Early Functional Response as a Predictor of Clinical Outcomes in Hand Rehabilitation: A Prospective Feasibility Study Using a Digital Monitoring System

Official title

Early Functional Response as a Predictor of Clinical Outcomes in Hand Rehabilitation: A Prospective Feasibility Study Using a Clinician-Developed Digital Monitoring System

Overview

This study investigates whether early changes observed during the first weeks of hand and upper extremity rehabilitation can predict patient outcomes months later. In rehabilitation practice, clinicians make numerous decisions each session regarding exercise type, frequency, duration, and treatment approach. Most of these decisions are currently made without systematic longitudinal data. This study addresses three fundamental questions using data collected during routine clinical care: (1) Can the rate of improvement in the first weeks of treatment predict functional status months later, across both session-based and milestone-based time points? (2) Are there meaningfully different recovery profiles among hand rehabilitation patients? (3) Is there measurable variation in clinical decision-making among patients with similar profiles, and does this variation relate to outcomes? A digital patient monitoring platform developed by the principal investigator, a physiotherapist and academic researcher specializing in hand rehabilitation serves as the data collection infrastructure. The platform records standard clinical assessment measures in a structured format and has been in active clinical use at Hacettepe University prior to this study. For research purposes, the system has been expanded to include structured capture of patient-reported outcomes, patient global impression of change, treatment protocol coding, home exercise adherence, and automated calculation of early response metrics. This is a 12-month prospective observational cohort study enrolling a minimum of 60 patients. Data are stored securely on the university's institutional network. Patients are anonymized using identification codes. The study is subject to Hacettepe University Ethics Committee approval and participant informed consent. Findings are expected to generate evidence supporting data-driven clinical decision-making in rehabilitation and to provide a feasibility foundation for a larger multi-center study.

Detailed description

The study addresses three research questions: (1) predictive power of early functional response for later clinical outcomes across four cascaded models (M1-M4), (2) classification of patient recovery profiles, and (3) measurement of clinical decision variation. System and methodological details reported in study supplement.

Primary outcome measures

• Feasibility: PROM Data Completeness [Time frame: Throughout the 12-month study period]
• Model M1: Session-Based Early Response → Session 12 [Time frame: Baseline (session 1) to session 12 (approximately 4-8 weeks)]
• Model M2: Month 1 Change → Month 3 Outcome [Time frame: Baseline to 3-month standardized assessment]
• Model M4: Month 1 Change → Month 6 Outcome [Time frame: Baseline to 6-month standardized assessment]

Secondary outcome measures (6)

• Model M3: Month 3 Change → Month 6 Outcome [Time frame: Baseline to 6-month standardized assessment]
• Recovery Profile Classification [Time frame: Baseline through session 12 (~4-8 weeks)]
• Clinical Decision Variation [Time frame: Throughout the 12-month study period]
• Feasibility: Clinician Acceptance [Time frame: At 3 months and 12 months]
• MCID Responder Rate [Time frame: Monthly from baseline to 12 months]
• Feasibility: Milestone Completion Rate [Time frame: Throughout the 12-month study period]

Eligibility criteria

Inclusion criteria

• Adults aged 18 years or older
• Hand or upper extremity pathology requiring rehabilitation, including but not limited to: flexor or extensor tendon injuries, peripheral nerve injuries or compression syndromes (including carpal tunnel syndrome, cubital tunnel syndrome), distal radius fractures, metacarpal or phalangeal fractures, joint injuries and instabilities, arthropathy (osteoarthritis, rheumatoid arthritis), trapeziometacarpal osteoarthritis, trigger finger, Dupuytren's disease, DeQuervain tenosynovitis, lateral epicondylitis and post-surgical upper extremity conditions
• Under clinical responsibility of the principal investigator at the Faculty of Physical Therapy and Rehabilitation, Hacettepe University
• Expected to attend minimum 8 rehabilitation sessions
• Able to provide written informed consent

Exclusion criteria

• • Active psychiatric illness precluding participation or completion of assessment tools

• Severe cognitive impairment precluding understanding of patient-reported outcome measures
• Literacy difficulties preventing self-completion of questionnaires
• Concurrent enrollment in another interventional clinical study
• Refusal to provide written informed consent

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model

Cohort

Study locations

Turkey (Türkiye) · 1 center

• Hacettepe University Faculty of Physical Therapy and Rehabilitation — Ankara

Identifiers

NCT: NCT07522060 · HU-HANDREHAB-2026

Primary sources (government registries)

• ClinicalTrials.gov (US NIH)

View this study on ClinicalTrials.gov ↗