Upper Cross Syndrome Rehabilitation Strengthening of the Dorsal Erector Muscles

September 11, 2021 updated by: Martín, Carlos García

Upper Cross Syndrome Rehabilitation by Means of Habitual Treatment Plus Strengthening of the Dorsal Erector Muscles. Controlled Clinical Trial.

The purpose of this study is to determine which treatment is more effective for chronic neck pain associated with Upper Cross Syndrome.

Study Overview

Status

Completed

Conditions

Detailed Description

Patients will divided in two groups, control and intervention. Control Group will do exercises of strengthening of Deep Cervical Flexors, Shoulder External Rotators and Adduction of Scapulae.

Intervention group will do the same plus Strengthtening of Erector Thoracic.

Study Type

Interventional

Enrollment (Actual)

60

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Madrid, Spain, 28009
        • Fisiosesto

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

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Chronic neck pain for at least 3 months
  • 52º or less in the craniovertebral angle
  • 50º or less in the shoulder angle

Exclusion Criteria:

  • herniated disk, radiculopathy, diseases of the spine

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

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

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention
70 participants receiving active comparator treatment plus experimental
Strengthening exercises for Deep Cervical Flexors, Shoulder external rotators, scapular adductors and thoracic erector muscles
Active Comparator: Control
70 participants receiving active comparator treatment
Strengthening exercises for Deep Cervical Flexors, Shoulder external rotators, scapular adductors and thoracic erector muscles

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Craniovertebral angle
Time Frame: 0 week
tha angle formed by the horizontal line through C7 and the line formed between C7 and the tragus of the ear
0 week
Craniovertebral angle
Time Frame: 4 week
tha angle formed by the horizontal line through C7 and the line formed between C7 and the tragus of the ear
4 week
Craniovertebral angle
Time Frame: 8 week
tha angle formed by the horizontal line through C7 and the line formed between C7 and the tragus of the ear
8 week
Shoulder angle
Time Frame: 0 week
the angle formed by the horizontal line through C7 and the line formed between C7 and the acromion
0 week
Shoulder angle
Time Frame: 4 week
the angle formed by the horizontal line through C7 and the line formed between C7 and the acromion
4 week
Shoulder angle
Time Frame: 8 week
the angle formed by the horizontal line through C7 and the line formed between C7 and the acromion
8 week
VAS
Time Frame: 0 week
The Visual Analogue Scale 0 no pain 10 worst pain
0 week
VAS
Time Frame: 4 week
The Visual Analogue Scale 0 no pain 10 worst pain
4 week
VAS
Time Frame: 8 week
The Visual Analogue Scale 0 no pain 10 worst pain
8 week

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscle Strenght
Time Frame: 0 week
Muscle strenght tested by a hand held dynamometer
0 week
Muscle Strenght
Time Frame: 4 week
Muscle Strenght tested by a hand held dynamometer
4 week
Muscle Strenght
Time Frame: 8 week
Muscle strenght tested by a and held dynamometer
8 week
Muscle Activity
Time Frame: 0 week
Muscle activity tested by Portable EMG
0 week
Muscle Activity
Time Frame: 4 week
Muscle activity tested by Portable EMG
4 week
Muscle Activity
Time Frame: 8 week
Muscle activity tested by Portable EMG
8 week

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Carlos García, Fisiosesto

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 (Actual)

May 21, 2020

Primary Completion (Actual)

May 3, 2021

Study Completion (Actual)

June 4, 2021

Study Registration Dates

First Submitted

May 22, 2020

First Submitted That Met QC Criteria

September 1, 2020

First Posted (Actual)

September 7, 2020

Study Record Updates

Last Update Posted (Actual)

September 14, 2021

Last Update Submitted That Met QC Criteria

September 11, 2021

Last Verified

February 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • MartinCG

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

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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