Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07464626

Virtual vs Physical Art Therapy for Anxiety, Psychological Well-being, and Sleep Quality in Colorectal Cancer Patients

Led by Dokuz Eylul University · Updated on 2026-03-11

78

Participants Needed

1

Research Sites

95 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This randomized controlled trial aims to evaluate the effects of virtual reality-based art therapy and physical art therapy on anxiety, psychological well-being, and sleep quality in patients with colorectal cancer receiving outpatient chemotherapy. A total of 78 patients will be randomly assigned to three groups: a virtual reality art therapy group, a physical art therapy group, and a control group. Participants in the intervention groups will receive art therapy sessions every two weeks for eight weeks (four sessions in total). Anxiety, psychological well-being, and sleep quality will be assessed using validated scales before the intervention and after the fourth session. The findings are expected to contribute to the development of non-pharmacological supportive care interventions for oncology patients.

CONDITIONS

Official Title

Virtual vs Physical Art Therapy for Anxiety, Psychological Well-being, and Sleep Quality in Colorectal Cancer Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 18 years or older
  • Diagnosed with colorectal cancer
  • Receiving outpatient chemotherapy (FOLFOX or XELOX regimen)
  • ECOG performance status between 0 and 2
  • Not receiving radiotherapy
  • No hearing or speech impairments
  • No severe psychiatric disorders (e.g., schizophrenia, major depression, bipolar disorder)
  • Able to understand the study procedures and provide informed consent
  • Willing to participate in the study
Not Eligible

You will not qualify if you...

  • ECOG performance status of 3 or higher
  • Patients who do not meet the inclusion criteria
  • Patients unwilling to participate in the study

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Dokuz Eylul University Hospital

Izmir, Balçova, Turkey (Türkiye), 35330

Actively Recruiting

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Research Team

E

Esra Uslu Tanis, Msc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

3

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