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Co-Designed Digital Device for Tracking Rehabilitation Dosage in a Clinical Environment After Stroke: Mixed Methods Validity and Feasibility Study

Co-Designed Digital Device for Tracking Rehabilitation Dosage in a Clinical Environment After Stroke: Mixed Methods Validity and Feasibility Study

This study received ethical approval from the Strathclyde University Ethics Committee under the protocol number UEC20/08: Kerr: Generic Framework Application: User experience of a technology-based rehabilitation program. All participants provided informed consent before their involvement in the study. Participants did not receive compensation, and all data were anonymized.

Fiona Boyd, Gillian Sweeney, Mark Barber, Elaine Forrest, Mark Dunlop, Andrew Kerr

JMIR Rehabil Assist Technol 2025;12:e68129