Effects of a Resistance and Stretching Training Program on Forward Head and Protracted Shoulder Posture Adolescents

July 14, 2014 updated by: Rodrigo Ruivo, Faculdade de Motricidade Humana

The Effects of Training and Detraining After an 8 Month Resistance and Stretching Training Program on Forward Head and Protracted Shoulder Postures in Adolescents

  • To evaluate the effects of a 32-weeks resistance and stretching training program applied in Physical Education classes on forward head and protracted shoulder Portuguese adolescents (15-17 years old).
  • To evaluate on adolescents submitted to strength and stretching exercises the effects of a 16-week detraining period after the end of the intervention protocol.

Study Overview

Detailed Description

A prospective, randomized and controlled study will be conducted over a 12 month period, with adolescents of two public secondary schools, in Lisbon.

At the beginning, a total of 275 adolescent students aged 15-17 years old will be evaluated with photogrammetry. The students will be screened by measuring the cervical (CV) and shoulder (SH) angle with photogrammetry. If the CV and SH angle were less than 50º and 52º respectively, the adolescent was considered to have forward head posture (FHP) and protracted shoulder (PS) and was selected to the study.

Participants will be excluded if their CV and SH angle was equal or higher than 50º and 52º respectively, if they had visual deficits, diagnosed balance disorders, musculoskeletal pathologies, such as a history of shoulder surgery, cervical or thoracic fracture, were non-ambulatory, displayed functional or structural scoliosis, or had excessive thoracic kyphosis.

After these the eligible students will be randomly assigned to the control or interventional group. The intervention group will begin a 32-week stretching and strengthening program to be performed in the last part of the Physical Education (PE) classes. The control group will only participate in the PE classes. Since the 32th week until the 48th week the experimental group will not follow the interventional training program and both groups will only participate in PE classes.

The program will be constituted by four strengthening exercises and three stretching exercises and is designed based on the assumption that the use of therapeutic exercise is effective in the correction of specific neck and shoulder postures. The training exercise protocol will be designed for the correction of the FHP and PS, targeting to the selective activation of lower trapezius, middle trapezius and rhomboids, to the lengthening of the pectoralis major, pectoralis minor and sternocleidomastoid and to the improvement of the deep cervical flexor function This program is going to be applied in the last 15-20 minutes of each PE class, twice a week, with the supervision and help of the PE teacher.

The postural assessment of the groups will be performed in the beginning and after 36 and 48-weeks intervention period.

Study Type

Interventional

Enrollment (Actual)

275

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

    • Cruz Quebrada-Dafundo
      • Lisbon,, Cruz Quebrada-Dafundo, Portugal, 1499-002
        • Technical University of Lisbon

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

15 years to 17 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

adolescents with 15-17 years old with cervical angle lower than 50º and the shoulder angle lower than 52º

Exclusion Criteria:

Participants were excluded if their CV and SH angle was equal or higher than 50º and 52º respectively, if they had visual deficits, diagnosed balance disorders, musculoskeletal pathologies, such as a history of shoulder surgery, cervical or thoracic fracture, were non-ambulatory, displayed functional or structural scoliosis, or had excessive thoracic kyphosis.

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: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Interventional program
The training protocol is constituted by 4 strengthening exercises (Side Lying External Rotation, Prone Horizontal Abduction with External Rotation, Y to I exercise and Chin Tuck) and 3 stretching exercises(one- Sided Unilateral Self Stretch Exercise, one-sided Unilateral Self Stretch Exercise, Static Sternocleidomastoid Stretch and Static Levator Scapulae Stretch
The postural correction training program was applied in the last 15-20 minutes of each PE class, twice a week, with the supervision and help of the PE teacher.
Active Comparator: Control group
The control group will only participate in the Physical Education classes
Only performed the physical education classes

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
change in postural angles (cervical and shoulder angle)
Time Frame: 36 and 48 weeks
We will assess the Cervical angle - the angle formed at the intersection of a horizontal line through the spinous process of C7 and a line to the tragus of the ear and the shoulder angle - The angle formed at the intersection of the line between the midpoint of the humerus and the spinous process of C7 and the horizontal line through the midpoint of the humerus.
36 and 48 weeks

Secondary Outcome Measures

Outcome Measure
Time Frame
the American Shoulder and Elbow Surgeons Standardized questionnaire
Time Frame: 36 and 48 weeks
36 and 48 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Rodrigo Ruivo, Master, University of Lisbon

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

October 1, 2012

Primary Completion (Actual)

May 1, 2013

Study Completion (Actual)

October 1, 2013

Study Registration Dates

First Submitted

July 11, 2014

First Submitted That Met QC Criteria

July 14, 2014

First Posted (Estimate)

July 15, 2014

Study Record Updates

Last Update Posted (Estimate)

July 15, 2014

Last Update Submitted That Met QC Criteria

July 14, 2014

Last Verified

July 1, 2014

More Information

Terms related to this study

Other Study ID Numbers

  • SFRH/BD/77633/2011

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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