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Occupational Distress in Doctors: The Effect of an Induction Programme

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02838290
Enrollment
232
Registered
2016-07-20
Start date
2016-07-31
Completion date
2016-11-30
Last updated
2017-01-31

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Burnout, Professional, Anxiety, Grief, Adaptation, Psychological, Eating Behavior, Alcohol Drinking, Drug Use

Keywords

Burnout, Psychiatric morbidity, Anxiety, Grief, Alcohol and drug use

Brief summary

Background: Over 39% of approximately 3,000 doctors (The British Medical Association quarterly survey, 2015) admitted to frequently feeling drained, exhausted, overloaded, tired, low and lacking energy. Such occupational distress may link to psychological and physical difficulties in doctors and have negative outcomes for organization and patients. The aim of the current study is to investigate the impact of an induction programme on occupational distress of doctors. Methods/design: Doctors will be invited to take part in an online research. Participants will be randomly assigned to the experimental and control groups. Participants in the experimental groups will complete one of the induction topics (about stress at work). Before and after an induction programme participants will be asked to fill in an online survey about their current occupational distress and organizational well-being. Discussion: The investigators expect that doctors' psychological, physiological and organizational well-being will improve after an induction programme which should serve as a resource for better doctor's own health understanding.

Interventions

Participants will be randomly assigned (computer generated straight away after clicking the link to the research) to one of 4 experimental conditions: stress at work, dealing with a patient's death, managing stress at work or all topics together. Each module includes brief reflection parts and quizzes. Participants will be asked to fill in an online survey just before the induction and a week after. The survey is about current occupational distress and organizational factors.

OTHERControl group

Participants in the control group will be asked to fill in an online survey, but will not have any task at time-1. However, participants in the control group will be invited to complete induction programme after time-2 (a week time after time-1) in ensure the same expectations in both, experimental and control, groups.

Sponsors

Birkbeck, University of London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Medical doctors across all specialties and professional grades who have a regular contact with patients and works in the United Kingdom.

Design outcomes

Primary

MeasureTime frameDescription
Drug useA week
The Binge Eating ScaleA week
The Burnout InventoryA week
Alcohol useA week
The Anxiety Disorder ScaleA week
The Grief InventoryA week
The Coping Mechanisms ScaleA weekSelf-distraction, active coping, substance use, use of emotional support, use of instrumental support, positive reframing, humour, self-blame
The Psychiatric Morbidity ScaleA week
The Physical Symptoms ScaleA week
The Insomnia ScaleA week

Secondary

MeasureTime frame
The Work Engagement ScaleA week
The Work-Family Conflict ScaleA week
The Effort-Reward ScaleA week

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 3, 2026