment Scale, recording their responses.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Detailed Description
The postpartum period is a time of physiological changes as well as the assumption of new roles and responsibilities.
Postpartum anxiety has been relatively neglected in recent years.
Defined as a condition that causes anxiety and depression of unknown origin, anxiety is seen as a normal reaction to the birth of a new baby in the postpartum period.
Clinically, the prevalence of anxiety symptoms in the postpartum period ranges from 12-20%.
High levels of anxiety negatively affect the bonding between mother and baby, as well as the baby's behavioral, social, and emotional development.
Postpartum fatigue causes women to feel more negative and less competent than usual.
Postpartum fatigue negatively impacts the mother's functional recovery, maternal behavior, infant care, relationships with family members, work performance, and self-actualization.
While fatigue is common and even expected after childbirth, severe postpartum fatigue can have significant effects on women's health and activities; It has negative effects such as deterioration of maternal health, delayed return to daily life activities, early cessation of breastfeeding, and delayed infant development.
Since cesarean delivery is a surgical procedure, postpartum fatigue, pain, and anxiety are higher compared to vaginal delivery.
Consequently, the time to start breastfeeding is later, especially in the first 24 hours after cesarean delivery, mothers have lower breastfeeding self-efficacy, and their need for support from healthcare personnel is higher.
Art therapy is reported as an effective support method that addresses the physical, mental, social, and emotional aspects of the individual and helps in coping with difficulties.
Mandala, one of the art therapy methods, is defined as a method used to transfer emotions and thoughts onto paper, usually in a round shape.
Studies conducted on different sample groups have found that mandala painting is effective on anxiety and fatigue.
A literature review revealed that anxiety and fatigue are common in the postpartum period, negatively impacting breastfeeding self-efficacy and maternal attachment.
Studies have also shown that mandala coloring is effective in reducing anxiety and fatigue.
However, the effects of mandala coloring on mothers' anxiety, fatigue, breastfeeding self-efficacy, and maternal attachment in the postpartum period have not been investigated.
The aim of this study is to investigate the effects of mandala coloring on anxiety, fatigue, breastfeeding self-efficacy, and maternal attachment in mothers in the postpartum period.
Study Type
Interventional
Enrollment (Estimated)
140
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Didem Kaya, Assistant Professor Doctor
- Phone Number: +905343035254
- Email: didemkaya86@gmail.com
Study Locations
-
-
Kayseri
-
Kayseri, Kayseri, Turkey (Türkiye)
- Nuh Naci Yazgan University
-
Contact:
- Didem Kaya, Assistant Professor Doctor
- Phone Number: +905343035254
- Email: didemkaya86@gmail.com
-
Principal Investigator:
- Didem Kaya, Assistant Professor Doctor
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Being 18 years of age or older
- Having had a cesarean delivery after the 37th week of gestation
- The baby being with the mother and the mother being able to breastfeed
- Volunteering to participate in the study
- Having a planned cesarean section
Exclusion Criteria:
- The mother is currently or has previously received psychiatric treatment.
- The mother has a physical disability in her upper extremities.
- The mother has a vision problem.
- The newborn has a congenital anomaly.
- The newborn experienced an obstetric complication requiring immediate hospitalization after birth (hemorrhage, infection, bladder damage, preeclampsia, etc.).
Criteria for terminating the study:
- The baby or mother has a medical condition requiring hospitalization within 6 weeks postpartum.
- Communication with the mother is not possible within 6 weeks postpartum
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mandala Coloring Group
Mothers in this group will color mandalas.
|
Mothers in the intervention group will be given a circular mandala template coloring book and 12 colored pencils.
Mothers in the intervention group will be informed that they will start coloring mandalas one week after giving birth.
They will be asked to color one mandala coloring page twice a week for a total of 5 weeks, with each coloring session lasting 30 minutes.
To eliminate the possibility of mothers forgetting to color mandalas, the researcher will send reminder messages to the mothers twice a week starting from the end of the first week.
Mothers will be asked to send pictures of the mandala pages they have colored to the researcher as a message.
|
|
No Intervention: Control Group
Mothers in this group will not color mandalas.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Postpartum Specific Anxiety Scale
Time Frame: At the end of the 1st, 2nd, 4th and 6th weeks postpartum
|
The scale was developed by Fallon et al. (2016) as a 56-item scale, and was transformed into a 44-item structure through a Turkish validity and reliability study conducted by Bayri Bingöl et al. (2021).
The original version of the scale was developed and validated with mothers who had infants aged 0-6 months.
The scale has sub-dimensions of maternal skills and attachment, newborn well-being and safety, infant care practices, and psychosocial adjustment to motherhood.
The highest possible score on the Likert-type scale is 176, and the cutoff score is 113.5.
Higher scores on the scale indicate a higher incidence of anxiety symptoms.
The Cronbach's alpha values for the sub-dimensions of the scale range from 0.83 to 0.90.
|
At the end of the 1st, 2nd, 4th and 6th weeks postpartum
|
|
Short Form of the Breastfeeding Self-Efficacy Scale
Time Frame: At the end of the 1st, 2nd, 4th and 6th weeks postpartum
|
Developed in 1999 by Dennis and Faux to measure mothers' competence regarding breastfeeding in the postpartum period.
The scale was initially developed with 33 items.
In the internal consistency analysis of the scale, items with a correlation below 0.60 were removed, and the short form of the Breastfeeding Self-Efficacy Scale with 14 items was created.
This scale is a 5-point Likert type.
All items are scored as 1, 2, 3, 4, 5 (1=Never sure, 5=Always sure).
All items in the scale have positive meanings.
The lowest possible score on the scale is 14, and the highest is 70, with no cutoff point.
A higher score indicates higher breastfeeding self-efficacy.
The Turkish validity and reliability of the scale was established by Aluş-Tokat and Okumuş in 2010.
The Cronbach's alpha coefficient of the Breastfeeding Self-Efficacy Scale is 0.86.
|
At the end of the 1st, 2nd, 4th and 6th weeks postpartum
|
|
Chalder Fatigue Scale
Time Frame: At the end of the 4th and 6th weeks postpartum
|
Developed by Cella and Chalder in 2010 for use in various populations to assess fatigue, it was adapted into Turkish by Adın et al. in 2022.
The scale consists of 11 items, divided into two sub-dimensions: physical fatigue and mental fatigue, and uses a 4-point Likert scale.
Scores range from 0-21 for the physical fatigue sub-dimension, 0-12 for the mental fatigue sub-dimension, and 0-33 for the total scale score.
Higher scores indicate greater fatigue severity.
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At the end of the 4th and 6th weeks postpartum
|
|
Maternal Attachment Scale
Time Frame: At the end of the 4th and 6th weeks postpartum
|
The validity and reliability study of the Turkish form of the Maternal Attachment Scale, developed by Mary E. Muller in 1994, was conducted by Kavlak and Şirin in 2009.
The scale consists of 26 items on a four-point Likert scale, with higher scores indicating higher maternal attachment.
The lowest possible score is 26, and the highest is 104.
Cronbach's Alpha internal consistency reliability was found to be 0.77 in 1-month-old infants and 0.82 in 4-month-old infants.
|
At the end of the 4th and 6th weeks postpartum
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
March 15, 2026
Primary Completion (Estimated)
May 20, 2026
Study Completion (Estimated)
December 31, 2026
Study Registration Dates
First Submitted
February 26, 2026
First Submitted That Met QC Criteria
February 26, 2026
First Posted (Actual)
March 4, 2026
Study Record Updates
Last Update Posted (Actual)
March 4, 2026
Last Update Submitted That Met QC Criteria
February 26, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- NuhNaciYazganUdk1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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