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Completed

NCT Number: NCT03044236

Effect of a Novel Stretching Technique on Shoulder Range of Motion and Voluntary Contraction in Overhead Athletes With Glenohumeral Internal Rotation Deficits "GIRD"

To examine and compare the effect of a novel stretching technique and traditional stretching on glenohumeral range of motion, strength, maximum voluntary contraction, pain, and subject satisfaction in overhead athletes with glenohumeral internal rotation deficits through a randomized clinical study.

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Key information

Age range

18 year–45 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Loma Linda U

Loma Linda, California, 92354, United States

About this study

To examine and compare the effect of a novel stretching technique and traditional stretching on glenohumeral range of motion, strength, maximum voluntary contraction, pain, and subject satisfaction in overhead athletes with glenohumeral internal rotation deficits through a randomized clinical study. The investigators hypothesize that this type of novel intervention will help subjects with GIRD to restore range of motion, experience less pain and maintain the strength and motor unit recruitment following the novel intervention. This will help us to assess the potential beneficial effect of such intervention and to fill the gap in knowledge and help health care professionals to adequately select the right treatment modality.

Independent Variable

  • Type of Intervention:
  • Traditional Stretching (Modified Sleep Stretch). VS
  • Novel Stretching (Active Shoulder Internal Rotation while Bridging) 2. Time
  • Pre VS post intervention Dependent Variables
  • Glenohumeral internal rotation ROM
  • Maximal glenohumeral external rotation isometric strength.
  • Mean motor unit recruitment (EMG) of the glenohumeral external rotator (infraspinatus) and internal rotators (pectoralis major and latissumus dorsi)
  • Pain
  • Subject satisfaction

Instrumentation :

  • Glenohumeral internal & external rotation ROM: will be measured at baseline and at week four-post intervention for all participants. We will use the digital inclinometer. Research by (Kolber et al.,2011 ) showed this instrument to be reliable with an intra-rater ICC =0.87 and inter-rater ICC =0.93
  • Electronic push/pull dynamometer: At the end feel ROM, and before ROM is measured, the therapist will apply the same amount of pressure to all subjects to ensure reliable/ valid ROM measurements.
  • Maximal Glenohumeral External Rotation Isometric Strength will be measured using a MicroFET2 handheld digital dynamometer. This device was shown to be reliable with an intra-rater ICC =0.85 and inter-rater ICC =0.85.
  • Maximum Voluntary Contraction: will be measured using a 44 Delsys Bagnoli portable surface electromyography (sEMG) system.
  • Pain: will be measured using the Numeric Pain Rating Scale (NPRS). The NPRS has shown to have a valid, reliable and appropriate for use in clinical practice

Procedures:

All participants will perform the static stretching (SS) conditions by themselves. The two stretching techniques will be home-based program.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants must be between the age of 18 and 45.
  • Perform overhead sports activities in the past 3 months.
  • Participants are required to display ≥ 20° less glenohumeral internal rotation ROM in their dominant shoulder compare to the non- dominate shoulder.
  • Participants will be included with or without pain during shoulder activities.

Exclusion criteria

  • Will exclude participants who are still recovering from previous surgery of the shoulder and elbow complex in the past 3 months, and currently receiving medical intervention for the shoulder.

Treatment and study plan

Stretching

Procedure

The novel stretching technique will be done on a supine position. subjects will be asked bridge as high as possible. After That, Participants will then flex their shoulder and elbow to 90°. Participants will use the other hand to push to the point of mild discomfort and simultaneously maintain contraction while progressing the stretch.

Primary outcomes

  1. Glenohumeral internal rotation ROM

    Time frame: Change from baseline at week 4

    The investigators will use the digital inclinometer

Secondary outcomes

  1. Maximal glenohumeral external rotation isometric strength

    Time frame: Change from baseline at week 4

    will be measured using a MicroFET2 handheld digital dynamometer

Other outcomes

  1. Mean motor unit recruitment (EMG) of the glenohumeral external rotator (infraspinatus) and internal rotators (pectoralis major and latissumus dorsi)

    Time frame: Change from baseline at week 4

    will be measured using surface electromyography (sEMG) system

  2. Pain will be measured using the Numeric Pain Rating Scale

    Time frame: Change from baseline at week 4

    will be measured using the Numeric Pain Rating Scale

  3. Subject satisfaction will be measured using the Subject satisfaction Form

    Time frame: Week 4

    will be measured using the Subject satisfaction Form

Sponsors and collaborators

Lead sponsor

Loma Linda University

Other

Registry information

Official study title

Effect of a Novel Stretching Technique on Shoulder Range of Motion and Maximum Voluntary Contraction in Overhead Athletes With Glenohumeral Internal Rotation Deficits: A Randomized Control Trial

Acronym: GIRD

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Feb 6, 2017
Registry last updated
Jun 11, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.