- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06009081
Interventions For Neck Pain In Relation to Internet Usage
December 21, 2023 updated by: hazal genc, Istanbul Medipol University Hospital
A Comparıson Of Different Interventions For Neck Paın In Relation to Internet Usage Rates
After the rapid increase in the use of the Internet in the world, it has brought some negativities.People with internet addiction describe all the time they spend without internet as worthless and they want to be on the internet with an increasing desire.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Under all this information, the exercise program and walking programs that are easily added to people's lives in the study; The effects on stress and sleep levels were investigated by reducing neck pain symptoms in people with internet addiction.
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
-
-
None Selected
-
Istanbul, None Selected, Turkey, 34353
- Hazal GENÇ
-
-
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
- Child
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- 20 and 25 years old, have internet addiction
- have neck pain complaints for more than three months
- low category according to the International Physical Activity Index.
Exclusion Criteria:
- Participants who had mobility limitations and neurological problems -had spinal surgery, had a traffic accident in the last three months and were injured by whiplash injury mechanism- visual and hearing impairments,
- refused to participate in the study.
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 |
|---|---|
|
Experimental: postural exercise
An 8-week home exercise program consisting of neck exercises was applied for group 1.
The exercise program was carried out three times a week for eight weeks.
|
The exercises consisted of 4-way neck isometric exercises and stretching exercises for the activation of deep cervical flexors (chin tuck exercise) and combined with this exercise.
This protocol consisted of protocols studied in similar studies.
|
|
Active Comparator: aerobic exercise
An 8-week walking program was planned for Group 2 using pedometer feedback as a motivational tool.
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The walking program was carried out daily on a flat surface with a target of 7000 steps.
This goal is based on the American College of Sports Medicine reports on the minimum recommended levels of physical activity required to achieve health benefits, which includes several design elements.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
internet addiction scale
Time Frame: 8 weeks
|
Young's internet addiction scale is a 20-question self-report scale developed by Young.
There are answers to the questions as "Never", "Rarely", "Sometimes", "Often", "Very often", "Constantly".
According to the survey; He was defined as "Internet addict" when he scored 80 and above
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8 weeks
|
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Disability Index
Time Frame: 8 weeks
|
The Neck Disability Index is a frequently used scale to evaluate neck disability in the clinic.
Pain intensity assesses perceived neck pain in personal care, lifting, reading, headaches, concentration, work, driving, sleep, and leisure activities.
It was determined as "0" as the best and "50" as the worst
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8 weeks
|
|
Physical Activity Index
Time Frame: 8 weeks
|
The International Physical Activity Index, developed to measure the physical activity levels of individuals aged 15-65, asks questions about their physical activity in the last 7 days.It has three categories: Inactive (Category 1), Minimally Active (Category 2), Very Active (Category 3).
|
8 weeks
|
|
stress scale
Time Frame: 8 weeks
|
Perceived stress scale, this scale is used to measure stress perceptions.
In this scale, which has 14 questions in total, the answers are "Never", "Almost never", "Sometimes", "Quite often", "Very often".
In this test, the lowest "0" and the highest "56" points can be obtained; high values indicate the height of the stress perceived by the person .
|
8 weeks
|
|
Sleep Quality Index
Time Frame: 8 weeks
|
Pittsburgh Sleep Quality Index, developed by Buysse et al. in 1989, consists of 24 questions evaluating sleep status in the last 1 month.
A minimum score of 21 is obtained.
High scores indicate poor sleep quality
|
8 weeks
|
|
anxiety scale
Time Frame: 8 weeks
|
The Beck anxiety scale consists of four options as "Never", "Mild", "Moderate", "Severe" considering the questionnaire responses in the last week.
This scale, which has a score between 0-63 points, evaluates the symptoms of anxiety and is calculated as 63 points for the worst result.
If the results are lower than 21, it indicates mild anxiety, 22-35 indicates moderate anxiety, and higher than 36 indicates severe anxiety
|
8 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
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.
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)
August 18, 2023
Primary Completion (Actual)
October 18, 2023
Study Completion (Actual)
December 21, 2023
Study Registration Dates
First Submitted
August 18, 2023
First Submitted That Met QC Criteria
August 18, 2023
First Posted (Actual)
August 24, 2023
Study Record Updates
Last Update Posted (Actual)
December 22, 2023
Last Update Submitted That Met QC Criteria
December 21, 2023
Last Verified
December 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- E-10840098-772.02-4942
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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