crossed1: Crossed Education in Relation to Muscle Mass in Patients Operated of Clavicular Fracture

Sponsor
Universidad de La Frontera (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05810129
Collaborator
(none)
39
3
14.1

Study Details

Study Description

Brief Summary

The immobilization process after an operation or injury in the upper extremity causes a loss of muscle mass and strength of 0.2% and 1.3% per day, respectively. Currently, the use of cross-education, which is unilateral training in the uninjured limb, during the immobilization period, is expanding, demonstrating a magnitude of strength gain in the immobilized limb from 8% to 77% of the mean of strength of the trained limb. Despite the evidenced benefits of cross-education in unilateral injuries such as distal radius fracture, anterior cruciate ligament injury, and knee replacement, very little is known about this effect in shoulder immobilization after clavicle fracture.

Condition or Disease Intervention/Treatment Phase
  • Other: Cross-education training
  • Other: Cross-education training
N/A

Detailed Description

Objective: To determine the effectiveness of cross-education training through eccentric strength exercises compared to concentric-eccentric after the 6-week immobilization period and after 12 postoperative weeks in relation to muscle mass, strength, and functionality in patients operated of clavicular fracture.

Hypothesis: Cross-education training through eccentric strength exercises produces greater effects compared to concentric-eccentric training during the immobilization period and after 12 postoperative weeks, in relation to muscle mass, strength and functionality in patients operated for clavicle fracture.

Methodology: An experimental, randomized, single-blind study will be carried out, in which 39 men from 18 to 40 years of age will be recruited, who are awaiting surgery for clavicle fracture. They will be divided into three groups: control group (Standard Kinesic Therapy 12 weeks after immobilization of 6 weeks, n=13), concentric-eccentric group (concentric-eccentric strength training in the uninjured limb during the 6-week immobilization period + Standard Kinesics Therapy, n=13) and group eccentric (eccentric strength training on the uninjured limb during the 6-week immobilization period + Standard Kinesics Therapy, n=13).

Expected results: It is expected to observe a gain in muscle mass and strength in the trained limb and a maintenance/gain of muscle mass and strength in the groups that perform cross-training during the immobilization period, presenting the greatest benefit in the group that performs training eccentric force.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
39 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Masking Description:
single-blind study
Primary Purpose:
Treatment
Official Title:
Effects of Crossed Education in Relation to Muscle Mass, Strength and Functionality in Patients Operated of Clavicular Fracture
Anticipated Study Start Date :
Apr 28, 2023
Anticipated Primary Completion Date :
Jan 31, 2024
Anticipated Study Completion Date :
Jun 30, 2024

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control group

Men with clavicle fracture immobilized for 6 weeks + standard physical therapy for 12 weeks

Experimental: Concentric-eccentric group

Men with clavicle fracture who perform concentric-eccentric strength training on the uninjured limb during the 6-week immobilization period +Posterior Standard Kinesics Therapy.

Other: Cross-education training
Concentric-eccentric cross training in a 6-week immobilization period + 12-week standard kinesic therapy (2 times a week)
Other Names:
  • Concentric-eccentric
  • Experimental: Eccentric Group

    Men with clavicle fracture who perform eccentric strength training on the unaffected limb during the 6-week period of immobilization + Standard Kinesics Therapy.

    Other: Cross-education training
    Eccentric cross training in immobilization period of 6 weeks + Standard kinesic therapy of 12 weeks (2 times a week)
    Other Names:
  • Eccentric cross training
  • Outcome Measures

    Primary Outcome Measures

    1. Change in muscle thickness of the biceps brachii, triceps brachii and supraspinatus muscles by ultrasound. [before surgery, after 6 and 12 weeks postoperatively]

      Change in muscle thickness of the biceps brachii, triceps brachii and supraspinatus muscles by ultrasound.

    Secondary Outcome Measures

    1. Change in grip strength using a dynamometer and change in manual force at 90º elbow flexion, 45º shoulder flexion and 0º shoulder abduction [before surgery, after 6 and 12 weeks postoperatively]

      Change in grip strength using a dynamometer and change in manual force at 90º elbow flexion, 45º shoulder flexion and 0º shoulder abduction

    2. Upper and middle arm circumference change in both posterior arms [before surgery, after 6 and 12 weeks postoperatively]

      Upper and middle arm circumference change in both posterior arms

    3. Change in functionality using the Quick Dash questionnaire [before surgery, after 6 and 12 weeks postoperatively]

      Change in functionality using the Quick Dash questionnaire

    4. Change in relation to pain using the visual analogue scale [before surgery, after 6 and 12 weeks postoperatively]

      Change in relation to pain using the visual analogue scale

    5. Change in range of motion in elbow flexion, shoulder flexion, shoulder abduction, and rotations. [before surgery, after 6 and 12 weeks postoperatively]

      Change in range of motion in elbow flexion, shoulder flexion, shoulder abduction, and rotations.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 40 Years
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Men from 18 to 40 years old, diagnosed with radiographically verified clavicle fracture and awaiting surgical procedure. They have a body mass index of not less than 18.5 and not more than 29.9 kg/m2 and sign an informed consent.
    Exclusion Criteria:
    • Patients with previous injuries, pathological fracture or polytrauma

    • Patients who report pain, a history of rotator cuff tear or surgery in the non-injured upper extremity.

    • Patients with uncontrolled cardiovascular diseases.

    • Any history of neurological problems in the upper extremities.

    • Use of nutritional supplementation (leucine, glutamine, casein, whey-protein, fatty acids and creatine) and/or Hormonal Replacement Therapy.

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • Universidad de La Frontera

    Investigators

    • Principal Investigator: Gabriel Marzuca, MSc, PhD, Universidad de La Frontera. Temuco, Chile

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Gabriel Nasri Marzuca-Nassr, PhD, Universidad de La Frontera
    ClinicalTrials.gov Identifier:
    NCT05810129
    Other Study ID Numbers:
    • 057/23
    First Posted:
    Apr 12, 2023
    Last Update Posted:
    Apr 12, 2023
    Last Verified:
    Apr 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Gabriel Nasri Marzuca-Nassr, PhD, Universidad de La Frontera
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Apr 12, 2023