Comparing Global Postural Re-education and Egoscue exercise in upper cross syndrome on neck pain, forward head and rounded shoulder posture
- Conditions
- Other soft tissue disorders,
- Registration Number
- CTRI/2023/10/059361
- Lead Sponsor
- KLE Academy f higher education and research
- Brief Summary
TITLE : Global Postural Re-education versus Egoscue exercises in Upper Cross Syndrome on neck pain, forward head and rounded shoulder posture - A Randomised Clinical Trial
Objective of the study : To determine and compare the effect of Global Postural Re-education and Egoscue exercise in Upper Cross Syndrome in terms of neck pain and functional ability using Neck disability index, forward head using kinovea app by measuring craniovertebral angle and rounded shoulder posture using pectoralis minor index
Inclusion criteria:
Clinically diagnosed cases of Upper cross syndrome with having atleast any one symptom from major criteria and one symptom from minor criteria
Participants aged between 20 to 50 years of either gender.
Participants willing to participate in the study and who can comprehend the commands.
Exclusion criteria :
any diagnosed muscle pathology or disease of soft tissues, fracture of spine, or spinal deformity
Diagnosed pathology like malignancy, and inflammatory disorders or vertebral artery insufficiency
Any history of spine disease, osteoporosis, blood diseases, and uncontrolled hypertension
History of any upper limb , lower limb, spinal or cardiothoracic surgery
Neuromuscular disorders, cognitive impairment and pregnancy
Undergoing any other recent therapeutic management within 3 months will be excluded.
Procedure
Group A - Global postural Re-education
Group B - Egoscue exercises
Both the groups will be given a common treatment in the form of Interferential therapy and Hot moist pack
Intervention will last for 35 minutes for each group
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 34
- Clinically diagnosed cases of Upper cross syndrome with having atleast any one symptom from major criteria and one symptom from minor criteria Participants aged between 20 to 50 years of either gender.
- Participants willing to participate in the study and who can comprehend the commands.
any diagnosed muscle pathology or disease of soft tissues, fracture of spine, or spinal deformity Diagnosed pathology like malignancy, and inflammatory disorders or vertebral artery insufficiency Any history of spine disease, osteoporosis, blood diseases, and uncontrolled hypertension History of any upper limb , lower limb, spinal or cardiothoracic surgery Neuromuscular disorders, cognitive impairment and pregnancy Undergoing any other recent therapeutic management within 3 months will be excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Cranio-vertebral angle(CVA) Pectoralis Minor Index(PMI) Pre- baseline at day 1 | Post baseline after 12 days of intervention
- Secondary Outcome Measures
Name Time Method Deep cervical flexor endurance test Tragus to wall test
Trial Locations
- Locations (1)
KAHER Institute of Physiotherapy
🇮🇳Belgaum, KARNATAKA, India
KAHER Institute of Physiotherapy🇮🇳Belgaum, KARNATAKA, IndiaDr Vaishnavi AghavPrincipal investigator9156948349vaishnaviaghav1999@gmail.com