Clinical Trials Directory

Trials / Unknown

UnknownNCT04820114

Proprioception and Multi Sensory Training After DRF

The Role of Proprioception and Multi Sensory Training on Recovery and Patient Satisfaction After Distal Radius Fracture. Randomized Control Trial.

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
62 (estimated)
Sponsor
University of Malaga · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Distal radius fracture is the most common upper extremity fracture with peak incidence among older women after the fifth decade of life. Proprioception is one constituent of a complex Sensory motor control process. Proprioception requires the reception and central integration of incoming afferent signals. Although various sensory and motor deficits have been correlated with significant functional impairment after wrist trauma, limited research exists on the effects of proprioception and multi sensory training after distal radius fracture.

Detailed description

A randomized, controlled, single-center, double-blind, clinical trial, with 1:1 allocation ratio, will be carried out involving patients diagnosis of distal radius fracture (aged 18 years and above). Both assessor and statistician will remained blinded. Standard rehabilitation program for distal radius fracture treatments will received for both the control and experimental groups for a period of 12 weeks. The experimental group, in addition, will received a proprioceptive training program during the same intervention period, which will be conducted twice weekly (24 sessions). The severity of pain with activity will be measured according to the visual analog scale (VAS). PRWE questionnaire will be used to measure upper extremity function. Patient's occupational performance will be measured with the Canadian Occupational Performance Measure (COPM) and proprioception with Joint position sense (JPS) and force sense (FS) testing. All outcome measures will be collected at baseline, immediately following the intervention at 3 weeks and at 12 weeks following the end of the intervention. Participation in the study will be voluntary and patients will be included if they satisfied specific inclusion criteria. All procedures will be follow in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration. All participants will sign a written informed consent in accordance with guidelines approved by the local ethics committee.

Conditions

Interventions

TypeNameDescription
OTHERProprioceptive wrist exercisesExercises for recognition of writs position and thumb force sense.
OTHERWrist exercisesPassive and active exercises for improve range of motion in flexion, extension, ulnar and radial deviation

Timeline

Start date
2021-04-01
Primary completion
2021-06-01
Completion
2022-01-01
First posted
2021-03-29
Last updated
2021-04-30

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT04820114. Inclusion in this directory is not an endorsement.