NCT06127121
Recruiting
Not Applicable
A Digital Art Activity to Enhance Self-Disclosure and the Detection of Psycho-social Distress in Adult Cancer Patients
M.D. Anderson Cancer Center1 site in 1 country60 target enrollmentStarted: November 2, 2023Last updated:
ConditionsCancer
Overview
- Phase
- Not Applicable
- Status
- Recruiting
- Sponsor
- M.D. Anderson Cancer Center
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- The Edmonton Symptom Assessment System, (ESAS) questionnaires
Overview
Brief Summary
To look at how a digital art activity may help cancer patients improve their ability to express their distress, symptoms, and lived experience.
Detailed Description
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.
Study Design
- Study Type
- Observational
- Observational Model
- Cohort
- Time Perspective
- Prospective
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
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
Outcomes
Primary Outcomes
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
Secondary Outcomes
No secondary outcomes reported
Investigators
Study Sites (1)
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