Distal Radius Fracture
Conditions
Keywords
Distal radius fracture, cross-education, immobilization
Brief summary
A single center randomized control study. Patients \>18 years with isolated distal radius fractures treated non-operatively will be randomly assigned to either the treatment group (exercise of contralateral well arm) or control group (standard fracture care and rehabilitation).
Detailed description
Distal radius fractures are common injuries, especially in the aging population. Fracture healing requires immobilization of the injury, which inevitably leads to muscle atrophy and joint stiffness. This strength lost during immobilization can be problematic in patients who are already de-conditioned at baseline. Previous research using healthy participants found that exercising a non-immobilized, well, arm helped attenuate muscle atrophy in the contralateral immobilized arm. The study aims to answer the following questions: Does exercise of the contralateral arm prevent muscle atrophy and weakness of the injured arm? Does exercise of the contralateral arm improve pain scores in the injured arm
Interventions
BEHAVIORALWell-arm Exercise
Patients randomized to the treatment arm will perform these exercises on the contralateral arm once daily for 3 months: wrist flexion and extension, ball or sock squeeze, wrist curls and biceps curls. Participants allocated to this study arm will be provided a print out of the exercises with detailed explanations and pictures of each exercise.
Sponsors
Henry Ford Health System
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)
Masking description
Patients will be randomized using an online randomization tool. Study folders will be placed in order and include the consent form and exercise sheet if randomized to the treatment group. Those randomized to the control group will be given an information sheet on distal radius fractures. Patients will be consented by an unblinded research assistant in order for the treating physician to remain blinded.
Intervention model description
Participants will be randomly assigned to one of two groups, treatment or no treatment. Randomizations will be balanced at random accrual points.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adults \>18 years with an isolated distal radius fracture treated non-operatively
Exclusion criteria
* Operative treatment, additional injures, previous injury to same arm, neuropathy or neuromuscular disease, dementia
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Grip strength | 3 months | Grip strength will be measured using a dynamometer at all clinic visits. |
| Forearm Circumference | 3 months | Forearm circumference will be measured at the widest point of the forearm, approximately 2cm distal to the elbow. This measurement will be taken at all clinic visits. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pain scores of injured arm. | 3 months | A visual analog scale (VAS) score will be collected at the first and all subsequent clinic visits. |
Other
| Measure | Time frame | Description |
|---|---|---|
| Wrist Range of Motion | 3 months | Range of motion of the injured wrist will be measured after the period of immobilization. |
Countries
United States
Outcome results
None listed