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National Survey of Chronic Occupational Pain in Thai Anesthesia Providers

19 août 2026 mis à jour par: 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.

Aperçu de l'étude

Description détaillée

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.

Type d'étude

Observationnel

Inscription (Estimé)

1800

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Sauvegarde des contacts de l'étude

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Oui

Méthode d'échantillonnage

Échantillon non probabiliste

Population étudiée

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.

La description

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.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

Cohortes et interventions

Groupe / Cohorte
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.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Prevalence of Chronic Occupational Pain
Délai: 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)

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Pain Severity and Interference
Délai: 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
Délai: 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
Délai: 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
Délai: 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)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Parrainer

Les enquêteurs

  • Chercheur principal: Suratsawadee Wangnamthip, M.D.Assoc. Prof., Mahidol university

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

15 août 2026

Achèvement primaire (Estimé)

1 novembre 2026

Achèvement de l'étude (Estimé)

1 janvier 2027

Dates d'inscription aux études

Première soumission

17 août 2026

Première soumission répondant aux critères de contrôle qualité

19 août 2026

Première publication (Réel)

21 août 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

21 août 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

19 août 2026

Dernière vérification

1 août 2026

Plus d'information

Termes liés à cette étude

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Description du régime IPD

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.

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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