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Comparison of Rehabilitation Intervention, Supported by Telemedicine, With Standard Rehabilitation After Distal Radius Fracture.

H

Hospital Clinico Mutual de Seguridad

Status

Enrolling

Conditions

Distal Radius Fracture

Treatments

Device: Experimental

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This is a randomized clinical trial of two parallel arms, aiming to compare two rehabilitation interventions: an experimental intervention including telemedicine support and remote monitoring of compliance of usual indicated exercises, versus the usual protocol of indicated exercises supported by printed material (triptych) and without remote monitoring

Full description

Distal radius fracture is a common pathology. The surgical indication is given by the difficulty in obtaining fracture reduction or by the instability of the fracture. The long-term functional prognosis of the wrist depends largely on patients' adherence to the prescribed indications/exercises in the immediate postoperative phase.

This is a randomized clinical trial of two parallel arms, aiming to compare two rehabilitation interventions: an experimental intervention including telemedicine support and remote monitoring of compliance of usual indicated exercises, versus the usual protocol of indicated exercises supported by printed material (triptych) and without remote monitoring.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • distal radial fracture (A2 to C3 type according to the Orthopaedic Trauma Association classification system)
  • indication for standard rehabilitation post-surgery

Exclusion criteria

  • immediate post-surgery complication
  • multiple fractures or severe injuries
  • history of bone metabolism condition
  • illiterate
  • non-Spanish speaking
  • mental disorder
  • not familiar with electronic devices

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups

Experimental telemedicine
Experimental group
Description:
Patient's rehabilitation and compliance with the standard exercices will be guided and monitored through an ad hoc device developed specifically for this trial.
Treatment:
Device: Experimental
Control
Active Comparator group
Description:
Patient's rehabilitation and compliance with the standard exercices will be monitored in the usual manner, at the monthly visits to the physical therapy clinic
Treatment:
Device: Experimental

Trial contacts and locations

1

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Central trial contact

Felipe S Correa

Data sourced from clinicaltrials.gov

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