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Utilizing the Arts to Improve Health, Resilience, and Well-Being Among Cancer Patients and Their Caregivers

Utilizing the Arts to Improve Health, Resilience, and Well-Being in Individuals With Cancer and Their Caregivers: A Feasibility Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03272880
Enrollment
6
Registered
2017-09-06
Start date
2017-09-25
Completion date
2018-04-13
Last updated
2018-04-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cancer

Keywords

Art Therapy, Music Therapy

Brief summary

The purpose of this study is to evaluate the impact of arts-based programming on health, well-being, and resilience. Patients who have cancer or are the caregivers of someone with cancer are being asked to take part in this study.

Detailed description

Objective: Primary: To assess the feasibility and acceptability of arts-based programming for community-dwelling cancer survivors and caregivers. Feasibility and acceptability will be assessed based on: 1. Recruitment 2. Participation 3. Retention (drop-outs) 4. Satisfaction Secondary: To assess the participants' ability to: 1. Define goals and strategies using the contents of the program. 2. Implement the strategies in their daily activities in the short-term. 3. Continue to use these strategies after the program ends. Exploratory: To perform exploratory analyses on the impact of arts-based programming on health, resilience, and well-being.

Interventions

BEHAVIORALArts-Based Programming

This feasibility study includes educational components and an experiential components which are assessed with pre- and post-tests. The topics of these components include: Introduction to the Arts and Health; Music, Well-Being, and Resilience; Movement and Physical Activity; Art and Well-Being; Theater and Socialization; Art Appreciation and a Healthy Brain; and Summary/Integration of the Arts into Daily Lives. The impact of this program will be assessed with qualitative follow-up interviews.

Sponsors

Case Comprehensive Cancer Center
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

This will be a pre-post intervention observational study utilizing a mixed methods approach

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Able to participate in all program sessions * Cognitively able to consent to participate * Speaks, reads, and writes English * Diagnosis of cancer or caregiver of someone with cancer

Exclusion criteria

* Severe visual or auditory impairment * Severe and/or uncontrolled comorbidity precluding safe participation in a physical activity program

Design outcomes

Primary

MeasureTime frameDescription
Feasibility: Number of participants recruited in the studyUp to 8 weeks after beginning of studyStudy will be feasible if recruitment goal is met with 10-20 participants enrolled
Feasibility: Average number of session attended by participantsUp to 8 weeks after beginning of studyStudy will be feasible if average number of session attended will be greater than or equal to 4
Percent of patients who drop out of studyUp to 8 weeks after beginning of studyStudy will be feasible if no more than 25% of patients drop out of study
Satisfaction ScoreUp to 8 weeks after beginning of studySatisfaction will be high in post-test surveys

Secondary

MeasureTime frameDescription
Qualitative Impact of arts based programming on resilienceUp to 3 weeks after final session (11 weeks from beginning of study)Impact of program on resilience described in phenomenological interviews
Qualitative Impact of arts based programming on well-beingUp to 3 weeks after final session (11 weeks from beginning of study)Impact of program on well-being described in phenomenological interviews
Qualitative Impact of arts-based programming on healthUp to 3 weeks after final session (11 weeks from beginning of study)Impact of program on health described in phenomenological interviews

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026