Proprioceptive Training Following a Wrist Fracture

NCT ID: NCT06132646

Last Updated: 2023-11-15

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 28 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-01-07
• Study Completion Date: 2024-09-01

Brief Summary

The goal of this randomized clinical trial is to compare how a program of proprioceptive exercises for the wrist could influence in pain, functionality and quality of life in people that have suffered a wrist fracture. The main questions it aims to answer are:

• Evaluate the effect of a specific proprioceptive program on pain and functionality.
• Study the relationship between proprioception deficit and functionality.

Intervention will be:

• Control group: participants of this group are going to receive only standard rehabilitation program after wrist fracture.
• Experimental group: participants of this group are going to receive standard rehabilitation program after distal radius fracture and a specific proprioceptive program.

Researchers will compare control and experimental group to see if a implantation of a proprioceptive program for the wrist has benefits on pain, function and quality of life.

Detailed Description

Distal radius fracture (DRF) is one of the most frequent injuries in the upper limb, corresponding to 1/6 of the total fractures of the body. It appears mostly in >50 years old women (due to osteoporosis and menopause) but it is also frequent in middle age men as a consequence of a big trauma during sport activities or working. This injury can be treated conservative of surgically, but regardless of the treatment, it always has a period of immobilization between 3 and 6 weeks.

The term "proprioception" was firstly described by Sherrington in 1906 as "perception" of body position and movement. The presence and quantity of mechanoreceptors in the joint determine its proprioceptive capacity. In the 1990s, the presence of mechanoreceptors on the wrist was described, and subsequent studies allowed us to determine that the dorsal and ulnar ligaments of the wrist have a rich innervation of mechanoreceptors. With these findings, we can hypothesize various clinical applications, both for working on wrist proprioception in the early stages of proprioceptive reeducation without risking tissue damage and for neuromuscular work after fracture consolidation, with the goal of regaining fluid and balanced movement. Previous studies on the ankle, knee, and shoulder have shown that the implementation of a proprioceptive program in the rehabilitation process can improve traumatic instability and pain. Given that the wrist shares similarities with these joints in terms of proprioceptive innervation, we can hypothesize that a specific proprioceptive exercise program for the wrist may be beneficial in the recovery after a wrist fracture.

Conditions

Wrist Fractures; Pain

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Control group

Patients that had suffered a wrist fracture and are going to receive standard rehabilitation for the wrist.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Experimental group

Patients that had suffered a wrist fracture and are going to receive standard rehabilitation for the wrist.

Group Type: EXPERIMENTAL

Proprioceptive exercises

Intervention Type: OTHER

Specific proprioceptive exercises for the wrist that the patient has to do currently with standard rehabilitation.

Interventions

Proprioceptive exercises

Specific proprioceptive exercises for the wrist that the patient has to do currently with standard rehabilitation.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Adult (equal or more than 18 y/o).
• Suffering a wrist fracture and have passed immobilization period.
• Agree and sign informed consent.

Exclusion Criteria

• Not had suffered a wrist fracture, being in the immobilization period or not authorized by his/her orthopedic surgeon to start with rehabilitation.
• Suffer any mental, cognitive, neurological or musculoskeletal disorder.
• Previous injury or pathology of the upper limb affected.
• Previos surgery on the upper limb affected.
• Have cervical pathology/impairment.
• Suffering from blindness.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 90 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Malaga

OTHER

Sponsor Role: lead

Responsible Party

Leire Cruz-Gambero

Principal Investigator

Responsibility Role: PRINCIPAL_INVESTIGATOR

Other Identifiers

RaqCan342

Identifier Type: -

Identifier Source: org_study_id