Maintaining Engagement in Adults with Neurofibromatosis Type 1 to Use the iCanCope Mobile Application (iCanCope-NF)

Author:

Buono Frank D.1ORCID,Larkin Kaitlyn1,Pham Quynh23,De Sousa Diane2,Zempsky William T.45,Lalloo Chitra36,Stinson Jennifer N.67ORCID

Affiliation:

1. Department of Psychiatry, Yale School of Medicine, New Haven, CT 06510, USA

2. Centre for Digital Therapeutics, University Health Network, Toronto, ON M5G 2C4, Canada

3. Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON M5T 3M6, Canada

4. Department of Pain and Palliative Medicine, Connecticut Children’s Medical Center, Hartford, CT 06106, USA

5. Department of Pediatrics and Nursing, University of Connecticut School of Medicine, Stores, CT 06032, USA

6. The Research Institute, The Hospital of Sick Children, Toronto, ON M5G 1X8, Canada

7. Lawrence S. Bloomberg Faculty of Nursing, University of Toronto, Toronto, ON M5T 1P8, Canada

Abstract

Introduction: Neurofibromatosis Type 1 (NF1) is an autosomal dominant genetic condition in which chronic pain is a predominant issue. Given the rarity of the disease, there are limited psychosocial treatments for individuals with NF1 suffering with chronic pain. Using mobile applications can facilitate psychosocial treatments; however, there are consistent issues with engagement. Utilizing a mixed methodology, the current study evaluated the customized iCanCope mobile application for NF1 on increasing engagement through the usage of contingency management. Methods: A mixed methods study from a subset of data coming from a randomized clinical trial that occurred from January 2021 to August 2022 was undertaken. Two groups (iCC and iCC + CM) were exposed to the customized iCanCope mobile application in which engagement data were captured in real-time with daily check-ins for interference, sleep, mood, physical activity, energy levels, goal setting, and accessing article content (coping strategies). Additionally, semi-structured interviews were conducted to gain insight into the participants’ experience at the end of the trial. Results: Adults (N = 72) were recruited via NF patient advocacy groups. Significant differences were noted between the groups in total articles read (p = 0.002), goals achieved (p = 0.017), and goals created (p = 008). Additionally, there were significant differences observed between user-generated goals and those that were app recommended (p < 0.001). Both groups qualitatively reported positive feedback on the customized mobile application, indicating that continued usage and engagement of the mobile application were acceptable. Conclusions: Employing customized mobile applications for adults with NF1 along with contingency management can leverage self-managed pain treatments while providing auxiliary resources to this population.

Funder

the U.S. Army Medical Research Materiel Command

Publisher

MDPI AG

Subject

Cancer Research,Oncology

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