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Electronic patient-reported outcome measure and decision support tool option for early intervention service quality: a pilot cluster-randomized pragmatic trial
Children’s Participation in Environment Research Lab, University of Illinois Chicago, IL, USA;Department of Occupational Therapy, University of Illinois Chicago, IL USA;Department of Computer Science, University of Illinois Chicago, IL USA.
Children’s Participation in Environment Research Lab, University of Illinois Chicago, IL, USA;Department of Occupational Therapy, University of Illinois Chicago, IL USA.ORCID iD: 0000-0002-9895-0922
Center for Clinical and Translational Science, University of Illinois Chicago, IL, USA.ORCID iD: 0000-0002-6802-9243
Rocky Mountain Human Services, Denver, CO, USA.
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2026 (English)In: Advances in Rehabilitation Science and Practice, ISSN 2753-6351, Vol. 15, p. 1-14Article in journal (Refereed) Published
Abstract [en]

Introduction:The Young Children’s Participation in Environment Measure (YC-PEM) is an evidence-based and promising electronic patient-reported outcome (e-PRO) option to improve early intervention (EI) service quality, such as when designing the EI service pla.

Aim:Establish the preliminary effectiveness of implementing the YC-PEM e-PRO and program-specific shared decision support tool option for EI service quality when designing a service plan.

Methods:For this 2-arm pilot pragmatic trial with cluster randomization at the provider level, 76 caregivers enrolled and 57 caregivers (n = 29 intervention group; n = 28 control group) completed pre- and post-intervention measures. Intervention group caregivers completed the YC-PEM e-PRO and program-specific shared decision support tool and were compared to usual care on EI service quality indicators: (1) caregiver perceptions of family-centeredness, (2) caregiver activation for shared decision-making, (3) caregiver engagement in service design and implementation; and (4) service plan quality.

Results:No significant group differences at baseline were noted. Pre-post EI service quality revealed no significant differences in the adjusted model (P > .05). However, intervention group families had higher rates participation-focused service plans (69.2%) versus controls (51.4%), most of which met state-level criteria for quality (84%).

Conclusion:For EI service quality indicators, this intervention option demonstrated comparable performance to usual care. This finding suggests the intervention promoted high quality, participation-focused service planning despite no overall differences in EI service quality, warranting further testing of implementation factors and effectiveness in various service contexts.

Trial Registration Number: NCT04562038

Place, publisher, year, edition, pages
Sage Publications, 2026. Vol. 15, p. 1-14
Keywords [en]
rehabilitation, rehabilitation process, clinical decision support, early intervention, social, participation
National Category
Health Care Service and Management, Health Policy and Services and Health Economy
Identifiers
URN: urn:nbn:se:umu:diva-256940DOI: 10.1177/27536351261445239ISI: 001759095200001OAI: oai:DiVA.org:umu-256940DiVA, id: diva2:2088825
Funder
NIH (National Institutes of Health), UL1TR002003NIH (National Institutes of Health), UL1TR002003Available from: 2026-07-30 Created: 2026-07-30 Last updated: 2026-07-30Bibliographically approved

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Kaelin, Vera C.Rizk, SabrinChen, Yi-FanLeland, Natalie E.Murphy, Natalie J.Lage, Carla R.Villegas, VivianKhetani, Mary A.
Health Care Service and Management, Health Policy and Services and Health Economy

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CiteExportLink to record
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