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

Sponsor
Faculdade de Motricidade Humana (Other)
Overall Status
Completed
CT.gov ID
NCT02190331
Collaborator
(none)
275
1
2
12
22.9

Study Details

Study Description

Brief Summary

  • 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.

Condition or Disease Intervention/Treatment Phase
  • Other: Interventional program postural correction training
  • Other: Control Group physical education classes
N/A

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 Design

Study Type:
Interventional
Actual Enrollment :
275 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Treatment
Official Title:
The Effects of Training and Detraining After an 8 Month Resistance and Stretching Training Program on Forward Head and Protracted Shoulder Postures in Adolescents
Study Start Date :
Oct 1, 2012
Actual Primary Completion Date :
May 1, 2013
Actual Study Completion Date :
Oct 1, 2013

Arms and Interventions

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

Other: Interventional program postural correction training
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

Other: Control Group physical education classes
Only performed the physical education classes

Outcome Measures

Primary Outcome Measures

  1. change in postural angles (cervical and shoulder angle) [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.

Secondary Outcome Measures

  1. the American Shoulder and Elbow Surgeons Standardized questionnaire [36 and 48 weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years to 17 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Technical University of Lisbon Lisbon, Cruz Quebrada-Dafundo Portugal 1499-002

Sponsors and Collaborators

  • Faculdade de Motricidade Humana

Investigators

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

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Rodrigo Ruivo, Mr Rodrigo Ruivo, Faculdade de Motricidade Humana
ClinicalTrials.gov Identifier:
NCT02190331
Other Study ID Numbers:
  • SFRH/BD/77633/2011
First Posted:
Jul 15, 2014
Last Update Posted:
Jul 15, 2014
Last Verified:
Jul 1, 2014
Keywords provided by Rodrigo Ruivo, Mr Rodrigo Ruivo, Faculdade de Motricidade Humana

Study Results

No Results Posted as of Jul 15, 2014