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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04089709
Other study ID # 11912
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date November 30, 2019
Est. completion date March 20, 2020

Study information

Verified date July 2022
Source Henry Ford Health System
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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).


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


Recruitment information / eligibility

Status Terminated
Enrollment 10
Est. completion date March 20, 2020
Est. primary completion date March 20, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Well-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.

Locations

Country Name City State
United States Henry Ford Hospital Detroit Michigan

Sponsors (1)

Lead Sponsor Collaborator
Henry Ford Health System

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Wrist Range of Motion Range of motion of the injured wrist will be measured after the period of immobilization. 3 months
Primary Grip strength Grip strength will be measured using a dynamometer at all clinic visits. 3 months
Primary Forearm Circumference 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. 3 months
Secondary Pain scores of injured arm. A visual analog scale (VAS) score will be collected at the first and all subsequent clinic visits. 3 months
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