- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05534867
Effects of Mandala Coloring on Anxiety in Pregnant Women
Effects of Mandala Coloring on Anxiety in Pregnant Women: Randomized Controlled Experimental Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Pregnancy is an important period in a woman's life in which she experiences different spiritual, physical and emotional experiences. While experiencing this process, women may face many factors that may affect their mental health, such as stress, anxiety and depression. When the literature is examined, it is stated that approximately 10% to 24.2% of pregnant women experience anxiety or stress during their pregnancy.It is very important to diagnose it in the early stages of pregnancy, as anxiety in pregnancy can have negative effects on maternal and newborn health, especially in the birth and postpartum period.
A number of alternatives have been found to reduce anxiety, one of which is using it in the form of art therapy.In the opinion of art psychotherapists, mandala painting is one of the main tools of other art psychotherapy techniques that focus on healing.A number of studies have been conducted to determine the effect of drawing or coloring a mandala on anxiety.
Amelia et al conducted research that proved that drawing and coloring mandalas effectively reduces students' anxiety levels. In Turkey, a study was conducted by Sezen and Ünsalver on the fear of childbirth in pregnant women, including art therapy. In the study, 7 types of art therapy were applied to the women, including listening to music and singing, making masks, drawing, making mandalas, making dolls, taking photographs and making collages. As a result of the research, it was determined that art therapy was effective in reducing anxiety.
When the studies are examined, there are studies on the application of mandala to reduce the anxiety felt by children in cancer patients, but there are no studies on reducing pregnancy-related anxiety of women during pregnancy. This research was planned as a randomized controlled experimental study in order to reduce the anxiety felt by expectant mothers in relation to pregnancy during pregnancy.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Adana, Turkey
- Çukurova University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Ability to read and understand Turkish
- Being between the ages of 20-35,
- Single pregnancy
- Don't be primiparous
- Having 40 or more from STAI
- Volunteering to participate in the research
- Fully answering survey and scale forms.
- Being in the first, 2nd or 3rd trimester
Exclusion Criteria:
- Having been diagnosed with a risky pregnancy
- Unwilling to continue working
- Having a chronic disease (Diabetes, Hypertension, Thyroid etc.),
- Having any problem that prevents communication (such as hearing, speaking, and understanding abilities),
- Using one of the pharmacological or non-pharmacological methods to reduce anxiety and receiving psychiatric treatment (Pharmacotherapy or psychotherapy).
- Lack of a smart phone and internet
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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No Intervention: Control group
Participants in this group will consist of people who do not routinely do any practice on their own to reduce anxiety symptoms.
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Experimental: Mandala coloring group
Mandala painting will be applied to pregnant women who have anxiety related to pregnancy.
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Participants will be asked to choose the pages they want from 12 colored felt-tip pen paint sets and 16 mandala coloring pages given to each participant by the researcher for 1 month, 2 days a week, at any time of the day and for an average of 20-30 minutes each time, and paint them in the colors they want.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Introductory Information form
Time Frame: between one to six months
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A form that includes questions about women's socio-demographic and pregnancy and characteristics.
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between one to six months
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the Spielberger State-Trait Anxiety Inventory (STAI) scale
Time Frame: between one to six months
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This scale, developed by Spielberg in 1973, consists of 20 questions.
It is a 4-point Likert type scale (1=not at all, 4=very much).
The lowest score that can be obtained from the scale is 20, and the highest score is 80.
The higher the score is, the higher the anxiety level is.
The alpha value of the scale is 0.86-.92.33.
The validity and reliability study in our country was conducted by Oner et al., in 1983 and the alpha value was found between.
The scale that will be used to evaluate the state and trait anxiety of pregnant women.
As the score increases, it is determined that the anxiety is higher.
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between one to six months
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Pregnancy-related anxiety scale
Time Frame: between one to six months
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This scale was developed by Brunton, whose validity and reliability in Turkish were made by Şolt and Gül.
As the score obtained from the scale increases, the level of pregnancy-related anxiety increases.
It will be used to assess pregnancy-related anxiety.
As the score obtained in the scale consisting of 9 sub-dimensions increases, it is determined that the anxiety of the pregnant woman is also higher.
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between one to six months
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Director: AYCA SOLT KIRCA, Phd, Kırklareli University
- Principal Investigator: Elif Dağlı, Phd, Çukurova University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KırklareliAS-6
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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