NCT02838290

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.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
232

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jul 2016

Shorter than P25 for not_applicable

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 6, 2016

Completed
25 days until next milestone

Study Start

First participant enrolled

July 1, 2016

Completed
19 days until next milestone

First Posted

Study publicly available on registry

July 20, 2016

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2016

Completed
Last Updated

January 31, 2017

Status Verified

January 1, 2017

Enrollment Period

4 months

First QC Date

June 6, 2016

Last Update Submit

January 30, 2017

Conditions

Keywords

BurnoutPsychiatric morbidityAnxietyGriefAlcohol and drug use

Outcome Measures

Primary Outcomes (10)

  • The Anxiety Disorder Scale

    A week

  • The Grief Inventory

    A week

  • The Coping Mechanisms Scale

    Self-distraction, active coping, substance use, use of emotional support, use of instrumental support, positive reframing, humour, self-blame

    A week

  • The Psychiatric Morbidity Scale

    A week

  • The Physical Symptoms Scale

    A week

  • The Insomnia Scale

    A week

  • The Binge Eating Scale

    A week

  • The Burnout Inventory

    A week

  • Alcohol use

    A week

  • Drug use

    A week

Secondary Outcomes (3)

  • The Effort-Reward Scale

    A week

  • The Work Engagement Scale

    A week

  • The Work-Family Conflict Scale

    A week

Study Arms (2)

Induction

EXPERIMENTAL
Other: Induction

Control group

OTHER
Other: Control group

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.

Induction

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.

Control group

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (2)

  • Medisauskaite A, Kamau C. Does occupational distress raise the risk of alcohol use, binge-eating, ill health and sleep problems among medical doctors? A UK cross-sectional study. BMJ Open. 2019 May 15;9(5):e027362. doi: 10.1136/bmjopen-2018-027362.

  • Medisauskaite A, Kamau C. Reducing burnout and anxiety among doctors: Randomized controlled trial. Psychiatry Res. 2019 Apr;274:383-390. doi: 10.1016/j.psychres.2019.02.075. Epub 2019 Mar 1.

MeSH Terms

Conditions

Burnout, ProfessionalAnxiety DisordersFeeding BehaviorAlcohol DrinkingBurnout, Psychological

Interventions

Neoadjuvant TherapyControl Groups

Condition Hierarchy (Ancestors)

Occupational StressOccupational DiseasesStress, PsychologicalBehavioral SymptomsBehaviorMental DisordersBehavior, AnimalDrinking Behavior

Intervention Hierarchy (Ancestors)

Combined Modality TherapyTherapeuticsEpidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Doctoral Researcher

Study Record Dates

First Submitted

June 6, 2016

First Posted

July 20, 2016

Study Start

July 1, 2016

Primary Completion

November 1, 2016

Study Completion

November 1, 2016

Last Updated

January 31, 2017

Record last verified: 2017-01

Data Sharing

IPD Sharing
Will not share