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Clinical Trials/NCT05943340
NCT05943340Not yet recruitingNot Applicable

Effects of Proprioceptive Training on Shoulder's Muscle Mass After Distal Radius Fracture. Randomized Clinical Trial.

University of Malaga0 sites28 target enrollmentStarted: December 1, 2023Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
28
Primary Endpoint
Change in perception of Pain, referred to shoulder

Study Overview

Brief Summary

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

  • Study the relationship between shoulder muscle overload and shoulder pain.
  • Evaluate the effect of a proprioceptive program on pain and patient's satisfaction.

Intervention will be:

  • Control group: participants of this group are not going to receive any protocol of exercises during the immobilization period.
  • Experimental group: participants of this group are going to receive a protocol of proprioceptive shoulder exercises to do during the immobilization period.

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

Detailed Description

Distal radius fracture (DRF) in 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 to 6 weeks.

During the immobilization period, proximal structures suffer changes in mobility. Shoulder's ROM has to increased in order to compensate the immobilization of the wrist. Previous studies shown that there is a relation between time of immobilization and shoulder pain.

Shoulder pain can significantly affect daily living activities as driving, dressing or even eating. Also, pain does not appear only on it's own, but with other psychological factors as catastrophism, lower self-efficacy, fear of movement and avoidance. These factors could be crucial to predict disability in these patients, hence they should not be ignored during the rehabilitation process.

Our hypothesis is that the implementation of a proprioceptive shoulder exercise program during the period of immobilization may help and/or prevent shoulder pain secondary to immobilization.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Masking Description

Participants will be anonymized with a number and randomized with a web program (random.org)

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Adult (equal or more than 18 y/o).
  • •Suffering a distal radius fracture and being in the first week of the immobilization period.
  • •Agree and sign informed consent.

Exclusion Criteria

  • •Not had suffered a distal radius fracture and/or not being on the immobilization period.
  • •Suffer any mental, cognitive, neurological or musculoskeletal disorder.
  • •Previous injury or pathology of the shoulder diagnosed as fractures, instability, shoulder pain or capsulitis.
  • •Previous shoulder surgery.
  • •Have cervical pathology/impairment.

Arms & Interventions

Control group

No Intervention

Patients that are undergoing immobilization period after a distal radius fracture.

Experimental group

Experimental

Patients that are undergoing immobilization period after a distal radius fracture.

Intervention: Proprioceptive exercises (Other)

Outcomes

Primary Outcomes

Change in perception of Pain, referred to shoulder

Time Frame: Begining of the injury, baseline, 4 weeks and 3 months

Pain measured with Numerical Rating Scale (NRS). 0= no pain and 10=worst pain.

Change in function related with daily living activities

Time Frame: Begining of the injury, baseline, 4 weeks and 3 months

Measured with QuickDash. 11 items, 0= no disability and 100=total disability

Change in disability related with shoulder

Time Frame: Begining of the injury, baseline, 4 weeks and 3 months

Measured with Shoulder Pain and Disability Index (SPADI). 13 items, with 2 subscales (pain and disability). Pain subscale goes from 0-50 points and disability subscale goes from 0 to 80 points. Total punctuation is expressed as a percentage. More points indicates more disability.

Secondary Outcomes

  • Change in range of motion of the shoulder(Begining of the injury, baseline, 4 weeks and 3 months)
  • Change in shoulders muscle load(Begining of the injury, baseline, 4 weeks and 3 months)
  • Changes in kinesiophobia, fear of movement(Begining of the injury, baseline, 4 weeks and 3 months)
  • Changes in fear of movement(Begining of the injury, baseline, 4 weeks and 3 months)
  • Change in Perception of Quality of life(Begining of the injury, baseline, 4 weeks and 3 months)
  • Changes in catastrophizing pain(Begining of the injury, baseline, 4 weeks and 3 months)
  • Changes in self-efficacy related to pain(Begining of the injury, baseline, 4 weeks and 3 months)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Leire Cruz-Gambero

Principal Investigator

University of Malaga

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