PT - JOURNAL ARTICLE AU - Lessard, David AU - Engler, Kim AU - Yuanchao, MA AU - Baradaran, Ashkan AU - Cox, Joseph AU - Hijal, Tarek AU - Costiniuk, Cecilia AU - de Pokomandy, Alexandra AU - Lebouché, Bertrand TI - Feasibility and Acceptability of Using an Electronic Patient-Reported Outcome Measure via a Patient Portal in HIV care AID - 10.1370/afm.22.s1.6158 DP - 2024 Nov 20 TA - The Annals of Family Medicine PG - 6158 VI - 22 IP - Supplement 1 4099 - http://www.annfammed.org/content/22/Supplement_1/6158.short 4100 - http://www.annfammed.org/content/22/Supplement_1/6158.full SO - Ann Fam Med2024 Nov 20; 22 AB - Context: Adherence to antiretrovirals (ART) is essential for people with HIV (PWH), but many face barriers. The I-Score is a new electronic patient-reported outcome measure (ePROM) of ART adherence barriers to be used in HIV care.Objective: To assess the feasibility and acceptability of administering the I-Score on a patient portal.Study Design Analysis: 6-month one-arm implementation pilot study.Setting: A large hospital-based clinic in Montreal, Canada.Population: PWH on ART, speaking French or English, owning a smartphone, willing to use the patient portal, reporting adherence issues.Intervention/Instrument: Patients visited their HIV physician at Time 1 (T1), 3 months (T2), and 6 months (T3). Before visits, they completed the I-Score. After visits, they completed a survey on sociodemographic characteristics (T1), and feasibility and acceptability of the I-Score.Outcome Measures: Feasibility was assessed with consent and retention rates; frequency of technological problems; and the 4-item Feasibility of Intervention Measure (FIM). Acceptability was evaluated with the adapted 6-item Acceptability E-scale for web-based PROMs (AES); and the 4-item Acceptability of Intervention Measure (AIM). We provide descriptive statistics.Results: Out of 34 PWH with identified adherence issues, 32/34 (94%) consented. Average age was 48 years (standard deviation (SD)=15), 12/32 (38%) were women, 19/32 (59%), migrants, and 10/32 (31%) lived below the poverty line. Overall, 26/32 (81%) completed the study, for a total of 78 visits; 4 were lost-to-follow-up and 2 withdrew due to difficulties with technology. During T1, T2, and T3, there were 12/26 (46%), 17/26 (65%), and 16/26 (62%) participants, respectively, reporting no technological problem. Problems met included needing to: remind patients to complete the I-Score before medical visit (15 visits); re-initialize passwords (8); resolve connectivity issues (2); and re-install the patient portal (2). Physicians could not access I-Score results at 4 visits; 10 visits were postponed due to difficulties. Average scores on FIM increased from 17/20 (T1;SD=5), to 18/20 (T2;2), to 19/20 (T3;2). Average AES increased from 24/30 (SD=5), to 26/30 (3), to 27/30 (3). Average AIM scores passed from 16/20 (5), to 18/20 (2), to 17/20 (3).Conclusions: The feasibility and acceptability of using a patient portal to administer the I-Score ePROM was high for vulnerable PWH, but use was challenged by patient literacy and technology.