- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05048992
Effects of ElDOA and Post-Facilitation Stretching Technique on Pain and Disability in Patients With Text Neck Syndrome
April 21, 2022 updated by: Riphah International University
In this modern era, Text Neck is a new term used to describe neck pain and associated damage caused by continuous flexed posture due to excessive use of smartphones for a long time.
The term text neck was first introduced by Dr. Dean L. Fishman, who is US based chiropractor.
Text neck can also be described as overuse syndrome caused by repetitive stress on neck due to prolonged flexion.
There is coordinated work between cervical spine and surrounding structure such as muscles, ligament, nerves and bones.
In addition, any nerve compression at cervical spine leads to radiating pain in neck, shoulder and arm.
Previous literature reported use of cell phone is very common in population of 18 to 44 years of age.
Seventy nine percent (79%) population have smartphone with them all the time.
Technology has become essential part of modern lifestyle.
Sustained flexed posture forces the head to exert weight on neck of varying degrees.
Weight of neutral head is 10 to 12 pounds and increases 6 times 1 inch forward movement of head.
Children are at higher risk because of their large head size.
This study will be a Randomized clinical trial with objective to reduce neck pain and disability in patients with text neck syndrome.
Two groups will be designed, in one group ElDOA (n=20) and in other group post facilitation technique (n=20) will be applied.
Patients will be recruited into two groups by consecutive sampling by non-replacement lottery method with equal no. of chits.
Patients will be assessed by Numeric pain rating scale (NPRS), Neck disability index (NDI), smartphone addiction scale before and after treatment.
Both groups will receive heating pad as common treatment first after that group A will be treated with ELDOA and group B will be treated with Post-facilitation.
Session of 6 weeks with 3 days per week will be conducted.
After that post treatment assessment will be done.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
40
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Punjab
-
Lahore, Punjab, Pakistan, 54000
- Safi Hospital Faisalabad
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 35 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
• Neck pain without unilateral UE symptoms
- Age 18-35 years
- Subjects using Phone since past 1 year
- Neck disability index (NDI) score >10 points
- Participants able to understand and fill the questionnaire in English
Exclusion Criteria:
• Subjects having any congenital cervical condition
- Subjects having traumatic cervical condition such as whiplash injury within the past 6 weeks
- History of spinal tumors, spinal infection, cervical spine fracture, or previous neck surgery
- Subjects with cervical radiculopathy
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: ELDOA method
Twenty (20) patients will be treated with ELDOA method
|
group A will receive
|
|
Active Comparator: Post-facilitation stretching
Twenty (20) patients will be treated with Post-facilitation stretching technique.
|
Group B will receive
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric Pain Rating Scale (NPRS)
Time Frame: 6 weeks
|
will be used for pain measurement.
It is a uni-dimensional 11 point scale (0-10) with measure of pain intensity.
|
6 weeks
|
|
Neck disability index (NDI)
Time Frame: 6 weeks
|
) will be used to assess neck disability.
It consists of 10 sections and each section carries 5 marks.
0 indicate no activity limitation and 5 indicates complete activity limitation.
|
6 weeks
|
|
Smartphone addiction scale (SAS)
Time Frame: 6 weeks
|
will be used to assess smartphone addiction.
It is self-reporting scale consist of 6 factors and 33 items.
Score ranges from 33 to 198 and higher the score greater the degree of addiction.
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Muhammad Salman Bashir, PhD, Riphah International University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
General Publications
- Lee JI, Song HS. The correlation analysis between hours of smartphone use and neck pain in the Gachon university students. Journal of Acupuncture Research. 2014;31(2):99-109.
- Neupane S, Ali U, Mathew A. Text neck syndrome-systematic review. Imperial Journal of Interdisciplinary Research. 2017;3(7):141-8
- Vate-U-Lan P. Text neck epidemic: a growing problem for smart phone users in Thailand. International Journal of the Computer, the Internet and Management. 2015;23(3):551-6.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
October 30, 2021
Primary Completion (Actual)
March 15, 2022
Study Completion (Actual)
March 30, 2022
Study Registration Dates
First Submitted
September 13, 2021
First Submitted That Met QC Criteria
September 13, 2021
First Posted (Actual)
September 17, 2021
Study Record Updates
Last Update Posted (Actual)
April 22, 2022
Last Update Submitted That Met QC Criteria
April 21, 2022
Last Verified
April 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- RCE/Lhr/0116 Maryam
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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