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

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Turkey
Artvin State Hospital
RECRUITING
Artvin
Contact Information
Primary
Efe Hasdemir Efe Hasdemir, MD
hasdemir52@gmail.com
+90 5433750709
Time Frame
Start Date: 2026-01-27
Estimated Completion Date: 2027-01-20
Participants
Target number of participants: 60
Treatments
Experimental: Mandala Coloring Group
Participants will perform mandala coloring for 30 minutes during outpatient chemotherapy in addition to routine care.
No_intervention: Control group
Participants will receive routine outpatient chemotherapy care without any additional activity.
Related Therapeutic Areas
Sponsors
Leads: Artvin Coruh University

This content was sourced from clinicaltrials.gov