Clinical trial · Interventional
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
- Retrieved
- Sep 18, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260918-000001
Summary
Brief summary (as posted)
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.
Conditions
Conditions (5)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Adolescent and Young Adult With Brain Cancer | — | UNRESOLVED | — |
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
| Pediatric Cancer | Childhood Malignant Neoplasm | ALIAS | 0.90 |
| Pediatric Malignancies | — | UNRESOLVED | — |
| Pediatric Sarcoma of Soft Tissue | Childhood Soft Tissue Sarcoma | ALIAS | 0.90 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| ARTCan App | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Digital Art Therapy
- description
- All participants will receive art therapy via the ARTCan App for 6 weeks, and will also be prompted to complete mental health quality of life surveys at baseline and each week, which will be available for the therapist to review.
- interventionNames
- Behavioral: ARTCan App
Primary outcomes (1)
- measure
- Feasibility of art therapy
- timeFrame
- Up to 6 weeks
- description
- The feasibility of art therapy will be determined by the proportion of participants who complete art therapy. The proportion of participants who complete 4 of the 6 art therapy modules will be determined. A completion rate of 10 out of 15 participants will be deemed feasible.
Secondary outcomes (1)
- measure
- Acceptability of art therapy
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 25 Years
Show eligibility criteria text
Inclusion Criteria: 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)?". Exclusion Criteria: * 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. * Other conditions or factors which in the opinion of the Pl would not make the patient a good candidate for the study.
References
Publications (0)
Data not yet available