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Active, not recruitingNCT07786584YOGA-CAREUpdated Aug 26, 2026

Burnout and Well-Being in Healthcare Workers Participating in Workplace Yoga

An observational study in Burnout, Occupational Burnout and Yoga Therapy, sponsored by IRCCS Centro Neurolesi Bonino Pulejo. Active, not recruiting at 1 site in Italy. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-26.

Primary conditionBurnout, ProfessionalRegistry: Burnout, PsychologicalReclassifiedWhy we changed it
Registry
Burnout, Psychological — the first condition term the registry derived for this study.
ClinicalTrials.gg
Burnout, Professional
Why
  1. The study's listed conditions name Burnout, Professional, a narrower term within Burnout, Psychological.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by IRCCS Centro Neurolesi Bonino Pulejo · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
70
Ages
18 Years and older
Sex
All
01

Study summary

This study aims to evaluate changes in burnout, perceived stress, coping strategies, anxiety, depression, and psychological well-being among healthcare workers participating in a workplace yoga program.

Healthcare professionals are frequently exposed to high emotional demands, workload pressure, irregular shifts, and substantial clinical responsibilities, which may increase the risk of work-related stress and burnout. Workplace-based mind-body activities, including yoga, may support emotional regulation, physical recovery, stress management, and professional well-being.

Using a prospective pre-post observational design, participants will undergo a multidimensional psychological assessment before starting the workplace yoga program and after completing the 10-week program. The evaluation will include measures of burnout, coping strategies, depressive symptoms, anxiety, and satisfaction with the program.

The findings are expected to improve understanding of the potential association between participation in workplace yoga activities and changes in psychological and occupational well-being among healthcare workers. The results may also provide useful information for the development of organizational initiatives aimed at promoting employee well-being and preventing burnout in healthcare settings.

Read the detailed description

This is an observational, prospective, single-arm pre-post study designed to evaluate changes in burnout, stress-related coping strategies, anxiety, depression, and perceived well-being among healthcare workers participating in an existing workplace yoga program.

The study will be conducted at the IRCCS Centro Neurolesi "Bonino-Pulejo", P.O. "Piemonte", Messina, Italy. The yoga program is an organizational well-being initiative already implemented by the institution and is independent of the present research study. The investigators will not organize, deliver, or modify the yoga sessions and will limit their activities to the collection and analysis of observational data.

The study population will consist of adult healthcare professionals, including physicians, nurses, physiotherapists, and healthcare support workers, who voluntarily participate in the workplace yoga program. Participants must be at least 18 years old and be available to attend at least 70% of the scheduled sessions. Individuals with conditions that contraindicate participation in yoga, according to the institutional procedures governing the program, will not be included.

The workplace yoga program consists of 10 sessions conducted outside working hours. Each session lasts up to 60 minutes and includes three phases: an initial warm-up, a central phase involving yoga postures and breathing techniques, and a final phase involving meditation and relaxation. Sessions are conducted by certified instructors and scheduled according to staff shifts to facilitate access.

Participants will undergo assessment at baseline, before the beginning of the program (T0), and at the end of the 10-week program (T1). The multidimensional assessment includes the Copenhagen Burnout Inventory to evaluate personal, work-related, and patient-related burnout; the Brief Coping Orientation to Problems Experienced to assess coping strategies; the Beck Depression Inventory to measure depressive symptoms; and the State-Trait Anxiety Inventory Form Y to assess state and trait anxiety. At follow-up, participants will also complete an ad hoc satisfaction questionnaire rated on a scale from 0 to 10.

The primary objective is to evaluate the change in burnout levels between baseline and follow-up, measured through the Copenhagen Burnout Inventory total score and its subscales.

Secondary objectives include evaluating changes in coping strategies, depressive symptoms, state anxiety, and trait anxiety. Participant satisfaction with the workplace yoga program will also be described. Exploratory analyses may examine whether changes in psychological outcomes differ according to professional role, workplace site, or level of attendance and whether satisfaction is associated with changes in burnout and psychological well-being.

The study does not involve the collection of clinical data, modification of participants' usual healthcare, or the administration of an experimental intervention. Its prospective observational approach aims to describe psychological and occupational changes associated with voluntary participation in an existing organizational yoga program.

The results may contribute to the development of sustainable workplace well-being initiatives aimed at supporting healthcare professionals, reducing burnout risk, and promoting healthier organizational environments.

02

Conditions studied

  • Burnout
  • Occupational Burnout
  • Yoga Therapy

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Keywords

  • healthcare workers
  • burnout
  • coping strategies
  • Psychological Well-Being
  • Organizational Well-Being
03

In context

Burnout, Professional Reclassified

216 studies on the registry are indexed under Burnout, Professional; 33 are open to participants now.

This study's planned enrollment of 70 is below the median of 223 across 52 observational studies indexed under Burnout, Professional.

Browse Burnout, Professional studies →

Lead sponsor

IRCCS Centro Neurolesi Bonino Pulejo is the lead sponsor of 67 studies on the registry; 31 are open to participants now.

Compared within Burnout, Professional, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Burnout, Psychological. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The sample size was determined on the basis of a prior calculation carried out using the G*Power software for a pre-post within-subject comparison (t-test for paired data, two-tailed). Assuming a moderate expected effect on the change in burnout scores (Cohen's d = 0.5), a significance level of α = 0.05 and a statistical power (1-β) of 0.95, the required number of participants is 54 subjects with complete measurements at T0 and T1. However, taking into account the possibility of drop-outs, absences exceeding 30% of the sessions or failure to complete the questionnaires at the follow-up, a loss rate of between 15% and 20% is assumed. Based on this estimate, it is therefore anticipated that a total of approximately 65-70 healthcare professionals will be recruited.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Healthcare professionals, including physicians, nurses, physiotherapists, and healthcare support workers.
  • Age 18 years or older.
  • Voluntary participation in the workplace yoga program.
  • Availability to attend at least 70% of the scheduled yoga sessions.
  • Ability to understand the study procedures and provide written .

Exclusion criteria

Exclusion Criteria:

  • Medical or physical conditions contraindicating participation in yoga, according to the institutional procedures governing the workplace program.
  • Inability to provide .
  • Expected attendance at fewer than 70% of the scheduled sessions.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
70 participants (estimated)
Patient registry
No

Groups and cohorts

  • Healthcare workers

    Burnout

    Behavioral: psychological assessment

Interventions

  • Behavioralpsychological assessment

    Standardized and ad hoc test battery for comprehensive psychological assessment

06

What researchers measure

Primary outcomes

  1. Psychological assessment

    Change in Burnout Levels Copenhagen Burnout Inventory (CBI)

    Time frame: Baseline and 10 weeks

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 26, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07786584
Lead sponsor
IRCCS Centro Neurolesi Bonino Pulejo
Responsible party
Francesco Corallo (Head psychologist, IRCCS Centro Neurolesi Bonino Pulejo) — Principal investigator
First posted
Aug 26, 2026
Start date
May 20, 2026
Primary completion
Dec 20, 2027 (estimated)
Completion
Dec 20, 2027 (estimated)
Last update
Aug 26, 2026

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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