Investigation of Spinal Health and Internet Addiction of Individuals Working Remotely

March 14, 2022 updated by: Aybüke Fanuscu, Hacettepe University

Low back pain and neck pain are common problems that affect people at certain times in their lives. These people constitute a significant part of the disease burden due to their recurrent complaints. People with low back and neck pain often seek medical attention. This situation causes individuals to apply to the hospital frequently and causes a serious cost at the social level.

When the risk factors for neck pain are examined, many factors such as genetics, sleep problems, smoking, obesity, sedentary lifestyle, poor posture, previous neck pain, trauma, back pain and poor general health cause neck pain to develop. Similarly, conditions such as age, obesity, and poor general health appear to be risk factors for low back pain. In addition to these risk factors, it has been reported that occupational factors such as long and sedentary working hours and unsuitable workplace conditions may also cause low back and neck pain. Fixed posture and prolonged sitting are thought to be risk factors for low back and neck pain, but opinions on this subject are not clear.

The COVID-19 pandemic has created a global crisis since 2019 and caused a change in the lifestyle of all people around the world. The World Health Organization (WHO) stated that social distance should be increased and face-to-face contact should be reduced to prevent the spread of the pandemic. For this reason, many institutions have decided to work remotely and trainings have been carried out remotely. The increasing teleworking style with the COVID-19 pandemic has led to an increase in the average screen time of individuals. It was reported that time spent on the Internet increased by 52% compared to the pre-pandemic period.

This study aims to investigate the relationship between increased teleworking hours and internet use during the pandemic period in individuals with low back or neck pain. Researchers think that postural changes that may occur with increased distance working time, increased fixed posture and asymmetrical loading may contribute to the uncertain relationship between low back and neck pain and posture.

Study Overview

Status

Not yet recruiting

Study Type

Observational

Enrollment (Anticipated)

48

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

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 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Individuals working remotely during the pandemic

Description

Inclusion Criteria:

  • Working online during the pandemic process,
  • Have a smart phone,
  • Agree to voluntarily participate in the research.

Exclusion Criteria:

  • Have a malignant condition,
  • Loss of function due to neurological or systemic disease,
  • Having had a surgical operation in the last 6 months,
  • Have an unhealed fracture,
  • Withdraw consent at any stage of 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

  • Observational Models: Cohort
  • Time Perspectives: Cross-Sectional

Cohorts and Interventions

Group / Cohort
Individuals Working Remotely
Individuals aged between 18-60 and working remotely, who volunteered to participate in the study, will form the study group.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation of Craniovertebral Angle
Time Frame: 5 minutes, in one assessment session.
Global Postural System (GPS) will be used for posture evaluation. GPS is a computerized photographic postural assessment system. It consists of a digital camera, a ruler frame, and a stable platform that allows for consistent landmark identification. The craniovertebral angle will be recorded, which provides the most relevant and reproducible data in the assessment of neck posture with GPS. The craniovertebral angle is the angle between a line drawn between the C7 vertebra and the tragus and a horizontal line drawn from C7
5 minutes, in one assessment session.
Evaluation of Sternocleidomastoideus Muscle Architecture
Time Frame: 5 minutes, in one assessment session.
Sternocleidomastoideus muscle will be architecturally evaluated by US using a 5-12 MHz linear probe (GE Logiq E5 ultrasound device) at rest and during muscle activation. Muscle thickness and pennation angle will be recorded.
5 minutes, in one assessment session.
Evaluation of Internet Addiction
Time Frame: 10 minutes, in one assessment session.
This evaluation will be carried out using the Kimberly Young Internet Addiction Questionnaire. The questionnaire consisting of 20 items; evaluate their dependencies in personal, professional and social functions. The questions are scored between 0 and 5 points. A total score between 0 and 30 indicates a normal level of internet use, total scores between 31 and 49 indicate the presence of mild addiction, a total score between 50 and 79 indicates the presence of a moderate level of addiction, and a total score of over 80 indicates the presence of severe internet addiction.
10 minutes, in one assessment session.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Evaluation of the Time Spent in Front of the Screen
Time Frame: 2 minutes, in one assessment session.
he time spent in front of the screen will be evaluated by questioning the average time spent by people on three different devices as computer, tablet and phone use.
2 minutes, in one assessment session.
Evaluation of Body Mass Index
Time Frame: 2 minutes, in one assessment session.
Body Mass Index (BMI), muscular and fat body weights will be assessed with TANITA BC420SMA (Tanita Corp, Tokyo, Japan). TANITA is a medically approved and reliable measuring device. It determines body composition by taking advantage of changes in bioelectrical resistance.
2 minutes, in one assessment session.
Evaluation of Low Back Disability
Time Frame: 5 minutes, in one assessment session.
It was developed to evaluate the level of functional loss in individuals with low back pain. The scale consists of 10 questions about pain intensity, self-care, lifting-carrying, walking, sitting, standing, sleep, degree of change in pain, travel and social life. Each question is scored between 0-5 points. The total score is evaluated out of 100. A high score means an increased level of disability.
5 minutes, in one assessment session.
Evaluation of Neck Disability
Time Frame: 5 minutes, in one assessment session.
The Neck Disability Questionnaire includes a total of 10 questions about pain, personal care, concentration, work, driving, and sleeping. Each question is scored between 0-5 points. 0-4 points means no disability, 5-14 points means mild disability, 15-24 points means moderate disability, 25-34 points means severe disability, 35 points and above means complete disability. The total score is evaluated out of 50.
5 minutes, in one assessment session.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Özlem Ülger, Professor, Hacettepe University
  • Study Chair: Yasemin Özel Aslıyüce, MSc, Hacettepe University
  • Study Chair: Dilara Onan, MSc, Hacettepe University
  • Study Chair: Müzeyyen Öz, MSc, Hacettepe University

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 (Anticipated)

March 20, 2022

Primary Completion (Anticipated)

June 20, 2022

Study Completion (Anticipated)

October 1, 2022

Study Registration Dates

First Submitted

October 16, 2021

First Submitted That Met QC Criteria

October 16, 2021

First Posted (Actual)

October 28, 2021

Study Record Updates

Last Update Posted (Actual)

March 15, 2022

Last Update Submitted That Met QC Criteria

March 14, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

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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