- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07332065
The Effects of Mandala Coloring on Women During Menopause
May 8, 2026 updated by: Kevser Katkaya, Kahramanmaras Sutcu Imam University
The Effect of Mandala Coloring on Menopausal Symptoms, Sexual Quality of Life, and Self-Esteem in Women During the Menopause Period
The aim of this clinical study is to determine the effect of mandala coloring on menopausal symptoms, sexual quality of life, and self-esteem in women during menopause period. The main questions the study aims to answer are as follows:
- Does mandala coloring reduce the severity of menopausal symptoms in women?
- Is there an increase in self-esteem levels among women who participate in mandala coloring after the intervention?
- Is there an increase in the quality of sexual life among women who participate in mandala coloring after the intervention? Researchers will compare the intervention group (those who participated in mandala coloring) with the control group (those who did not participate in any intervention) to evaluate the effectiveness of mandala coloring.
Participants
- Participants in the intervention group will attend 30-minute mandala coloring sessions once a week for 4 weeks.
- Participants in the control group will not receive any intervention during the same period.
- Both groups will be assessed using a questionnaire at the beginning of the study and at the end of the 4th week (pre-test/post-test).
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Menopause is a natural, biological process that marks the end of a woman's fertile years.
Every woman's menopause is unique.
The experience, severity, duration, and physical and psychological effects of menopause are all unique.
During this period, women must contend with both the processes of aging and the hormonal changes that occur during menopause.
These changes can sometimes negatively impact an individual's life, reducing their quality of life.
Menopausal symptoms can often appear one to two years before their last menstrual period and up to 15 years afterward.
These symptoms, such as decreased sexual desire, decreased estrogen levels, mood disorders, illnesses associated with menstruation, decreased genital sensation, vaginal dryness, physical discomfort, and bone loss, can lead to a loss of sexual desire and alienate a person from their partner.
This, in turn, leads to a decrease in self-esteem, a feeling of unease about one's own characteristics and ongoing physical and psychological changes.
Consequently, individuals' anxiety levels increase, and their ability to cope with symptoms decreases.
Studies have highlighted the benefits of alternative methods for coping with anxiety in women undergoing menopause.
Music therapy and art therapy are examples.
Studies have also demonstrated the therapeutic effects of mandala coloring, an art therapy activity.
This study aims to examine the effects of mandala coloring on menopausal symptoms, quality of sexual life, and self-esteem in menopausal women.
Study Type
Interventional
Enrollment (Actual)
70
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 Locations
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Kahramanmaraş, Turkey (Türkiye), 46050
- Saçaklızade Family Health Center No. 30
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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
No
Description
Inclusion Criteria:
- Being between the ages of 40 and 65,
- Not having experienced menstruation for at least one year,
- Having a score of 15 or higher on the MSDS (meaning having experienced at least moderate menopause),
- Not having received hormone replacement therapy for menopausal symptoms,
- Not having undergone surgical menopause,
- Experiencing at least one vasomotor symptom of menopause (hot flashes, night sweats, sudden sweating attacks, palpitations, chills and shivering attacks, etc.).
- Being able to read, write, speak, and understand Turkish,
- Not having previously received mandala art therapy training or regularly practicing mandala coloring,
- Not having an allergy to mandala coloring materials,
- Not practicing spiritual practices such as yoga or meditation,
- Agreeing to participate in the study.
Exclusion Criteria:
- Having a physical symptom that may prevent mandala coloring,
- Having communication and perception problems,
- Having difficulty understanding or speaking Turkish,
- Having a psychiatric illness or taking psychiatric medication,
- Having experienced a loss in the last 6 months.
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: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Mandala coloring
Participants will take part in 30-minute mandala painting sessions once a week for four weeks.
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Mandala coloring is a structured creative art activity based on colouring mandala shapes, which consist of circular and symmetrical patterns, increasing focus and promoting relaxation.
As one of the art therapies, mandala colouring can have a therapeutic effect on individuals.
Other Names:
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No Intervention: Control group
No intervention will be applied to participants in the control group within 4 weeks.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Menopausal Symptoms
Time Frame: Time Frame: Fromenrollmenttotheend of intervention at 4 weeks.
|
The primary outcome measure in this study is the severity of menopausal symptoms as assessed by the Menopause Rating Scale.
This scale is an 11-item measure developed by Heineman et al. (1996) to assess the severity of menopausal symptoms.
The minimum score that can be obtained on the scale is 0, while the maximum score is 44.
An increase in the score obtained from the scale indicates an increase in the severity of the complaints experienced, while also showing that quality of life has been negatively affected.
In this study, the validity and reliability of the scale in Turkish were conducted by Can Gürkan (2005).
The Turkish version of the scale will be used.
Within the scope of the current study, it is expected that women in menopause who engage in mandala coloring will show improvement in menopause symptoms.
In other words, the Menopause Rating Scale scores of women in the experimental group will be lower than those of women who do not practice mandala coloring.
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Time Frame: Fromenrollmenttotheend of intervention at 4 weeks.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Sexual Quality Of Life
Time Frame: Time Frame: From enrollment to the end of intervention at 4 weeks.
|
In this study, the secondary outcome measure is the level of sexual quality of life assessed using the Sexual Quality of Life Scale.
The scale, developed by Symonds et al. (2005), consists of 18 items designed to measure women's sexual quality of life.
Participants are expected to respond to the items based on their sexual life over the past four weeks.
The lowest possible score on the scale is 18, and the highest possible score is 108.
A higher score on the scale indicates a better quality of sexual life.
The Sexual Quality of Life Scale - Female Turkish Form will be used in this study.
Its validity and reliability in Turkish were conducted by Gölbaşı (2010).
Within the scope of the current study, it is expected that women in menopause who practice mandala coloring will show an increase in their sexual life quality.
In other words, the Sexual Life Quality Scale scores of the women in the experimental group are higher than those of women who do not practice mandala coloring.
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Time Frame: From enrollment to the end of intervention at 4 weeks.
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Self-Esteem
Time Frame: Time Frame: From enrollment to the end of intervention at 4 weeks.
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Another secondary outcome measure in this study is the level of self-esteem, assessed using the Coopersmith Self-Esteem Inventory Scale.
The scale was developed by Stanley Coopersmith (1967).
It consists of 25 items with opposite responses such as "Like me" or "Not like me."
The content includes the person's outlook on life, family relationships, social relationships, and resilience.
The lowest possible score on the scale is 0, and the highest is 25.
A low score on the scale indicates low self-esteem, while a high score indicates high self-esteem.
Turkish reliability and validity studies were conducted by Aksoy (1992) and Pişkin (1997).
Within the scope of the study, it is expected that women in menopause who practice mandala coloring will experience an increase in their self-esteem levels.
In other words, the scores obtained by the women in the experimental group on the Coopersmith Self-Esteem Inventory Scale are higher than those of women who do not practice mandala coloring.
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Time Frame: From enrollment to the end of intervention at 4 weeks.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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 (Actual)
January 25, 2026
Primary Completion (Actual)
February 25, 2026
Study Completion (Actual)
March 25, 2026
Study Registration Dates
First Submitted
December 11, 2025
First Submitted That Met QC Criteria
December 31, 2025
First Posted (Actual)
January 12, 2026
Study Record Updates
Last Update Posted (Actual)
May 11, 2026
Last Update Submitted That Met QC Criteria
May 8, 2026
Last Verified
May 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- KahramanmaraşSIU-NURSİNG-KK-01
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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