Global Postural Reeducation Versus Neck Stabilization Training on Text Neck Syndrome.
Effects of Global Postural Reeducation Versus Neck Stabilization Training on Text Neck Syndrome
1 other identifier
interventional
32
1 country
1
Brief Summary
The study will be randomized control trial. The study will be conducted in Iqbal Mehmooda Trust Hospital. Group A will be treated with global postural reeducation. Group B will be treated with neck stabilization training. Non probability consecutive sampling technique will be used. Patient below 20-40 years, participants who use smart phones for 8 hours per day(guidelines), angle of forward head pasture above 15, screening picture tool. Neurological defects, trauma, tumor, shoulder injury, cervical disc disease. REBA questionnaire, NDI, Goniometry, NPRS will be used as a tool. The global postural reeducation will be applied on group A while neck stabilization training will be applied on group B. The aim of this study will be to compare the effects of of global postural reeducation and neck stabilization training on text neck syndrome.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jan 2022
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 26, 2022
CompletedFirst Submitted
Initial submission to the registry
February 1, 2022
CompletedFirst Posted
Study publicly available on registry
February 22, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 13, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
July 13, 2022
CompletedDecember 12, 2022
December 1, 2022
6 months
February 1, 2022
December 9, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
REBA questionnaire to measure body position on work station.
The Rapid Entire Body Assessment (REBA) was developed to "rapidly" evaluate the risk of musculoskeletal disorders (MSD) associated with certain job tasks. The change will be assessed from Baseline and end of treatment.
6 weeks
neck disability index to measure function of neck.
NDI questionnaire has been designed to give us information as to how your neck pain has affected your ability to manage in everyday life. It had 10 sections with total 50 scores. The test can be interpreted as a raw score, with a maximum score of 50, or as a percentage. 0 points or 0% means : no activity limitations , 50 points or 100% means complete activity limitation. The change will be assessed from Baseline and end of treatment.
6 weeks
Numeric pain rating scale to measure pain.
this scale is used for pain. Scale consists of 4 questions regarding actual pain level, zero indicates no pain and 10 indicates worst pain imaginable. The change will be assessed from Baseline and end of treatment.
6 weeks
Secondary Outcomes (1)
Neck Ranges (Flexion, Extension, Rotation and Side bending)
6 weeks
Study Arms (2)
global postural reeducation
EXPERIMENTALglobal postural reeducation (GPR) interventions will last 9 sessions, 1 hour each, with one-to-one supervision, once or twice a week according to the participant's needs. All participants will receive advice to follow written ergonomic suggestions and to repeat the exercises in the first physical therapy session at home twice a week for 15 minutes. Each group will get a home exercise program, which will differ according to the type of treatment received. Participants in the GPR group will execute one "posture" routine.
neck stabilization training
ACTIVE COMPARATOREach exercise session will be comprised of 10-minute warm-up exercises, 40-minute stabilization exercises, and 10-minute cool-down and stretching exercises, including neck and shoulder girdle muscles. The whole program will be carried out 3 days per week for 4 weeks.The participants will be asked to maintain the positions and contractions during the exercises and throughout the day as much as possible. The combination and progression of the exercises will be designed according to condition of the patient.
Interventions
GPR interventions will last 9 sessions, 1 hour each, with one-to-one supervision, once or twice a week according to the participant's needs. All participants will receive advice to follow written ergonomic suggestions and to repeat the exercises in the first physical therapy session at home twice a week for 15 minutes. Each group will get a home exercise program, which will differ according to the type of treatment received. Participants in the GPR group will execute one "posture" routine.
Each exercise session will be comprised 10-minute warm-up exercises, 40-minute stabilization exercises, and 10-minute cool-down and stretching exercises, including neck and shoulder girdle muscles. The whole program will be carried out 3 days per week for 4 weeks. performed. The participants will be asked to maintain the positions and contractions during the exercises and throughout the day as much as possible. The combination and progression of the exercises will be designed according to condition of the patient.
Eligibility Criteria
You may qualify if:
- Patient below 20-40 years
- Participants who use smart phones for 8 hours per day(guidelines)
- Angle of forward head posture above 15
- Screening picture tool
You may not qualify if:
- Neurological defects
- Trauma
- Tumor
- Shoulder injury
- Cervical disc disease
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Sana Mubarak
Lahore, Lahore,Punjab,Pakistan, 54000, Pakistan
Study Officials
- PRINCIPAL INVESTIGATOR
Muhammad Sanaullah, MS
Study Principal investigator
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 1, 2022
First Posted
February 22, 2022
Study Start
January 26, 2022
Primary Completion
July 13, 2022
Study Completion
July 13, 2022
Last Updated
December 12, 2022
Record last verified: 2022-12
Data Sharing
- IPD Sharing
- Will not share