Upper Cross Syndrome Rehabilitation Strengthening of the Dorsal Erector Muscles

NCT ID: NCT04540614

Last Updated: 2021-09-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-05-21

Study Completion Date

2021-06-04

Brief Summary

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

Detailed Description

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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.

Conditions

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Neck Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Intervention

70 participants receiving active comparator treatment plus experimental

Group Type EXPERIMENTAL

Strengthening exercises programme

Intervention Type OTHER

Strengthening exercises for Deep Cervical Flexors, Shoulder external rotators, scapular adductors and thoracic erector muscles

Control

70 participants receiving active comparator treatment

Group Type ACTIVE_COMPARATOR

Strengthening exercises programme

Intervention Type OTHER

Strengthening exercises for Deep Cervical Flexors, Shoulder external rotators, scapular adductors and thoracic erector muscles

Interventions

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Strengthening exercises programme

Strengthening exercises for Deep Cervical Flexors, Shoulder external rotators, scapular adductors and thoracic erector muscles

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Martín, Carlos García

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Carlos García

Role: PRINCIPAL_INVESTIGATOR

Fisiosesto

Locations

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Fisiosesto

Madrid, , Spain

Site Status

Countries

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Spain

Other Identifiers

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MartinCG

Identifier Type: -

Identifier Source: org_study_id

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