NCT06789666Terminated
Digital Art Therapy for Young Cancer Survivors
Feasibility of a Digital Art Therapy Application Designed to Improve Quality of Life in Young Cancer Survivors
Source: ClinicalTrials.gov · Last updated 15 Oct 2026
Brief summary (registry, in English)
This is a single-site, single-arm, interventional study assessing the feasibility of the ARTCan Therapy Application (App) and whether it is an acceptable means of administering art therapy to young adult cancer survivors. The ARTCan Therapy App guides participants through a 6-week digital art therapy program. Subjects will participate in weekly art therapy prompts guided by the app and will complete weekly mental health quality of life (MHQoL) surveys during the intervention. In addition, baseline and end-of-intervention patient-reported outcome measures (PROMIS-DSF8a) and an acceptability survey will be administered. The hypothesis is that digital art therapy is feasible for young adult cancer survivors with self-reported mood issues and is an acceptable means of administering art therapy in the patient population.
- Status (registry)
- Terminated
- Study type
- Interventional
- Enrollment
- 2 (actual)
- First submitted
- 17 Jan 2025
- Start date
- 7 Apr 2025
- Primary completion date
- 28 Aug 2026
- Lead sponsor
- UNC Lineberger Comprehensive Cancer Center
- Diseases
- Sarcoma
- NCT number
- NCT06789666
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Other conditions or factors which in the opinion of the Pl would not make the patient a good candidate for the study.
Other
- All subjects meeting any of the exclusion criteria at baseline will be excluded from study participation.
- Patients who lack interest in art. Screening question: Are you open to making art on a scale from 1-5 (1 being not at all, and 5 being very much; must score 3 or higher).
- Subjects who lack basic technology skills (Screening question: On a scale of 1-5 (1 being uncomfortable, and 5 being very comfortable), how would you rate your comfort using websites. Must score 3 or higher).
- Subjects unable to provide consent.
Who the study is looking for
- In order to participate in this study a subject must meet all of the eligibility criteria outlined below.
- Written informed assent and parental consent obtained to participate in the study and HIPAA authorization for release of personal health information.
- Subject is willing and able to comply with study procedures based on the judgment of the investigator.
- Age 18-25 years at the time of consent.
- Childhood cancer survivor, defined as having cancer between birth 17 years of age and who has completed cancer treatment.
- Reliable internet connection and access to a computer, smartphone, or iPad to support application and virtual study visits.
- Answers "yes" to the question "Do you experience mood issues (yes or no)?".
Age in the registry: 18 years to 25 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Lineberger Comprehensive Cancer Center Coordinator of this site? Confirm its status | Chapel Hill | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.