Symptom Severity, Posture, Pain, and Physical Activity in Gastroesophageal Reflux Disease
NCT07643779
Behavior, Deglutition Disorders
View Trial DetailsNCT Number: NCT07827937
This study aims to determine the prevalence and distribution of musculoskeletal pain among lawyers registered with the Isparta Bar Association, specifically in relation to their varying levels of physical activity. The data obtained will help establish the relationships between physical activity levels, occupational factors, stress, and job satisfaction, thereby providing a foundation for developing personalized and preventive physiotherapy approaches for this specific population. Furthermore, the study will serve as a guiding resource for the ergonomic improvement of lawyers' working conditions and the formulation of occupational health policies.
H1: There is a statistically significant relationship between lawyers' physical activity levels and the frequency, distribution, and severity of musculoskeletal pain in various anatomical regions of the body.
H2: Physical activity level, perceived stress, occupational burnout, and job satisfaction levels are significant predictors of musculoskeletal pain among lawyers.
H3: There is a statistically significant difference between lawyers' sociodemographic and professional characteristics (duration of employment, daily time spent at a desk and using a computer, etc.) and their perceived stress and job satisfaction scores.
H4: Musculoskeletal complaints and functional limitations are significantly higher among lawyers experiencing high levels of perceived stress and occupational burnout compared to the group reporting low stress and burnout.
Trial opening soon.
Get Notified25 year–65 year
All sexes
Observational
This study will be conducted under the auspices of the Faculty of Health Sciences at Isparta Süleyman Demirel University, involving volunteer lawyers registered with the Isparta Bar Association. All stages of the study will be carried out in accordance with academic ethical guidelines and scientific research standards. An "Informed Voluntary Consent Form" will be obtained from all participating lawyers.
The research protocol consists of two main stages. In Stage 1, "Baseline Assessment and Physical Activity Classification," participants' physical activity levels will be determined using the International Physical Activity Questionnaire-Short Form (IPAQ-SF). Based on the obtained MET-minute/week scores, the sample will be divided into groups: "Group 1: Those with High Physical Activity Levels" and "Group 2: Those with Low/Insufficient Physical Activity Levels."
In Stage 2, the "Comprehensive Clinical and Psychosocial Assessment Protocol," data will be collected using the Personal Information Form, the Nordic Musculoskeletal Questionnaire, the Minnesota Satisfaction Questionnaire, the Maslach Burnout Inventory, and the Perceived Stress Scale. All data obtained during the study will be evaluated using statistical analysis methods, and the results will be reported in detail.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Day 1
The International Physical Activity Questionnaire-Short Form (IPAQ-SF) will be used to determine the participants' physical activity levels. The criterion for evaluating activity is based on the requirement that each activity be performed for a minimum of 10 minutes; a "MET-minute/week" score-representing energy expenditure relative to basal metabolic rate-is obtained by multiplying the duration (in minutes) by the number of days.
Time frame: Day 1
articipants' musculoskeletal complaints, the distribution of pain across body regions, and the impact of such pain on activities of daily living will be assessed using the Standardized Nordic Questionnaire (SNQ).
The questionnaire consists of items inquiring about nine anatomical regions: neck, shoulders, upper back, elbows, lower back, wrists/hands, hips/thighs, knees, and ankles/feet. For each region, participants are asked the following three key questions:
A binary (dichotomous) scoring system-"Yes" (1 point) or "No" (0 points)-is used for each question. Evaluations are conducted separately for each region based on frequency and percentage (%). Rather than calculating a total score,
Time frame: Day 1
The Minnesota Satisfaction Questionnaire (MSQ) will be used to determine the participants' levels of job satisfaction.
The scale is a short form consisting of 20 items and utilizes a 5-point Likert-type rating scale ranging from "1: Not at all satisfied" to "5: Very satisfied." The scale allows for the analysis of an individual's job satisfaction across three distinct dimensions:
Intrinsic Satisfaction (12 items): Refers to the satisfaction derived from the nature of the work itself (achievement, recognition, responsibility, utilization of abilities, activity, independence, social service, moral values, and authority) (items 1, 2, 3, 4, 7, 8, 9, 10, 11, 15, 16, and 20).
Extrinsic Satisfaction (6 items): Refers to the satisfaction stemming from the environmental conditions of the job (pay, advancement, supervision, company policies, coworkers, and social status) (items 5, 6, 12, 13, 14, and 19).
General Satisfaction (20 items): A score reflecting the individual's overall attitude towar
Time frame: Day 1
The participants' burnout levels will be assessed using the Maslach Burnout Inventory (MBI).
The scale consists of a total of 22 items and utilizes a 7-point Likert-type rating scale ranging from "0: Never" to "6: Every day."
The scale evaluates burnout across three distinct sub-dimensions:
Emotional Exhaustion (9 items): Reflects the individual feeling overloaded and emotionally depleted due to their work (items 1, 2, 3, 6, 8, 13, 14, 16, 20).
Depersonalization (5 items): Refers to the individual adopting a callous and emotionally detached attitude toward the people they serve (items 5, 10, 11, 15, 22).
Reduced Personal Accomplishment (8 items): Assesses the individual's perception of inadequacy in their work and a diminished sense of achievement (items 4, 7, 9, 12, 17, 18, 19, 21).
No total score is calculated for the scale; each sub-dimension is scored independently. High scores on the emotional exhaustion and depersonalization sub-dimensions, combined with low scores on the pers
Time frame: Day 1
The Perceived Stress Scale (PSS) will be used to determine the participants' stress levels and their perceptions of coping with stress over the past month.
The scale consists of a total of 14 items and utilizes a 5-point Likert-type rating scale ranging from "0: Never" to "4: Very often." The scale comprises two sub-dimensions:
Perceived Insufficient Self-Efficacy (7 items): Consists of items 4, 5, 6, 7, 9, 10, and 13, which assess the individual's perception of their ability to cope with stress (these items are reverse-scored).
Perceived Stress/Distress (7 items): Consists of items 1, 2, 3, 8, 11, 12, and 14, which measure the individual's reactions to sources of stress in their life.
The total score on the scale ranges from 0 to 56. A higher score indicates an increase in the individual's perceived stress level.
Contact information is provided by the study sponsor or research team.
Aleyna OZDAMAR YUCEL, MSc
CONTACT
MEHMET DURAY, associate professor
CONTACT
Suleyman Demirel University
Other
Determination of Factors Affecting Musculoskeletal Pain in Lawyers With Different Physical Activity Levels
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07643779
Behavior, Deglutition Disorders
View Trial DetailsNCT05708963
Back Pain, Behavior
New York, United States
View Trial DetailsNCT05326802
Back Pain, Behavior
New York, United States
View Trial DetailsNCT02945397
Behavior, Behavioral Symptoms
Bergen, Norway
View Trial Details