- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03067766
Comic Art Creation as Supportive Care in Cancer Patients and Caregivers
A Pilot Study to Test the Feasibility of Comic Art Creation for Symptom Management in Cancer Supportive Care
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
PRIMARY OBJECTIVES:
I. To determine the feasibility of using a 10 week (Workshop A) or a 5 week (Workshops B-C) comic art creation workshops for supportive care.
II. To determine the feasibility of studying comic art creation workshops for supportive care.
III. To describe those factors affecting the ability or inability of participants to engage in the workshop.
SECONDARY OBJECTIVES:
I. To describe changes in emotional wellbeing and communication of patients and caretakers/family/friends.
TERTIARY OBJECTIVES:
I. Identify the methods that most engage supportive care patients and caretakers.
II. Identify the social and cultural interactions most impacted by comics creation.
III. To describe participant feedback regarding the intervention and study design.
OUTLINE: Patients are assigned to 1 of 2 arms.
WORKSHOP A: Patients and a family member, caretaker, or friend participate in an artist-led comic art therapy workshop over 2 hours once a week for 10 weeks. Patients and participants receive a range of assignments that focus on creative art and experimentation with materials and storytelling in order to make a series of small handmade books that relate directly or indirectly to their experience with cancer. Patients undergo a qualitative interview over approximately 45 minutes and complete validated questionnaires within 4 weeks prior to the workshop and midway through the workshop.
WORKSHOPS B AND C: Patients participate in an artist-led comic art therapy workshop over 3 hours once a week for 5 weeks. Patients receive a range of assignments that focus on creative art and experimentation with materials and storytelling in order to make a series of small handmade books that relate directly or indirectly to their experience with cancer. Patients undergo a qualitative interview over approximately 45 minutes and complete validated questionnaires within 4 weeks prior to the workshop.
After completion of the study, patients are followed up at 1 and 6 weeks.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
Duarte, California, United States, 91010
- City of Hope Medical Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Documented written informed consent of the participant
Workshop A (2017 - 10 weeks- City of Hope)
- Either one of the following:
- City of Hope (COH) cancer patient (all types and at any time point of their disease) OR
- Caretaker/friend family member of the cancer patient
Workshops B and C (2018 - 5 weeks - City of Hope)
- Cancer patients (all types and at any time point in their disease)
- Note: documentation to confirm this eligibility criteria will not be requested; self-reporting as a cancer patient will be considered adequate
- Ability read and speak English
- Willingness and ability to complete the entire workshop, including the interviews and questionnaires (there is no predetermined qualification with regard to the ability to hold an artist tool; accommodations and creative solutions will be made to facilitate participation)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Workshop A (10 weeks - comic art creation workshop)
Patients and a family member, caretaker, or friend participate in an artist-led comic art therapy workshop over 2 hours once a week for 10 weeks.
Patients and participants receive a range of assignments that focus on creative art and experimentation with materials and storytelling in order to make a series of small handmade books that relate directly or indirectly to their experience with cancer.
Patients undergo a qualitative interview over approximately 45 minutes and complete validated questionnaires within 4 weeks prior to the workshop and midway through the workshop.
|
Ancillary studies
Ancillary studies
Other Names:
Participate in a comic art creation workshop
Undergo qualitative interviews
|
|
Experimental: Workshop B and C (5 weeks - comic art creation workshop)
Patients participate in an artist-led comic art therapy workshop over 3 hours once a week for 5 weeks.
Patients receive a range of assignments that focus on creative art and experimentation with materials and storytelling in order to make a series of small handmade books that relate directly or indirectly to their experience with cancer.
Patients undergo a qualitative interview over approximately 45 minutes and complete validated questionnaires within 4 weeks prior to the workshop.
|
Ancillary studies
Ancillary studies
Other Names:
Participate in a comic art creation workshop
Undergo qualitative interviews
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feasibility of the comic art creation workshop defined as participant completion and psychosocial value of the comic art
Time Frame: Up to 1.5 years
|
The project will be considered feasible if most of the participants complete the study and consider the comic art to have personal meaning, and if an initial power calculation indicates that a sufficiently powered randomized controlled trial is possible given the resources of the study team.
It is anticipated that the psychosocial value of the art will be largely derived from the internal creation process and further assessment of the artistic products will not be conducted.
|
Up to 1.5 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in anxiety and depression as measured by the Hospital Anxiety and Depression Scale questionnaire
Time Frame: Baseline to up to 6 weeks post-workshop
|
Statistical analysis will include Wilcoxon signed ranks test of pre, mid and post workshop HRQOL and symptom assessments.
The Friedman test will be used to measure magnitude of difference within a case.
|
Baseline to up to 6 weeks post-workshop
|
|
Change in health-related quality of life (HRQOL) as measured by the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30
Time Frame: Baseline to up to 6 weeks post-workshop
|
Statistical analysis will include Wilcoxon signed ranks test of pre, mid and post workshop HRQOL and symptom assessments.
The Friedman test will be used to measure magnitude of difference within a case.
|
Baseline to up to 6 weeks post-workshop
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Jaroslava Salman, MD, City of Hope Medical Center
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 16251 (Other Identifier: City of Hope Medical Center)
- NCI-2017-00287 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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