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Completed

NCT Number: NCT07435597

Comparing the Effects of Art Therapy and Mandala Application on State Anxiety Levels in Chemotherapy Patients

The research is planned as a randomized controlled trial with a two-group (art-based flow drawing and mandala), pre-test, post-test design.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Basaksehir Cam Sakura Hospital

Istanbul, 34000, Turkey (Türkiye)

About this study

This study aims to compare the effects of the "Dance of the Pen" (art-based flow drawing) and mandala activities on state anxiety in patients undergoing chemotherapy and to evaluate intervention satisfaction. The research is planned as a randomized controlled trial with a two-group, pre-test, post-test design. The study will be conducted in two hospitals in Istanbul with a total of 60 participants. The intervention group will receive the "Dance of the Pen" and mandala activities. Randomization will be based on the patients' chemotherapy session days, and the study will be conducted as a single-blind study. Data will be collected using a Personal Information Form, the State Anxiety Scale (STAI-I), and a Distress Thermometer. Interventions will be applied in structured sessions lasting approximately 30-60 minutes. The population of the study will consist of patients receiving chemotherapy at hospital, and those patients meeting the inclusion criteria will constitute the sample of the study. Participants will be informed about the study before the research begins. Those who agree to participate will be assigned to a randomized group and will undergo either the "Dance of the Pen" or "Mandala activity," both conducted as single-session interviews. Participants will complete a Personal Information Form and the STAI-I before the activity, and will also undergo the STAI-I and distress thermometer tests afterwards.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Must be 18 years of age or older
  • Must be receiving chemotherapy treatment
  • Must be willing to participate in the research
  • Must be literate
  • Must be able to speak and understand Turkish

Exclusion criteria

  • -Having any speech or comprehension impairment
  • Being treated with other forms of treatment
  • Having any accompanying psychiatric diagnosis
  • Using any psychiatric medication
  • Being enrolled in another program using a similar method could affect the study's outcome

Treatment and study plan

Mandala therapy

Other

Patients will be given a file containing mandala designs, and they will be asked to color the design of their choice with their preferred colored pencils (pastel, crayon, marker) throughout the treatment.

Art therapy

Other

During chemotherapy, the patient will be given a pen to hold with their eyes closed and asked to draw on a blank piece of paper according to the instructions. Afterwards, their drawing will be analyzed and interpreted.

Primary outcomes

  1. State anxiety scale

    Time frame: 6 months

    The State Anxiety Scale will be administered prior to the intervention, followed by randomly assigned art therapy or mandala practice. The State Anxiety Scale and distress thermometer will be administered again after the intervention is completed. A high score on the State Anxiety Scale indicates high anxiety levels.

Sponsors and collaborators

Lead sponsor

Atlas University

Other

Registry information

Official study title

Comparing the Effects of Art Therapy and Mandala Application on State Anxiety Levels in Chemotherapy Patients: A Randomized Controlled Study

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Feb 27, 2026
Registry last updated
Jun 18, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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