Clinical Trials Directory

Trials / Completed

CompletedNCT02353442

Changes in Subjects With Posterior Capsule Tightness

Biomechanical and Neurophysiological Changes in Subjects With Posterior Capsule Tightness - Evaluation and Treatment

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
59 (actual)
Sponsor
Universidade Federal de Sao Carlos · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

To identify biomechanical and sensibility changes in people with posterior capsule tightness in people with and without shoulder pain.

Detailed description

Some studies have shown that posterior capsule tightness can be related with shoulder dysfunctions and kinematics alterations. This study will be divided in two studies. The purpose of study 1 will be to assess the scapular and humeral kinematics, the strength of the shoulder external rotators and the pressure pain threshold in subjects with posterior capsule tightness with and without shoulder pain. Study 2 will verify the effects of two different treatments in subjects with posterior capsule tightness and shoulder pain on the same variables of study 1. One-hundred subjects will participate in the first study and will be divided in 4 groups: Group 1 - 25 subjects with shoulder pain and posterior capsule tightness; Group 2 - 25 subjects with no shoulder pain and no posterior capsule tightness; Group 3 - 25 subjects with shoulder pain and no posterior capsule tightness; and group 4 - 25 subjects with no shoulder pain and no posterior capsule tightness. All subjects will complete the DASH and Shoulder Pain and Disability Index questionnaires. External and internal rotation range of motion, strength of the external rotators, scapular kinematics and humeral translations during arm elevation, and pressure pain threshold will be measured. For the second study 50 subjects with shoulder pain and posterior capsule tightness will be recruited. The subjects will be randomly divided in 2 groups: experimental group or control group. The experimental group will receive glenohumeral posterior mobilization, stretching of posterior capsule and strengthening of the shoulder external rotators. The control group will do ultrasound;, stretching for the upper trapezius and scapular squeezing. Both groups will receive intervention for 3x/week/4 weeks. All subjects will be supervised for one physiotherapist and same variables from study 1 will be analyzed at pre and post-intervention.

Conditions

Interventions

TypeNameDescription
OTHERPosterior shoulder mobilizationsA second investigator performed 5min of posterior capsule shoulder mobilization for the experimental group, 3times/week during 4 weeks.
OTHERExternal rotators strengtheningIndividuals performed 3x10 repetitions of external rotators strengthening in sidelying position 3times/week during 4 weeks.
OTHERPlacebo ultrasoundA second investigator performed 5min of placebo ultrassound for the control group, 3times/week during 4 weeks.
OTHERScapular squeezingIndividuals performed 3x10 repetitions scapular squeezing exercise 3times/week during 4 weeks.
OTHERUpper trapezius stretchingIndividuals performed 3x30s of upper trapezius stretching, 3times/week during 4 weeks.
OTHERPosterior Capsule StretchingIndividuals performed 3x30s of posterior capsule stretching, 3times/week during 4 weeks.

Timeline

Start date
2015-03-01
Primary completion
2016-08-01
Completion
2016-08-01
First posted
2015-02-02
Last updated
2017-03-21
Results posted
2017-02-15

Locations

1 site across 1 country: Brazil

Source: ClinicalTrials.gov record NCT02353442. Inclusion in this directory is not an endorsement.