- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04540614
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
Intervention / Treatment
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.
Sponsor
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.
Clinical Trials on Neck Pain
-
Fatih TekinPamukkale UniversityCompletedChronic Neck Pain | Persistent Neck Pain | Neuroscience ApproachTurkey
-
Jeff Elias, MDRecruitingCancer of Head and Neck | Pain, Neck | Pain, FaceUnited States
-
Hacettepe UniversityRecruitingNeck Pain | Cervical Pain | Neck Pain, Posterior | Neck Muscle Issue | Cervical Pain, PosteriorTurkey
-
Riphah International UniversityCompletedCervical Pain | Mechanical Neck PainPakistan
-
Riphah International UniversityCompleted
-
Instituto Brasileiro de OsteopatiaCompletedNeck Pain | Pain, NeckBrazil
-
Ankara UniversityCompleted
-
Josue Fernandez CarneroCentro Universitario La SalleCompleted
-
Sakarya UniversityUnknown
-
Shanghai University of Traditional Chinese MedicineBeijing Hospital; Dongzhimen Hospital, Beijing; Traditional Chinese Medicine... and other collaboratorsNot yet recruiting
Clinical Trials on Strengthening exercises programme
-
Riphah International UniversityRecruitingEffects of Proximal Strengthening Exercises in Patellofemoral Pain Syndrome Among Basketball PlayersPatellofemoral SyndromePakistan
-
Riphah International UniversityCompletedUrinary IncontinencePakistan
-
Federal University of São PauloCompleted
-
Centre Hospitalier Universitaire DijonCompleted
-
Faculdade de Ciências Médicas da Santa Casa de...CompletedLow Back Pain, Mechanical | Low Back Pain, Postural | Lower Back Pain Chronic | Low Back Pain, Posterior CompartmentBrazil
-
Riphah International UniversityCompleted
-
Investigación en Hemofilia y FisioterapiaCompletedShoulder Injuries and DisordersSpain
-
University of FaisalabadRecruitingScapular DyskinesisPakistan
-
National Yang Ming UniversityRecruitingGlenohumeral Subluxation | Shoulder Instability Subluxation Bilateral | Shoulder SubluxationTaiwan