Skip to main content
OpenTrials
Recruiting

NCT Number: NCT06127121

A Digital Art Activity to Enhance Self-Disclosure and the Detection of Psycho-social Distress in Adult Cancer Patients

To look at how a digital art activity may help cancer patients improve their ability to express their distress, symptoms, and lived experience.

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

MD Anderson Cancer Center

Houston, Texas, 77030, United States

Location status: Recruiting

Location contact

Carlos Roldan, MD

CONTACT

[email protected]

713-563-7402

Carlos Roldan, MD

PRINCIPAL_INVESTIGATOR

About this study

Primary objective:

  • To evaluate how engaging in a digital art activity might potentially cause changes in symptom reporting, based on pre/post self-reporting on the Edmonton Symptom Assessment System (ESAS) at time T3.

Secondary objectives:

  • To evaluate the changes in symptom reporting, based on pre/post self-reporting on ESAS at different times of the study (T1, T2).
  • To evaluate how a specific creative art making activity (T3), compared to an active control condition (T2; music listening) may or may not impact reporting ESAS.
  • To monitor potential changes in distress disclosure, based on the self-report scoring on the Distress Disclosure Index score at T0, T2 and T3.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age equal or greater than 18 years
  • Patients who are admitted in the hospital and have received a cancer diagnosis.
  • Suffering from solid cancer or hematological malignancy and receiving active treatment for their cancer.
  • Voluntary written consent.
  • Fluent in English or Spanish.

Exclusion criteria

  • Not being able to use a digital tablet
  • Being speech impaired or vision impaired
  • Patients who are cognitively impaired and unable to read or consent for the study
  • Pregnant women

Treatment and study plan

Digital Art Activity

Behavioral
  • complete a symptom questionnaire
  • complete another activity such as listening to meditative music for 10 minutes
  • fill out the symptom questionnaire and engage in the digital art activity again

Primary outcomes

  1. The Edmonton Symptom Assessment System, (ESAS) questionnaires

    Time frame: through study completion; an average 1 year.

    Score Scale (0-10) 0 No symptom-10 Worst possible

Study contacts

Contact information is provided by the study sponsor or research team.

Carlos Roldan, MD

CONTACT

[email protected]

(713) 563-7402

Sponsors and collaborators

Lead sponsor

M.D. Anderson Cancer Center

Other

Registry information

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Nov 13, 2023
Registry last updated
May 20, 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.

Published trials that share one or more normalized conditions with this study.