Bridging the Gap: Using Video Art to Document the Human Face of Disease & Predict Quality of Life Assessments in Brain Tumor Patients

Sponsor
Indiana University (Other)
Overall Status
Unknown status
CT.gov ID
NCT02890940
Collaborator
(none)
50
1
45

Study Details

Study Description

Brief Summary

The goal of this study is to explore whether facial expression changes in visual portraits correlate with Quality of Life (QOL) questionnaire responses before and after pet therapy sessions and to compare scores of QOL questionnaires before and after pet therapy.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Pet Therapy
N/A

Detailed Description

Through this pilot study, the investigators propose to create new intersections between video art and clinical care by photographing and videotaping patients with brain tumors before, during and after pet therapy sessions. This exploratory scholarship has two equally compelling goals. First, the artistic component of the project aims to create compelling slow motion video portraits of patients' willing to share their experiences of what it is like to confront such a grave illness. The goal is to put a human face on disease and share the endurance of the human spirit through art. Second, the scientific component will assess the potential of using facial video portraits as a novel and innovative way to measure Quality of Life (QOL) in lieu of questionnaires in brain tumor patients. In addition, the project will evaluate the effects of pet therapy on the QOL of these patients.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Primary Purpose:
Supportive Care
Official Title:
Bridging the Gap: Using Video Art to Document the Human Face of Disease & Predict Quality of Life Assessments in Brain Tumor Patients
Study Start Date :
Aug 1, 2016
Anticipated Primary Completion Date :
May 1, 2020
Anticipated Study Completion Date :
May 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Pet Therapy

Behavioral: Pet Therapy
Patients will be asked to complete the standardized QLQ-C30/BN20 questionnaires. Following completion of the questionnaires, a trained pet therapy dog will be brought to the patients for approximately 10 minutes. After approximately 10 minutes, the dog will be removed and the patients will be asked to re-complete the standardized QLQ-C30/BN20 questionnaires. Patients will be photographed and videographed during this time. Finally, patients will be asked to talk about how their perspectives on life have changed with their diagnosis. These responses will be captured for use in the art exhibit created from images collected during the study.

Outcome Measures

Primary Outcome Measures

  1. Correlation of facial expression changes with QOL questionnaire responses [Immediately prior to therapy session to immediately after therapy session]

    Will look to see if there is a correlation between facial expression changes in visual portraits with QOL questionnaire responses before and after pet therapy sessions

Secondary Outcome Measures

  1. Comparison of scores of QOL questionnaires before and after pet therapy [Immediately prior to therapy session to immediately after therapy session]

    Will compare QOL questionnaire scores from before and after pet therapy sessions to see if there is a change after the pet therapy.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with brain tumors

  • Willingness to participate in a brief pet therapy session with a dog

  • Willingness to allow photographs, pictures and audio used in an art exhibit

Exclusion Criteria:
  • Allergy to dogs

  • Concurrent disease or condition that would make the patient inappropriate for study participation or any serious medical or psychiatric disorder that would interfere with the subject's safety

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Indiana University

Investigators

  • Principal Investigator: Mahua Dey, MD, Indiana University
  • Principal Investigator: Stefan Petranek, Indiana University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Mahua Dey, Neurosurgeon, Indiana University
ClinicalTrials.gov Identifier:
NCT02890940
Other Study ID Numbers:
  • 1604467360
First Posted:
Sep 7, 2016
Last Update Posted:
Oct 9, 2018
Last Verified:
Oct 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 9, 2018