Age-related Changes of Shoulder Muscles (SEMG)

November 22, 2016 updated by: Cristina Lirio Romero, University of Alcala

Age-related Changes in Activation Patterns of Shoulder Muscles

A cross-sectional descriptive study, in which the surface electromyographic activity of five shoulder muscles was compared in three populations: older adults, middle-aged adults and young adults. The evaluation of the electromyographic data offers a suitable foundation to understand aging process.

This supports that surface electromyography provide information about the aged shoulder muscles. Loss of functionality is suffered by a high percentage of older adults, which greatly limits their physical activity. In this sense, this paper presents findings that might be related with possible therapeutic approaches in subsequent studies.

Study Overview

Status

Completed

Conditions

Detailed Description

The purpose of the present work was to assess neuromotor abnormalities in aging shoulder. Twenty young adults (20-42), 20 middle-aged adults (43-67) and 20older adults (>68) were recruited. A comparative electromyography (EMG) study was performed on the upper and lower trapezius, middle deltoid, infraspinatus and serratus anterior. The EMG measurement (root mean square (RMS)) and onset time of isometric contractions were analyzed. Body mass index and strength were also tested.

Study Type

Observational

Enrollment (Actual)

60

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

20 years to 90 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Participants came from Madrid and Castilla La Mancha (Spain) and voluntarily attended the Unit of the Research Group "Physical Therapy in Women´s Health Processes" in the Department of Physical Therapy, University of Alcalá, and the Ocaña Senior Center.

Description

Inclusion Criteria:

  • Healthy subjects with no previously manifested symptoms in the shoulder joint and/or the neck during the past year,

Exclusion Criteria:

  • moderate or severe cognitive impairment, rheumatologic diseases, massive osteoarthritis, tumors, shoulder joint instability, circulatory disorders (hemophilia clotting problems) and dermatological problems exacerbated by contact with skin

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Ecologic or Community
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Group I: Older adults
healthy subjects older than 68 years old whose shoulder muscle are measured by surface electromyography
Group II: Adults
healthy subjects 43 to 67 years old, whose shoulder muscle are measured by surface electromyography
Group III: Young adults
healthy subjects 20 to 42 years old, whose shoulder muscle are measured by surface electromyography

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The mean Root Mean Square (RMS) value
Time Frame: 30 minutes
The electromyographic data were captured simultaneously on a PC by using the LabChart® software. Within the time interval from 2 to 4 seconds after contraction initiation a power spectrum analysis was performed together with the determination of RMS values. The mean RMS values were automatically obtained from the software
30 minutes
onset latency
Time Frame: 30 minutes
Start of contraction on the basis of 15% of RMS
30 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
maximal isometric voluntary contraction
Time Frame: 5 minutes
Using hand-held dynamometer
5 minutes
body mass index
Time Frame: 5 minutes
5 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Maria Tommes Lacomba, PhD, University of Alcala

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2014

Primary Completion (Actual)

March 1, 2015

Study Completion (Actual)

January 1, 2016

Study Registration Dates

First Submitted

November 20, 2016

First Submitted That Met QC Criteria

November 22, 2016

First Posted (Estimate)

November 28, 2016

Study Record Updates

Last Update Posted (Estimate)

November 28, 2016

Last Update Submitted That Met QC Criteria

November 22, 2016

Last Verified

November 1, 2016

More Information

Terms related to this study

Other Study ID Numbers

  • UAlcalaH

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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