Yoga Exercises Applied With Two Different Technological Access

November 15, 2022 updated by: Buket AKINCI, Biruni University

Comparison of the Efficiency of Yoga Exercises Applied With Two Different Technological Access in White Collar Employees

Yoga, a form of exercise designed to bring balance and health to the physical, mental, emotional and spiritual dimensions of the individual, will benefit many white-collar workers by using popular technological environments to increase overall physical activity and well-being. The aim of this study is to examine the effects of yoga exercises applied with two different technological access in white-collar employees on musculoskeletal pain, fatigue, sleep quality, stress level, quality of life and work efficiency.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Considering the importance of the workforce and possible health problems in white-collar workers, it seems rational to implement health promotion practices in accordance with the digital age. There is no study in the literature examining the effectiveness of technology-based yoga on selected health outcomes in white-collar workers. Based on this shortcoming, the aim of this study is to examine the effects of yoga exercises applied with two different technological access in white-collar employees on musculoskeletal pain, fatigue, sleep quality, stress level, quality of life and work efficiency.

Study Type

Interventional

Enrollment (Actual)

22

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

      • Istanbul, Turkey
        • Biruni University

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

Description

Inclusion Criteria:

  • • Working full-time in the last 1 year in administrative, research-development, high-tech education, mind and brain power-based jobs

    • Speaks and writes Turkish
    • In order to join online sessions, participants should have internet access
    • All answers of the Physical Activity Preparation Survey should be selected as "No"

Exclusion Criteria:

  • • Uncontrolled hypertension and uncontrolled arrhythmia patience

    • Individuals who have undergone percutaneous transluminal coronary angiography or have a cardiac pacemaker
    • Individuals with severe neurological disease or serious respiratory disease
    • Previous stroke, myocardial infarction
    • Individuals who have undergone amputation
    • Individuals with major musculoskeletal problems
    • Individuals with injuries involving the lower extremity in the past 6 months
    • Pregnant or planning a pregnancy within 1 year
    • Breastfeeding
    • Use of sleeping pills or medication for psychological problems and/or shift workers

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: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Group A

Yoga exercises applied by video-conference method accompanied by a physiotherapist.

Evaluations and yoga exercises will be applied to the participants in this group through the "Zoom program". Yoga exercises were created with reference to studies in the literature. It will be applied for 8 weeks, 3 days a week and 40-45 minutes, at a time determined jointly by the physiotherapist and the participant (Table 1). Before starting the program, an informative broadcast will be made to the participants and groups of 6-8 people will be formed.

Yoga-based exercise training includes a warm-up and cool-down period for beginners
Active Comparator: Group B
Yoga exercises performed asynchronously accompanied by videos. Exercise videos will be broadcast to the participants in this group through the "YouTube program". The shooting of the exercise videos will be completed in advance and uploaded to a channel opened on YouTube. All posts made in this channel will only be open to individuals participating in the research during the duration of the study. Yoga exercises were created with reference to studies in the literature. It will be applied for 8 weeks, 3 days a week and 40-45 minutes. Participants will be able to access the exercise videos at a time they want (Table 2). Participants will be encouraged to achieve weekly targeted training sessions and to keep an exercise diary.
Yoga-based exercise training includes a warm-up and cool-down period for beginners

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
physical activity level
Time Frame: 8 weeks
International Physical Activity Questionnarie -Short Form: This measure assesses the types of intensity of physical activity and sitting time that people do as part of their daily lives are considered to estimate total physical activity in MET-min/week and time spent sitting.
8 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
musculoskeletal pain level
Time Frame: 8 weeks
Nordic Musculoskeletal Questionnaire: The questionnaire consists of four parts. In the first part, first name, last name, date of questioning, gender, date of birth, body weight, length of stature, dominant side, how many years/months has he been working in the current job and how many hours worked on average in a week are recorded. In the second part the last 12 months, individuals in nine different body regions (neck, shoulder, back, elbow, waist circumference, wrist/hand, hip/thigh, knee, and ankle/foot) with the presence of pain or discomfort experienced the pain of blocking the Activity Status is questioned. The third section nine different body areas of pain or discomfort experienced in the last 7 days individuals in the presence and in the final chapter, an individual one of these areas which, when applied to the physician because of pain or discomfort in questioned.
8 weeks
fatigue severity.
Time Frame: 8 weeks
The Fatigue Severity Scale: It is shown as the best example among one-dimensional decimals. It consists of a total of 9 questions, and each question on the scale is scored from 1 (I don't agree at all) to 7 (I completely agree). The total score of the scale dec from 9 to 63. The fact that the total score that can be obtained from the scale is 36 or higher indicates severe fatigue.
8 weeks
sleep quality
Time Frame: 8 weeks
Pittsburgh Sleep Quality Index: The scale evaluates the individual's sleep quality, amount of sleep and the presence of sleep disorder. There are 19 questions answered by the individual himself and 5 questions answered by the individual's roommate in the scale, which consists of 24 questions in total. However, when calculating the total score of the scale, the questions answered by the roommate are not included in the calculation. The scoring includes 18 items and 7 components: subjective sleep quality, sleep latency (delay), sleep duration, habitual sleep efficiency, sleep disturbance, use of sleeping pills, daytime dysfunction. Each item is scored between 0-3. The total score of the scale is calculated by the sum of the scores from the seven components, and the total score ranges from 0 to 21 points. A total score of 5 or more indicates poor sleep quality.
8 weeks
perceived stress
Time Frame: 8 weeks
Perceived Stress Index: The Perceived Stress Scale will be used to evaluate the stress level of the participants. The scale was developed to identify the source of stress and the level of perceived stress. The questions in the scale should be answered by taking into account the feelings and thoughts in the last month. It consists of 14 items in total and each item is rated with a 5-point Likert-type scale. High scores obtained from the scale indicate that the perception of stress is high.
8 weeks
quality of life of the participants
Time Frame: 8 weeks
Short Form-36 will be used to assess the participants' quality of life. The scale developed by Corporation consists of 36 items and 8 sub-dimensions. Sub-dimensions of the scale; physical function (10 items), social function (2 items), role limitations due to physical functions (4 items), role limitations due to emotional problems (3 items), mental health (5 items), energy/vitality (4 items), pain (2 items) and general perception of health (5 items). Each item in the scale should be answered considering the last four weeks. Instead of a single total score from the scale, each sub-dimension is scored separately. The sub-dimension score ranges from 0 to 100. 0 points indicate poor health and 100 points indicate good health.
8 weeks
work efficiency
Time Frame: 8 weeks
Endicott Productivity at Work scale: The scale consists of 25 items and besides these items, the number of hours the individual has to work, the number of hours he has worked, and if he has worked less than necessary, the reason for this is questions. The 25 items related to work efficiency are never (0), rarely (1), sometimes (2), often (3), or almost always (4), depending on how often the individual's behavior, emotion, or attitude has been seen in the previous week. as a score. The lowest total score that can be obtained from the scale is 0 and the highest total score is 100. A high score indicates low work efficiency.
8 weeks

Collaborators and Investigators

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

Investigators

  • Study Chair: Buket Akıncı, Biruni 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 (Actual)

April 1, 2022

Primary Completion (Actual)

October 15, 2022

Study Completion (Actual)

October 15, 2022

Study Registration Dates

First Submitted

March 17, 2022

First Submitted That Met QC Criteria

March 17, 2022

First Posted (Actual)

March 28, 2022

Study Record Updates

Last Update Posted (Actual)

November 16, 2022

Last Update Submitted That Met QC Criteria

November 15, 2022

Last Verified

November 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

product manufactured in and exported from the U.S.

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.

Subscribe