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Physical Activity in Lawyers: Factors Affecting Musculoskeletal Pain

2026年9月14日 更新者: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.

調査の概要

詳細な説明

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.

研究の種類

観察的

入学 (推定)

102

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

  • 名前:MEHMET DURAY, associate professor
  • 電話番号:+90 506 473 11 65
  • メール:mehmetduray@sdu.edu.tr

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

はい

サンプリング方法

確率サンプル

調査対象母集団

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.

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

コホートと介入

グループ/コホート
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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
International Physical Activity Questionnaire - Short Form (IPAQ):
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Nordic Musculoskeletal Questionnaire
時間枠: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
時間枠: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
時間枠: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
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

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研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2026年9月30日

一次修了 (推定)

2026年11月30日

研究の完了 (推定)

2027年1月30日

試験登録日

最初に提出

2026年9月14日

QC基準を満たした最初の提出物

2026年9月14日

最初の投稿 (実際)

2026年9月18日

学習記録の更新

投稿された最後の更新 (実際)

2026年9月18日

QC基準を満たした最後の更新が送信されました

2026年9月14日

最終確認日

2026年9月1日

詳しくは

本研究に関する用語

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

いいえ

IPD プランの説明

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

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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