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Physical Activity in Lawyers: Factors Affecting Musculoskeletal Pain

2026년 9월 14일 업데이트: Aleyna Özdamar Yücel, Suleyman Demirel University

Determination of Factors Affecting Musculoskeletal Pain in Lawyers With Different Physical Activity Levels

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.

연구 개요

상태

아직 모집하지 않음

정황

상세 설명

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.

연구 유형

관찰

등록 (추정된)

102

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 연락처 백업

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

예

샘플링 방법

확률 샘플

연구 인구

The study population consists of volunteer lawyers registered with the Isparta Bar Association who are actively practicing law, have at least five years of professional experience, and are between the ages of 25 and 65.

설명

Inclusion Criteria:

  • To be registered with the Isparta Bar Association.
  • To be actively practicing law.
  • To have signed the "Informed Voluntary Consent Form" for participation in the research.
  • To have at least 5 years of professional experience.
  • To be between the ages of 25 and 65.

Exclusion Criteria:

  • Having a diagnosed serious neurological or rheumatological disease.
  • Having undergone major orthopedic surgery within the last 6 months.
  • Having a diagnosed psychological disorder.
  • Having cognitive-perceptual impairment severe enough to hinder understanding or answering questions-scoring below 24 on the Mini-Mental State Examination.

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

코호트 및 개입

그룹/코호트
Group 1: Those with a high level of physical activity
The study is designed as a descriptive, cross-sectional survey. Data will be collected using the Personal Information Form, the International Physical Activity Questionnaire-Short Form (IPAQ-SF), the Nordic Musculoskeletal Questionnaire, the Maslach Burnout Inventory, the Minnesota Satisfaction Questionnaire, and the Perceived Stress Scale. The study is based on voluntary participation and does not involve any intervention or treatment.
Group 2: Those with Low/Insufficient Physical Activity Levels
The study is designed as a descriptive, cross-sectional survey. Data will be collected using the Personal Information Form, the International Physical Activity Questionnaire-Short Form (IPAQ-SF), the Nordic Musculoskeletal Questionnaire, the Maslach Burnout Inventory, the Minnesota Satisfaction Questionnaire, and the Perceived Stress Scale. The study is based on voluntary participation and does not involve any intervention or treatment.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
International Physical Activity Questionnaire - Short Form (IPAQ):
기간: 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.
Day 1

2차 결과 측정

결과 측정
측정값 설명
기간
Nordic Musculoskeletal Questionnaire
기간: 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:

  1. Have you experienced pain, discomfort, or stiffness in this region within the last 12 months?
  2. Have you been prevented from performing normal work or household activities due to this pain within the last 12 months?
  3. Have you experienced pain or discomfort in this region within the last 7 days?

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,

Day 1
Minnesota Satisfaction Questionnaire
기간: 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

Day 1
Maslach Burnout Inventory
기간: 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

Day 1
Perceived Stress Scale
기간: 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.

Day 1

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2026년 9월 30일

기본 완료 (추정된)

2026년 11월 30일

연구 완료 (추정된)

2027년 1월 30일

연구 등록 날짜

최초 제출

2026년 9월 14일

QC 기준을 충족하는 최초 제출

2026년 9월 14일

처음 게시됨 (실제)

2026년 9월 18일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 18일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 14일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • SüleymanDU-122/19

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

IPD 계획 설명

The data for the primary and secondary objectives of the research will be compared after they are received.

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .