Occupational Health

9

Review clinical trials related to Occupational Health. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Work-Related Health Factors in General and Special Education Teachers

This cross-sectional study aims to compare work-related health outcomes between general education teachers and special education teachers. The study will assess burnout, occupational balance, perceived stress, musculoskeletal symptoms, pain characteristics, and general job satisfaction. Participants will complete an online questionnaire including sociodemographic and occupational characteristics, such as age, sex, teaching experience, working hours, and type of teaching assignment. Standardized self-report measures will be used to evaluate burnout, occupational balance, perceived stress, musculoskeletal symptoms, and pain-related characteristics. The study will examine whether teachers working in special education differ from general education teachers in terms of burnout, stress, occupational balance, musculoskeletal problems, and pain. The findings may help identify occupational health needs among teachers and support the development of preventive strategies for improving their well-being and working conditions.

Participants needed: 200
Trial details
Biological sex: AllType: ObservationalSponsor: Lokman Hekim UniversityUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

Aged 18 years or older. [+4]

Not currently working as a teacher during the data collection period (e.g., on l... [+2]

Status: Not yet recruiting

Workplace Violence and Safety Perception Among ENT Physicians in Turkey

This multicenter, cross-sectional survey study aims to evaluate the perceived level of safety and security against workplace violence among otolaryngology-head and neck surgery (ENT-HNS) physicians in Turkey. The study investigates the association between exposure to workplace violence and perceived safety, as well as the adequacy of institutional support mechanisms. Data will be collected through an anonymous online questionnaire distributed nationwide. The findings are expected to contribute to awareness and the development of preventive strategies and institutional safety policies for healthcare professionals.

Participants needed: 450
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Saglik Bilimleri UniversitesiUpdated: Apr 22, 2026Duration: 1 Day
Eligibility criteria

Licensed ENT-HNS specialist or resident physician [+2]

Physicians from other medical specialties [+1]

Status: Recruiting

HEalthCAre Workers' Health: a Transversal Evaluation

The research focuses on assessing the overall health of residents at the Cochin Port Royal hospital Group. * physical health * Mental health: detection of signs of anxiety, depression, eating disorders, substance abuse, etc. * Sexual health * Quality of medical care (dental, gynecological) * Knowledge of risk prevention, particularly infectious risks, in the workplace.

Participants needed: 2,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Assistance Publique - Hôpitaux de ParisUpdated: Apr 23, 2026Locations: 3
Eligibility criteria

Objection to the pseudonymous collection of data [+3]

Status: Recruiting

Impact of Stress First Aid for Workers in Substance Misuse Settings

Test the effectiveness of SFA adapted for the substance use outreach workforce compared to a no treatment control condition on social-support and burnout of HRWs in a cluster-randomized hybrid type I trial.

Participants needed: 500
Trial details
Age: 18-100Biological sex: AllType: InterventionalSponsor: University of Texas at AustinUpdated: Mar 3, 2026Locations: 1
Eligibility criteria

At least 18 years of age [+2]

Status: Not yet recruiting

French Military Firefighters to Assess Relationships Between Exposome and Health.

The aim of the study is to describe professional exposures and health events among French military firefighters (both active-duty personnel and veterans) and identify potential relationships between the exposome (the total history of occupational and personal exposures) and health status in these populations. The study is based on a self-administered questionnaire that collects retrospective and present information about exposures and health conditions.

Participants needed: 15,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Direction Centrale du Service de Santé des ArméesUpdated: Dec 8, 2025
Eligibility criteria

Active-duty or veteran military personnel from French Paris firefighter brigade. [+2]

Opposition to participate [+1]

Status: Not yet recruiting

Office Massage Effects on HRV and Stress

This study is a randomized controlled trial designed to investigate which of three short office massage types (head, neck/shoulder area, or hand) is most effective for reducing chronic stress in women who perform sedentary office work. Many sedentary female office employees experience long-term tension and work-related strain, which can affect the body's ability to recover. The investigators are testing whether a 15-minute massage, performed twice a week for four weeks, can help restore balance within the body. The investigators will evaluate the impact of these massages using Heart Rate Variability (HRV)-an objective measure that shows how well the body manages stress (autonomic nervous system balance)-as well as analyzing participants' self-reported levels of perceived stress, sleep quality, and overall well-being. Participants receiving massage will be compared to a control group engaging in quiet rest.

Participants needed: 140
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Riga Stradins UniversityUpdated: Dec 9, 2025
Eligibility criteria

Not listed

Status: Recruiting

Implementation of the ASCEND Training for Supervisors in Dutch Small and Medium-sized Enterprises (SMEs)

This cluster randomized controlled trial (cRCT) aims to evaluate the effectiveness of an in-person group intervention for workplace supervisors - Advancing Supervisors' Capacity for Mental Health at Work (ASCEND) - in Dutch Small and Medium-sized Enterprises (SMEs). The ASCEND intervention is designed to equip supervisors with the skills to: i) know when to support their workers; ii) how to direct workers to support, and iii) advocate for action on mental health at work. The primary objectives of this project are to: * Assess to what extent the novel, WHO-developed ASCEND intervention is effective in enhancing supervisors' confidence, responsiveness, mental health literacy, and SelfCare practices, and in reducing supervisor stigma towards mental health conditions within Dutch SMEs. * Evaluate the impact of the ASCEND intervention on employee outcomes, including mental health and work-related outcomes among supervisees (i.e., subordinates), as well as overall organizational absenteeism rates. * Identify barriers, facilitators, and key implementation and adoption indicators to support future opportunities for scaling up the ASCEND intervention in the context of Dutch SMEs. Researchers will compare two groups to evaluate the effectiveness of the ASCEND intervention. One group will receive the training (the intervention group), while the other group will receive the training after the final follow-up period (the control group). Data will be collected from both supervisors and their supervisees (i.e., subordinates) via online questionnaires at various time points. In addition, general organizational information, including absenteeism rates, will be gathered through a representative from each participating organization. To further explore the feasibility of scaling up the ASCEND intervention within the Netherlands, qualitative data will be collected through interviews and/or focus group discussions.

Participants needed: 148
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: VU University of AmsterdamUpdated: Nov 19, 2025Locations: 1
Eligibility criteria

Having 10 to 250 employees [+10]

Status: Recruiting

Non-Invasive System to Deliver Therapeutic Hypothermia for Protection Against Noise-Induced Hearing Loss

The goal of this interventional clinical study is to investigate the use of mild therapeutic hypothermia devices for preservation of sensory structures in the cochlea after noise exposure. The main aims of the study are: 1. To test the safety and best duration for use for a new hypothermia device. 2. To determine if the hypothermia device helps decrease noise-induced hearing loss in a group of firefighters. Participants will wear the mild therapeutic hypothermia therapy devices immediately after a fire service shift serially over a year. Researchers will compare results from those receiving the therapy to those from a control group (individuals receiving no therapy and a sham therapy).

Participants needed: 116
Trial details
Age: 18-55Biological sex: AllType: InterventionalSponsor: Restorear Devices LLCUpdated: Apr 2, 2025Locations: 1
Eligibility criteria

Adults aged 18-55 years old at the time of signing the consent form [+1]

Abnormal tympanometric findings [+7]

Status: Recruiting

A Randomized Controlled Evaluation of a Compassion-course for Healthcare Professionals

The aim is to investigate whether an internet-based compassion course of five modules contributes to reducing stress of conscience and work-related stress, increase the experience of professional quality of life and self-compassion in healthcare professionals.

Participants needed: 548
Trial details
Age: 20+Biological sex: AllType: InterventionalSponsor: Linnaeus UniversityUpdated: Mar 19, 2025Locations: 1
Eligibility criteria

Not listed