- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07470632
Effect of Twin Hearts Meditation and Mandala Coloring on Exam Anxiety in Nursing Students (Mandala)
Comparison of Mandala Coloring and Twin Hearts Meditation on Practical Exam Anxiety: A Randomized Clinical Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Purpose
The purpose of this study was to compare the effectiveness of Mandala coloring and Twin Hearts Meditation as complementary and non-pharmacological interventions for reducing exam anxiety among undergraduate nursing students.
Study Design
This study was designed as a randomized clinical trial conducted among undergraduate nursing students. Participants were randomly assigned to two intervention groups: Mandala coloring and Twin Hearts Meditation.
Sample Size
Out of 110 eligible nursing students, 100 who met the inclusion criteria were recruited. Based on previous research and a mean comparison formula with a significance level of 0.05 and a statistical power of 80%, the required sample size was calculated as 48 participants per group. Considering possible dropout, 50 participants were included in each group.
Data Collection Tools
Data were collected using:
- A demographic questionnaire (age, gender, marital status, academic information)
- The State-Trait Anxiety Inventory (STAI), a validated 40-item self-report instrument measuring state and trait anxiety.
Intervention
Participants were randomly assigned to one of two groups:
Twin Hearts Meditation Group:
Participants received a guided Twin Hearts Meditation session lasting 30 minutes under the supervision of the researcher.
Mandala Coloring Group:
Participants engaged in mandala coloring for 30 minutes using printed mandala designs and colored pencils under the supervision of the researcher.
Both interventions were conducted before a practical examination.
Outcome Assessment
Anxiety levels were measured before and after the intervention using the State-Trait Anxiety Inventory (STAI).
Ethical Considerations
The research received approval from the Cyprus International University Ethics Review Board (Approval No: EKK23-24/012/07). The study followed the ethical standards of the Council of Ethics and adhered to the principles of the Declaration of Helsinki (1964).
Statistical Analysis
Data were analyzed using SPSS software. Descriptive statistics, paired t-tests, independent t-tests, and chi-square tests were used. A P value < 0.05 was considered statistically significant.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
North Cyprus
-
Nicosia, North Cyprus, Cyprus
- KKTC (Turkish Republic Of Northern Cyprus)
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- All undergraduate nursing students in their first semester, male or female, enrolled in the English-language nursing program.
- Students not using other stress-reduction methods (e.g., progressive muscle relaxation, pharmacological therapy).
- Students who voluntarily agreed to participate and provided informed consent.
Exclusion Criteria:
- Unwilling to continue cooperation in the project.
- Using any psycho medicines (anti-depressants ...), mental health.
- Mourning, especially the death of loved ones or relatives in the 1st phase.
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 |
|---|---|
|
Experimental: Twin Hearts Meditation
Behavioral: Twin Heart Meditation Participants in this group receive the Twin Heart Meditation intervention, a guided meditative technique based on the principles of loving-kindness and spiritual energy.
The intervention is designed to reduce exam-related anxiety by promoting inner peace and emotional regulation.
|
Participants in this group receive Twin Hearts Meditation, a guided meditation technique based on the principles of loving-kindness and spiritual energy. The intervention aims to reduce exam-related anxiety by promoting emotional balance and relaxation. Intervention: Behavioral: Twin Hearts Meditation Participants practice guided meditation sessions lasting 30 minutes under the supervision of the researcher. The meditation protocol includes: Physical warm-up exercises Activation of the heart chakra Activation of the crown chakra Blessing the Earth with loving-kindness Silent meditation using the phrase "Amen" Expression of gratitude Closing exercises Sessions are conducted in a quiet room using audio guidance.
Participants were provided with a printed mandala outline on A4 paper and six colored pencils (red, orange, yellow, green, blue, purple).
They engaged in free, unstructured mandala coloring for 30 minutes
|
|
Experimental: Mandala Coloring
Participants in this group engage in mandala coloring, an art-based mindfulness activity designed to reduce exam anxiety and promote relaxation.
|
Participants in this group receive Twin Hearts Meditation, a guided meditation technique based on the principles of loving-kindness and spiritual energy. The intervention aims to reduce exam-related anxiety by promoting emotional balance and relaxation. Intervention: Behavioral: Twin Hearts Meditation Participants practice guided meditation sessions lasting 30 minutes under the supervision of the researcher. The meditation protocol includes: Physical warm-up exercises Activation of the heart chakra Activation of the crown chakra Blessing the Earth with loving-kindness Silent meditation using the phrase "Amen" Expression of gratitude Closing exercises Sessions are conducted in a quiet room using audio guidance.
Participants were provided with a printed mandala outline on A4 paper and six colored pencils (red, orange, yellow, green, blue, purple).
They engaged in free, unstructured mandala coloring for 30 minutes
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Exam Anxiety Levels
Time Frame: Anxiety levels are assessed at two time points: before the intervention (two hours prior to the OSCE) and immediately after the intervention prior to the examination.
|
The primary outcome measure evaluates changes in exam-related anxiety levels among nursing students following the Mandala coloring and Twin Hearts Meditation interventions. Anxiety is measured using the State-Trait Anxiety Inventory (STAI), a validated psychological instrument that assesses both state and trait anxiety. The STAI consists of two subscales with 20 items each, scored on a 4-point Likert scale. Higher scores indicate greater levels of anxiety. Both groups completed the State-Trait Anxiety Inventory (STAI) two hours before the Objective Structured Clinical Examination (OSCE), immediately prior to the intervention, and again immediately after the intervention. |
Anxiety levels are assessed at two time points: before the intervention (two hours prior to the OSCE) and immediately after the intervention prior to the examination.
|
|
Test Anxiety Levels
Time Frame: Anxiety levels are assessed at two time points: before the intervention (two hours prior to the OSCE) and immediately after the intervention prior to the examination.
|
The primary outcome measure evaluates changes in exam-related anxiety levels among nursing students following the Mandala coloring and Twin Hearts Meditation interventions. Anxiety is measured using the State-Trait Anxiety Inventory (STAI), a validated psychological instrument that assesses both state and trait anxiety. The STAI consists of two subscales with 20 items each, scored on a 4-point Likert scale. Higher scores indicate greater levels of anxiety. Both groups completed the State-Trait Anxiety Inventory (STAI) two hours before the Objective Structured Clinical Examination (OSCE), immediately prior to the intervention, and again immediately after the intervention. |
Anxiety levels are assessed at two time points: before the intervention (two hours prior to the OSCE) and immediately after the intervention prior to the examination.
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Pouran Varvani Farahani, PhD, PhD in Pediatric Nursing, Department of Nursing, Faculty of Health Science, Cyprus International 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
Other Study ID Numbers
- PVF2026Mandalamed
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
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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