Protocol for a partially nested randomised controlled trial to evaluate the effectiveness of the scleroderma patient-centered intervention network COVID-19 home-isolation activities together (SPIN-CHAT) program to reduce anxiety among at-risk scleroderma patients.
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Thombs Brett D, Kwakkenbos Linda, Carrier Marie-Eve, Bourgeault Angelica, Tao Lydia, Harb Sami, Gagarine Maria, Rice Danielle, Bustamante Laura, Ellis Kelsey, Duchek Delaney, Wu Yin, Bhandari Parash Mani, Neupane Dipika, Carboni-Jiménez Andrea, Henry Richard S, Krishnan Ankur, Sun Ying, Levis Brooke, He Chen, Turner Kimberly A, Benedetti Andrea, Culos-Reed Nicole, El-Baalbaki Ghassan, Hebblethwaite Shannon, Bartlett Susan J, Dyas Laura, Patten Scott, Varga John, Scleroderma Patient-centered Intervention Network (SPIN) COVID-19 Patient Advisory Team, SPIN Investigators
Аннотация
METHODS: The SPIN-CHAT Trial is a pragmatic RCT that will be conducted using the SPIN-COVID-19 Cohort, a sub-cohort of the SPIN Cohort. Eligible participants will be SPIN-COVID-19 Cohort participants without a positive COVID-19 test, with at least mild anxiety (PROMIS Anxiety 4a v1.0 T-score ≥ 55), not working from home, and not receiving current counselling or psychotherapy. We will randomly assign 162 participants to intervention groups of 7 to 10 participants each or waitlist control. We will use a partially nested RCT design to reflect dependence between individuals in training groups but not in the waitlist control. The SPIN-CHAT Program includes activity engagement, education on strategies to support mental health, and mutual participant support. Intervention participants will receive the 4-week (3 sessions per week) SPIN-CHAT Program via videoconference. The primary outcome is PROMIS Anxiety 4a score immediately post-intervention.
ETHICS AND DISSEMINATION: The SPIN-CHAT Trial will test whether a brief videoconference-based intervention will improve mental health outcomes among at-risk individuals during contagious disease outbreak.