NCT06185322

Brief Summary

Upper cross syndrome (UCS) is a common postural deformity characterized by a change in neck, torso and shoulder muscle activity and shoulder movement. UCS results in a shortening of the upper back and chest muscles as well as the muscles which provide movement to the shoulder blade. This is accompanied by weakness of the upper back muscles, shoulder blade stabilizor muscles and deep neck muscles. The resultant muscle imbalance leads to elevation of the shoulders, elongation of the neck and rounding of the back. The change in posture which occurs in UCS changes the biomechanics of the neck and upper back and can results in neck pain, adverse effects on daily activities and productivity. To date, studies have been done on treatment of elongation of the neck using muscle relaxation techniques and manipulation of the local structures. To date, there is no study which investigates the efficacy of a specific exercise program targeting the muscles affected by UCS. The aim of this study is to investigate the effects of UCS-specific exercises on neck-back pain, cervical posture, disability and quality of life.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
30

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2024

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 6, 2023

Completed
23 days until next milestone

First Posted

Study publicly available on registry

December 29, 2023

Completed
3 days until next milestone

Study Start

First participant enrolled

January 1, 2024

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2024

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

January 30, 2025

Completed
Last Updated

December 29, 2023

Status Verified

December 1, 2023

Enrollment Period

12 months

First QC Date

December 6, 2023

Last Update Submit

December 14, 2023

Conditions

Keywords

upper cross syndromeforward head positionpostureneck paincervicalgiapain ,cervicalposture balance

Outcome Measures

Primary Outcomes (1)

  • Visual analogue scale measurement of severity of neck pain

    A subjective measure of neck pain severity in the past week measured using a visual analogue scale from 0-100mm. 0mm signifies no pain, 100mm signifies the worst pain imaginable.

    Before physcial therapy treatment is commenced, after 10 sessions of physical therapy has been completed (2 weeks after commencement of therapy), three months after physical therapy has been completed.

Secondary Outcomes (6)

  • Neck disability index (NDI)

    Before physcial therapy treatment is commenced, three months after physical therapy has been completed.

  • Nottingham Health Profile (NHP)

    Before physcial therapy treatment is commenced, three months after physical therapy has been completed.

  • Goniometric measurement of cervical range of motion

    Before physcial therapy treatment is commenced, three months after physical therapy has been completed.

  • Occiput to wall distance and tragus to wall distance

    Before physcial therapy treatment is commenced, three months after physical therapy has been completed.

  • Radiographic evaluation of cervical posture and cervicothoracic alignment: Measure of cervical lordotic angle

    Before physcial therapy treatment is commenced, three months after physical therapy has been completed.

  • +1 more secondary outcomes

Study Arms (2)

Neck strengthening exercises group

ACTIVE COMPARATOR

10 sessions of physical therapy over two weeks.Each session will consist of 20 minutes of hotpack and transcutaneous electrical nerve stimulation and 10minutes of therapeutic ultrasound. Exercise sessions lasting 20minutes will consist of conventional neck isometric strengthening exercises under the supervision of a single physiotherapist. These exercises will be repeated 5 times each, twice daily. A brochure depicting each exercise,accompanied by a description,will be given to the patient.The patient will continue with the exercise program for 3 months and be reminded once a week via telephone.

Other: Physical therapy program with conventional neck strengthening exercises

Upper Cross Syndrome exercises group

EXPERIMENTAL

10sessions of physical therapy over two weeks.Each session will consist of 20minutes of hotpack and transcutaneous electrical nerve stimulation and 10minutes of therapeutic ultrasound.Exercise sessions lasting 20minutes will consist of stretching and strengthening exercises under the supervision of a single physiotherapist.Strengthening exercises for the deep neck flexors,upper and middle trapezius,serratus anterior will be performed by the patient.Ten repetitions of each exercise,three times daily will be recommended.Stretching exercises will include those for the upper trapezius,pectoralis majör,levator scapula,suboccipital and sternocleidemastoid muscles and izometric neck flexion-extension exercises.These will be repeated 5times each,twice daily.A brochure depicting each exercise,accompanied by a description,will be given to the patient.The patient will continue with the exercise program for 3 months and be reminded once a week via telephone.

Other: Physical therapy program with upper cross syndrome specific exercises

Interventions

Ten physical therapy sessions consisting of electrotherapy and upper cross syndrome -specific exercise program.

Upper Cross Syndrome exercises group

Ten physical therapy sessions consisting of electrotherapy and conventional neck strenthening exercises

Neck strengthening exercises group

Eligibility Criteria

Age30 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may not qualify if:

  • History of cervical spine trauma or surgery
  • Congenital postural deformity
  • A history of inflammatory arthritis
  • A diagnosis of torticollis, vertigo, pregnancy, vertebrobasilar insufficiency, heart failure, ischaemic heart disease, hypertension.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Oculocerebral hypopigmentation syndrome type PreusNeck Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Masking Details
The physiatrist who will initially assess, diagnose and collect outcome measures, will be blind to the study group of the patient. The patient will not know whether they are receiving the detailed exercise program or conventional exercise program.
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Associate Professor Doctor

Study Record Dates

First Submitted

December 6, 2023

First Posted

December 29, 2023

Study Start

January 1, 2024

Primary Completion

December 30, 2024

Study Completion

January 30, 2025

Last Updated

December 29, 2023

Record last verified: 2023-12