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Effect of Mandala Coloring on Menopausal Attitude, Perceived Stress and Mindfulness

The Effect of Mandala Coloring on Menopausal Attitudes, Perceived Stress, and Mindfulness in Women During Menopause: A Randomized Controlled Trial

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07657429
Acronym
MANDALA-MENO
Enrollment
140
Registered
2026-06-18
Start date
2026-05-30
Completion date
2026-09-30
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Menopause, Mindfulness, Psychological Stress

Keywords

Mandala Coloring, Menopause, Perceived Stress, Mindfulness, Women Health, Randomized Controlled Trial

Brief summary

Menopause is a natural life stage associated with hormonal changes that may affect women physically and psychologically. During this period, women may experience increased stress levels, negative attitudes toward menopause, and decreased mindfulness. Mandala coloring is a structured art-based intervention that may promote relaxation and improve psychological well-being. This randomized controlled trial aims to evaluate the effect of mandala coloring on attitudes toward menopause, perceived stress, and mindfulness levels among menopausal women.

Detailed description

Menopause is a natural stage of life characterized by hormonal changes that may affect women's physical and psychological well-being. During this period, women may experience vasomotor symptoms, sleep disturbances, mood changes, increased stress, and negative attitudes toward menopause. Supporting women's psychological well-being during menopause has become an important aspect of women's health care.Mindfulness-based and art-based interventions have increasingly been used as non-pharmacological approaches to improve psychological health and reduce stress. Mandala coloring is a structured art-based intervention that promotes concentration, helps individuals focus on the present moment, and may contribute to emotional regulation and relaxation. Previous studies have shown that mandala coloring may reduce anxiety and stress levels while improving overall well-being.This study will be conducted as a parallel-group randomized controlled experimental trial. The study will take place at Islampasa Family Health Center No.12 located in Rize, Türkiye. A total of 140 menopausal women aged between 45 and 55 years who meet the eligibility criteria will be included in the study.Participants will be randomly assigned to either an intervention group or a control group using a web-based randomization procedure. Women assigned to the intervention group will participate in structured mandala coloring sessions for four weeks, three times per week, for a total of 12 sessions. The first session will be conducted face-to-face at the family health center under researcher supervision. The remaining sessions will be completed individually by participants at home during evening hours.Participants in the control group will receive routine care provided at the family health center without any additional intervention.Data will be collected before and after the intervention using the Personal Information Form, Menopause Attitude Scale, Perceived Stress Scale, and State Mindfulness Scale.The primary purpose of this study is to determine whether structured mandala coloring has an effect on attitudes toward menopause, perceived stress, and mindfulness levels in menopausal women.

Interventions

BEHAVIORALMandala Coloring Program

Participants in the intervention group will receive a mandala coloring program for 4 weeks. The program will be performed 3 times per week, for a total of 12 sessions. The first session will be conducted face-to-face at the family health center, and the remaining sessions will be completed at home. Participants will use standardized mandala templates and coloring materials provided by the researchers.

OTHERRoutine Care

Participants in the control group will receive routine care provided by the family health center. This includes general health monitoring, menopausal health counseling, and standard follow-up services without any mandala coloring intervention during the study period.

Sponsors

Ondokuz Mayıs University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Participants will be randomly assigned to either the mandala coloring intervention group or the routine care control group in parallel.

Eligibility

Sex/Gender
FEMALE
Age
45 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Inclusion Criteria: * Women aged 45-55 years * Being in the menopausal period (absence of menstruation for at least 12 months) * Ability to read and understand Turkish * Voluntary agreement to participate in the study *

Exclusion criteria

* Diagnosed psychiatric or cognitive disorders * Communication problems preventing participation * Visual impairment or fine motor limitations preventing mandala coloring * Use of hormone replacement therapy * Regular participation in mandala coloring, mindfulness, or similar mind-body practices

Design outcomes

Primary

MeasureTime frameDescription
Perceived Stress LevelBaseline and 4 weeks after interventionChanges in perceived stress levels of menopausal women will be assessed using the Perceived Stress Scale (PSS-10). Higher scores indicate higher perceived stress.

Secondary

MeasureTime frameDescription
Menopause AttitudeBaseline and 4 weeks after interventionChanges in attitudes toward menopause will be assessed using the Menopause Attitude Scale. Higher scores reflect more positive attitudes toward menopause.
State MindfulnessBaseline and 4 weeks after interventionChanges in mindfulness levels will be assessed using the State Mindfulness Scale. Higher scores indicate greater mindfulness awareness.

Countries

Turkey (Türkiye)

Contacts

CONTACTCEMRE ÇİLİNGİR, MSc Student
cemrecilingir3103@gmail.com+90 536 274 36 46
STUDY_CHAIRNAZLI BALTACI, Assoc. Prof. Dr.

Ondokuz Mayis University Faculty of Health Sciences

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 30, 2026