Antigravity Treadmill With Alter G on the Postural Stability of Traumatic Lower Limb Injuries (ALTERG20)

Influence of Antigravity Treadmill With Alter G on the Postural Stability of Patients With Traumatic Lower Limb Injuries

This prospective randomised study aimed to test the investigators's hypothesis that anti-gravity treadmill therapy has beneficial effects on postural stability tests over a standard rehabilitation protocol in patients who have suffered traumatic injuries of the lower limb, demonstrating an improvement in the Biodex platform's values.

The total of 30 patients participated in this study (n=30). There were 15 subjects in control group and 15 in experimental group.

Study Overview

• Status: Not yet recruiting
• Conditions: Tendon Injuries; Lower Limb Injury; Ligament Injury; Muscle Injury; Injury Traumatic; Bone Injuries Joints
• Intervention / Treatment: Other: Alter G; Other: Parallel bars and Scale; Other: Standard rehabilitation protocol

Detailed Description

This prospective, randomised, controlled, longitudinal and triple-blind masked clinical design was performed in patients derived to the rehabilitation service of Fremap Sevilla Hospital after an laboral accident with surgery and not surgery traumatic injuries.

After that, participants were questioned about their personal data and the inclusion and exclusion criteria. All agreed to participate and provided signed informed consent prior to data collection.

Participants were allocated according to the inclusion and exclusion criteria into an intervention and a control group. The intervention was performed in two weeks. Patients were randomised into the intervention (anti-gravity treadmill) or control (standard protocol) rehabilitation group.

Previous data is taken from the "Postural Stability", "Stability Limits" and " m-CTSIB" tests on the Biodex Balance System SD platform.

The control group will perform the hospital's standard protocol for these injuries while the experimental group will also be added the anti-gravity treadmill in Alter G once a day.

At 2 week post-treatment, subjects were tested again. All patients were able to complete all rehabilitation sessions and balance tests.

Sample size assessment: accepting an alpha risk of 0.05 and a beta risk of 0.1 in a bilateral contrast, 15 subjects in each group are needed to detect a minimum difference of 15% between two groups, assuming that there are 2 groups and a standard deviation of 12%. A 10% rate of loss of insurance has been estimated.

Statistical analysis plan: the statistical analysis will be carried out using IBM-SPSS Statistics 24 software. The Kolmogorov-Smirnov test will be applied to test the distribution of the data. Student's t-test will be applied for paired variables when the data have a parametric distribution. The Mann-Whitney U test will be used to analyse data with a non-parametric distribution. The Chi-Squared will be used to compared qualitative variables. The confidence level used will be 95% (0.05) and the power of the study will be 90% (0.1).

• Study Type: Interventional
• Enrollment (Anticipated): 30
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Esther Melero; Phone Number: +34695756832; Email: esther_iya.emb@hotmail.com

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 25 years to 55 years (Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Age between 25 and 55
• Sex male and female
• Surgical or non-surgical subacute knee, ankle, and foot traumatic injuries

Exclusion Criteria:

• Vestibular pathology
• Important dysmetry
• Neurological pathology
• Acute inflammatory diseases.
• Important degenerative diseases.
• Autoimmune diseases.
• Severe visual deficits.
• Tumor pathology.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Triple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Alter G group; This group will perform the hospital's standard protocol for these injuries once a day during two weeks. They carried out the re-education of the gait (at the parallel bars) with a progressive load in scale controlled by the patient. Also, they carried out a re-education of the gait and progressive loading in the system Alter G (anti-gravity treadmill).	Other: Alter G; It is anti-gravity treadmill treatment on Alter G. They will start with a 30-50% body weight load during the first week that will be progressively increased to 50-70% during the second (5% more each day during the 10 sessions as far as possible). The slope will be 0% and the speed 2-3km/h the first week and 3-4 km/h the second. Treatment will be performed during 15 minutes for two weeks (10 sessions).; Other: Parallel bars and Scale; It is a re-education of the gait at the parallel bars with a progressive load in scale controlled by the patient during 10 minutes for two weeks.; Other: Standard rehabilitation protocol; It is the hospital's standard protocol for that injuries once a day for two weeks.
Other: Control group; This group will perform the hospital's standard protocol for these injuries once a day during two weeks. They just carried out the re-education of the gait (at the parallel bars) with a progressive load in scale controlled by the patient.	Other: Parallel bars and Scale; It is a re-education of the gait at the parallel bars with a progressive load in scale controlled by the patient during 10 minutes for two weeks.; Other: Standard rehabilitation protocol; It is the hospital's standard protocol for that injuries once a day for two weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Postural Stability test	The Postural Stability Test emphasizes a patient's ability to maintain center of balance. The patient's score on this test assesses deviations from center, thus a lower score is more desirable than a higher score.	Two weeks
LOS test	This test challenges patients to move and control their center of gravity within their base of sup- port. During each test trial, patients must shift their weight to move the cursor from the center target to a blinking target and back as quickly and with as little deviation as possible. The same process is repeated for each of nine targets. Targets on the screen blink in random order.	Two weeks
m-CTSIB test	This test provides an assessment of a patient's ability to integrate multiple senses with respect to balance and compensate when one or more of these senses are engaged. This test will be performed under 4 different conditions. It will be carried out bilaterally, first with the static platform and then with the unstable rubber surface to increase the difficulty.	Two weeks

Collaborators and Investigators

• Sponsor: FREMAP Mutual Insurance Company for Occupational Accidents and Diseases

Study record dates

Study Major Dates

• Study Start (Anticipated): June 1, 2022
• Primary Completion (Anticipated): July 10, 2022
• Study Completion (Anticipated): July 24, 2022

Study Registration Dates

• First Submitted: November 7, 2021
• First Submitted That Met QC Criteria: March 16, 2022
• First Posted (Actual): March 17, 2022

Study Record Updates

• Last Update Posted (Actual): March 17, 2022
• Last Update Submitted That Met QC Criteria: March 16, 2022
• Last Verified: March 1, 2022

More Information

Terms related to this study

• Keywords: gait; rehabilitation; lower limb; exercise therapy; body weight; postural balance; injury traumatic
• Additional Relevant MeSH Terms: Wounds and Injuries; Leg Injuries; Tendon Injuries
• Other Study ID Numbers: CTS954.EM1

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: No

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No