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Task-oriented Arm/Hand Skill Rehabilitation and Therapy Dose Dimensions in Subacute Spinal Cord Injury Rehabilitation

NCT05452707 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 47

Last updated 2023-04-06

No results posted yet for this study

Summary

The study is a multicenter longitudinal observational study. The therapy content and the therapy dosage of arm/skill training for patients with cervical spinal cord injury (SCI) will be observed for the primary objective. The aim is to get insight into the current therapy content and the current therapy dosage in arm/hand skill training, with the overall aim to optimize the arm/hand skill training. For the secondary objective, in addition to the patients with cervical SCI also, patients with paraplegia as a result of SCI are included. The aim is to assess the difference between the patient's perceived dose and the therapist's estimation of the therapy dose. This will give insight into the patient's and therapist's views on therapy dose; this information will contribute to optimizing therapy dose in exercise therapy in SCI. The third aim is a pilot study to explore the usability of evening reports in SCI rehabilitation.

Conditions

  • Spinal Cord Injuries

Interventions

OTHER

Observation and questionnaire of active therapy

There will be an observation of the usual care; no intervention will be added.

Sponsors & Collaborators

  • Adelante Zorggroep

    collaborator UNKNOWN

  • Universitaire Ziekenhuizen KU Leuven

    collaborator OTHER

  • University Ghent

    collaborator OTHER

  • Hasselt University

    lead OTHER

Principal Investigators

  • Annemie Spooren, Prof.Dr. · UHasselt

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-07-11
Primary Completion
2023-09-01
Completion
2023-09-01

Countries

  • Belgium
  • Netherlands

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05452707 on ClinicalTrials.gov