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National Survey of Chronic Occupational Pain in Thai Anesthesia Providers

2026년 8월 19일 업데이트: Mahidol University

Prevalence, Impacts, and Associated Factors of Chronic Occupational Pain Among Anesthesiologists and Nurses Anesthetists in Thailand: A National Survey

The purpose of this nationwide cross-sectional survey is to determine the prevalence, multidimensional impacts, and associated factors of chronic occupational pain among anesthesiologists and nurse anesthetists in Thailand. Due to the physically demanding nature of anesthesia practice-such as prolonged standing, awkward postures during airway management, and high-stress environments-work-related musculoskeletal disorders are highly prevalent but often underreported. This study aims to collect self-reported data via an anonymous online questionnaire to assess pain severity, specific anatomical locations, economic burdens (including absenteeism and presenteeism), and the overall impact on the health-related quality of life. Ultimately, the findings from this study will help establish a national evidence-based database to improve workplace safety, inform occupational health policies, and enhance the overall well-being of anesthesia providers in Thailand.

연구 개요

상태

아직 모집하지 않음

정황

상세 설명

Anesthesia providers, encompassing both anesthesiologists and nurse anesthetists, are highly susceptible to work-related musculoskeletal disorders (WMSDs) and chronic occupational pain. The nature of the profession requires prolonged static postures, repetitive movements, manual patient handling, and high-stress clinical management, all of which contribute to cumulative physical strain. Despite the critical role these professionals play in the healthcare system, comprehensive national data regarding the prevalence, severity, and multidimensional impacts of occupational pain within this specific population in Thailand remains highly limited.

This study is a nationwide, cross-sectional observational survey designed to evaluate the prevalence of chronic occupational pain and identify its associated factors among Thai anesthesia providers. The target population includes active anesthesiologists and nurse anesthetists aged 25 to 60 years who have been working in their current roles for at least six months.

The primary objective is to estimate the national prevalence of chronic occupational pain within this professional group. Secondary objectives include:

Assessing the severity, interference, and anatomical distribution of the pain using the validated Brief Pain Inventory-Short Form (BPI-SF Thai version).

Evaluating the impact of chronic pain on the health-related quality of life using the EuroQol 5-Dimension 5-Level (EQ-5D-5L) instrument.

Determining the economic burden associated with occupational pain, specifically focusing on healthcare utilization, absenteeism, and presenteeism (reduced work productivity).

Exploring the correlation between workplace exposures (e.g., specific clinical procedures, working hours, ergonomic factors) and the development of chronic pain.

Data collection will be conducted entirely through a structured, anonymous online questionnaire. The survey is designed with logic-branching to minimize respondent burden, ensuring that participants only answer questions relevant to their specific pain status. By gathering high-quality empirical data, this study aims to raise awareness among healthcare administrators, guide the development of targeted ergonomic interventions, and promote sustainable preventive strategies to secure the physical well-being and career longevity of anesthesia personnel.

연구 유형

관찰

등록 (추정된)

1800

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

건강한 자원 봉사자를 받아들입니다

예

샘플링 방법

비확률 샘플

연구 인구

The study population consists of actively practicing anesthesia providers, specifically attending anesthesiologists, anesthesia residents, and nurse anesthetists, who are currently working in healthcare facilities across Thailand.

설명

Inclusion Criteria:

  • Currently practicing as an anesthesiologist, anesthesia resident, or nurse anesthetist in a hospital in Thailand.
  • Aged between 25 and 60 years.
  • Have been working in their current clinical position and performing anesthesia-related tasks for at least 6 months.

Exclusion Criteria:

  • Currently on extended leave (e.g., long-term sick leave, maternity leave, or study leave) during the survey period.
  • Unwilling or unable to provide informed consent to participate in the study.

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
Thai Anesthesia Providers
Active anesthesiologists and nurse anesthetists, aged 25 to 60 years, who are currently practicing in Thailand and have been in their current roles for at least six months.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Prevalence of Chronic Occupational Pain
기간: At the time of survey completion (Day 1)
The proportion (%) of anesthesia providers experiencing chronic work-related pain, defined as pain lasting for at least 3 months. This is a binary (yes/no) determination collected via a self-reported structured questionnaire assessing the presence and anatomical locations of the pain; no severity scale or scoring system is used for this outcome.
At the time of survey completion (Day 1)

2차 결과 측정

결과 측정
측정값 설명
기간
Pain Severity and Interference
기간: At the time of survey completion (Day 1)
Assessed using the validated Thai version of the Brief Pain Inventory-Short Form (BPI-SF). It measures pain severity (scored from 0 = no pain to 10 = pain as bad as you can imagine) and the degree to which pain interferes with daily functions (scored from 0 = does not interfere to 10 = completely interferes). Higher scores indicate greater pain severity and interference.
At the time of survey completion (Day 1)
Health-Related Quality of Life
기간: At the time of survey completion (Day 1)
Evaluated using the Thai version of the EuroQol 5-Dimension 5-Level (EQ-5D-5L) instrument. It assesses five dimensions: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression, each rated on a severity scale from 1 (no problems) to 5 (extreme problems). Dimension responses are converted into a single index score using the Thai value set, ranging from a minimum of -0.42 (worse than death) to a maximum of 1.00 (full health). Lower index scores indicate poorer health status, while higher scores indicate better health status.
At the time of survey completion (Day 1)
Absenteeism Due to Pain
기간: At the time of survey completion (Day 1)
Measured by the self-reported number of work days missed due to pain over a specified recall period.
At the time of survey completion (Day 1)
Presenteeism Due to Pain
기간: At the time of survey completion (Day 1)
Measured by the estimated percentage of reduced work effectiveness while experiencing pain at work over a specified recall period.
At the time of survey completion (Day 1)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 수석 연구원: Suratsawadee Wangnamthip, M.D.Assoc. Prof., Mahidol university

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 8월 15일

기본 완료 (추정된)

2026년 11월 1일

연구 완료 (추정된)

2027년 1월 1일

연구 등록 날짜

최초 제출

2026년 8월 17일

QC 기준을 충족하는 최초 제출

2026년 8월 19일

처음 게시됨 (실제)

2026년 8월 21일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 8월 21일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 8월 19일

마지막으로 확인됨

2026년 8월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • 078/2569(IRB3)

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

아니요

IPD 계획 설명

Individual participant data will not be shared publicly to protect the privacy and confidentiality of the participants, in accordance with the Siriraj Institutional Review Board (SIRB) approval. Aggregated data and summaries will be published in a peer-reviewed journal.

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. .