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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03374059
Other study ID # KA 16/376
Secondary ID
Status Completed
Phase N/A
First received November 30, 2017
Last updated December 11, 2017
Start date September 1, 2016
Est. completion date September 1, 2017

Study information

Verified date December 2017
Source Baskent University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Objectives: The purpose of the study was to investigate the effects of exercise and life modification on pain and disability in "text neck".

Methods: Eighty-five participants were randomly divided into three groups: Exercise (n=29), Exercise+Life modification (n=28), and Control Group (n = 28). Pain intensity during rest, activity, and at night was evaluated with Visual Analogue Scale (VAS) and functional assessment was done by using Neck Disability Index at the beginning and at the end of 4 weeks.


Description:

Objectives: Smartphones or tablets have made an important place in our lives. However long-term use of technological tools causes postural disorders and neck pain called "text neck". The purpose of the study was to investigate the effects of exercise and life modification on pain and disability in "text neck".

Methods: Eighty-five participants with "text-neck" were randomly divided into three groups: Exercise (n=29), Exercise+Life modification (n=28), and Control Group (n = 28). First group received a home exercise program treatment for 4 weeks. Second group received life modification suggestions additional to home exercise treatment program. Control group did not receive any treatments. Pain intensity during rest, activity, and at night was evaluated with Visual Analogue Scale (VAS) and functional assessment was done by using Neck Disability Index at the beginning and at the end of 4 weeks.


Recruitment information / eligibility

Status Completed
Enrollment 85
Est. completion date September 1, 2017
Est. primary completion date September 1, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 30 Years
Eligibility Inclusion Criteria:

- Participants who were aged between 18 and 30, using technological devices as tablets and smartphones for more than 5 hours and having neck pain for more than 3 months were included in our study.

Exclusion Criteria:

- The exclusion criteria included those:

1. who had any diagnosed pathology for neck region diagnosed by MR or BT,

2. who had any shoulder pathology,

3. with any neck or shoulder surgery,

4. had whiplash syndrome,

5. had fibromyalgia, Myofasial Pain Syndrome or vascular pathology and

6. women who are breastfeeding.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Exercise program

Life modification


Locations

Country Name City State
Turkey Baskent University Ankara

Sponsors (1)

Lead Sponsor Collaborator
Baskent University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analogue Scale Pain intensity 4 weeks
Secondary Neck disability index Function 4 weeks
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