NCT05249673

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

87
On Track

Trial Health Score

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

Enrollment
32

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
6 days until next milestone

First Submitted

Initial submission to the registry

February 1, 2022

Completed
21 days until next milestone

First Posted

Study publicly available on registry

February 22, 2022

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 13, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 13, 2022

Completed
Last Updated

December 12, 2022

Status Verified

December 1, 2022

Enrollment Period

6 months

First QC Date

February 1, 2022

Last Update Submit

December 9, 2022

Conditions

Keywords

Text neck syndrome, REBA questionnaire, Turtle neck posture.

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

EXPERIMENTAL

global 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.

Other: global postural reeducation

neck stabilization training

ACTIVE COMPARATOR

Each 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.

Other: neck stabilization training

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.

Also known as: posture training
global postural reeducation

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.

neck stabilization training

Eligibility Criteria

Age20 Years - 40 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

Location

Study Officials

  • Muhammad Sanaullah, MS

    Study Principal investigator

    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

Locations