Mobile Self Management and Support for Adolescents and Young Adults With Cancer
Primary Purpose
Sarcoma
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Pocket Coach for AYA with Cancer
Sponsored by
About this trial
This is an interventional supportive care trial for Sarcoma
Eligibility Criteria
Inclusion Criteria:
- Parent or self-reported (for participants 18+ years old) physician diagnosis of sarcoma
- Daily use of a smartphone (iOS, Android, or Windows) or tablet
- Current Facebook account that participant can use to participate in the focus group (or, be willing to create a Facebook account for this purpose).
- Able and willing to give informed assent and comply with study requirements
- For patients aged 13-17 years, have one caregiver willing and able to participate in the study
- Able to read and speak English
Exclusion Criteria:
- Patients that are not able to participate in the study due to their medical condition and/or treatment regimen, as determined by the patients' treating oncologist in conjunction with patients' family members
- Inability to provide informed assent/permission/consent
- Inability to read, speak, and understand English
Sites / Locations
- UCLA Pediatric Pain Program Research Offices
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Mobile application
Arm Description
Outcomes
Primary Outcome Measures
Feasibility
Determined by the number of days participants use the program. Program usage will be assessed on the back end of the technology platform, which tracks how often each participant opens the app and uses any of the features. Intervention will be deemed feasible if participants use the program on at least two thirds of the 30 days in the study period (i.e., 20 out of the 30 days).
Secondary Outcome Measures
Change in level of mindfulness
Assessed by the change in the total score on the Child and Adolescent Mindfulness Measure (CAMM) from pre-intervention to post-intervention. Calculated by subtracting the pre-intervention score from the post-intervention score. The CAMM is a 10-item measure whose total score can range from 0-40. Higher scores correspond to higher levels of mindfulness.
Full Information
NCT ID
NCT03130751
First Posted
April 21, 2017
Last Updated
October 9, 2017
Sponsor
University of California, Los Angeles
Collaborators
BodiMojo, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT03130751
Brief Title
Mobile Self Management and Support for Adolescents and Young Adults With Cancer
Official Title
Mobile Self Management and Support for Adolescents and Young Adults With Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
October 2017
Overall Recruitment Status
Completed
Study Start Date
May 23, 2017 (Actual)
Primary Completion Date
August 10, 2017 (Actual)
Study Completion Date
August 10, 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of California, Los Angeles
Collaborators
BodiMojo, Inc.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
This study is the user testing phase of a mobile application intervention which will be designed to promote positive coping skills, illness resilience, and social support, and to serve as a complement to patient-physician interactions in adolescents and young adults (AYA) with sarcoma. User testing will be conducted with a prototype of the app. Participants will be AYA ages 13-25 with sarcoma (N=16). Study participation involves the AYAs downloading and using the app for 30 days. During the 30 days, participants will interact with the app by inputting their current mood, receiving supportive feedback from the app, reading messages, and doing brief activities (such as relaxation activities, etc.). Participants will also participate in an online focus group focused around the user experience. Before and after the 30 days of user testing, participants will complete a few brief questionnaires about their behavior, how their symptoms affect their life, and how they receive support from others. These questions will take around 20 minutes to complete at each administration.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sarcoma
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Mobile application
Arm Type
Experimental
Intervention Type
Behavioral
Intervention Name(s)
Pocket Coach for AYA with Cancer
Intervention Description
The Pocket Coach for AYA with Cancer is a psychosocial intervention to be delivered through a mobile platform. Intervention content is based on Mindfulness Based Stress Reduction (MBSR) and the Resilience in Illness Model [Dr. Joan E. Haase et al] and includes modules on relaxation, mindfulness, cognitions, and self-compassion.
Primary Outcome Measure Information:
Title
Feasibility
Description
Determined by the number of days participants use the program. Program usage will be assessed on the back end of the technology platform, which tracks how often each participant opens the app and uses any of the features. Intervention will be deemed feasible if participants use the program on at least two thirds of the 30 days in the study period (i.e., 20 out of the 30 days).
Time Frame
30 days (from day 1 through day 30 of the 30-day intervention period)
Secondary Outcome Measure Information:
Title
Change in level of mindfulness
Description
Assessed by the change in the total score on the Child and Adolescent Mindfulness Measure (CAMM) from pre-intervention to post-intervention. Calculated by subtracting the pre-intervention score from the post-intervention score. The CAMM is a 10-item measure whose total score can range from 0-40. Higher scores correspond to higher levels of mindfulness.
Time Frame
Pre-intervention to post-intervention (a span of 30 days)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
13 Years
Maximum Age & Unit of Time
25 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Parent or self-reported (for participants 18+ years old) physician diagnosis of sarcoma
Daily use of a smartphone (iOS, Android, or Windows) or tablet
Current Facebook account that participant can use to participate in the focus group (or, be willing to create a Facebook account for this purpose).
Able and willing to give informed assent and comply with study requirements
For patients aged 13-17 years, have one caregiver willing and able to participate in the study
Able to read and speak English
Exclusion Criteria:
Patients that are not able to participate in the study due to their medical condition and/or treatment regimen, as determined by the patients' treating oncologist in conjunction with patients' family members
Inability to provide informed assent/permission/consent
Inability to read, speak, and understand English
Facility Information:
Facility Name
UCLA Pediatric Pain Program Research Offices
City
Los Angeles
State/Province
California
ZIP/Postal Code
90064
Country
United States
12. IPD Sharing Statement
Citations:
PubMed Identifier
33844938
Citation
Donovan E, Martin SR, Seidman LC, Zeltzer LK, Cousineau TM, Payne LA, Knoll M, Weiman M, Federman NC. The Role of Social Media in Providing Support from Friends for Adolescent and Young Adult (AYA) Patients and Survivors of Sarcoma: Perspectives of AYA, Parents, and Providers. J Adolesc Young Adult Oncol. 2021 Dec;10(6):720-725. doi: 10.1089/jayao.2020.0200. Epub 2021 Apr 12.
Results Reference
derived
PubMed Identifier
30882352
Citation
Donovan E, Martin SR, Seidman LC, Zeltzer LK, Cousineau TM, Payne LA, Trant M, Weiman M, Knoll M, Federman NC. A Mobile-Based Mindfulness and Social Support Program for Adolescents and Young Adults With Sarcoma: Development and Pilot Testing. JMIR Mhealth Uhealth. 2019 Mar 18;7(3):e10921. doi: 10.2196/10921.
Results Reference
derived
Learn more about this trial
Mobile Self Management and Support for Adolescents and Young Adults With Cancer
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