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Recruiting NCT07367269

NCT07367269 Effect of Mandala Coloring on Anxiety, Distress, and Comfort in Breast Cancer Patients Receiving Outpatient Chemotherapy

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Clinical Trial Summary
NCT ID NCT07367269
Status Recruiting
Phase
Sponsor Artvin Coruh University
Condition Breast Cancer
Study Type INTERVENTIONAL
Enrollment 60 participants
Start Date 2026-01-27
Primary Completion 2027-01-20

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Mandala Coloring

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 60 participants in total. It began in 2026-01-27 with a primary completion date of 2027-01-20.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Breast cancer patients receiving chemotherapy often experience psychological distress, anxiety, and discomfort during treatment. Non-drug supportive methods may help improve patients' well-being during chemotherapy. This study aims to evaluate whether mandala coloring during outpatient chemotherapy can reduce psychological distress and anxiety and improve comfort in breast cancer patients. Participants will be randomly assigned to either a mandala coloring group or a routine care group. Patients in the intervention group will color mandala patterns for 30 minutes during their chemotherapy session, while the control group will receive routine care only. Psychological distress, anxiety, and comfort levels will be measured before and after the chemotherapy session in both groups. The results of this study may provide evidence for a simple and low-cost supportive intervention to improve the psychological well-being of breast cancer patients during chemotherapy.

Eligibility Criteria

Inclusion Criteria: * Being 18 years of age or older * Having a diagnosis of breast cancer and receiving chemotherapy * Having no communication problems * Having no physical disability that would prevent mandala coloring * Being willing to participate in the study Exclusion Criteria: * not meeting inclusion criteria

Contact & Investigator

Central Contact

Efe Hasdemir Efe Hasdemir, MD

✉ hasdemir52@gmail.com

📞 +90 5433750709

Frequently Asked Questions

Who can join the NCT07367269 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Breast Cancer. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07367269 currently recruiting?

Yes, NCT07367269 is actively recruiting participants. Contact the research team at hasdemir52@gmail.com for enrollment information.

Where is the NCT07367269 trial being conducted?

This trial is being conducted at Artvin, Turkey (Türkiye).

Who is sponsoring the NCT07367269 clinical trial?

NCT07367269 is sponsored by Artvin Coruh University. The trial plans to enroll 60 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology