Using IF-THEN Plans to Support Healthcare Professionals in Raising Patient Safety Concerns

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Manchester

About this trial

This study aims to test whether a brief behavioural intervention can help healthcare professionals raise and respond to patient safety concerns in their work. Healthcare professionals are often encouraged to speak up about safety risks, but barriers such as time pressure, uncertainty, and workplace culture can make this difficult.

Participants will complete an online questionnaire about their experiences of patient safety risks and how often they raise concerns. They will then be randomly assigned to one of two groups. One group will complete a short planning exercise ("if-then" plans) designed to help them act when they notice safety concerns, while the other group will not receive this exercise. Participants will be invited to complete follow-up questionnaires at approximately one month and six months to assess how often they have raised or responded to safety concerns since taking part.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Currently working as a healthcare professional in a health or social care setting

Good understanding of written and spoken English

Disqualifiers

Aged under 18 years

Not currently working as a healthcare professional in a health or social care setting

Poor understanding of written and spoken English

Trial design

Design model

Parallel

Treatments tested in this trial

  • Implementation intention planning

    Behavioral

    Implementation intention planning to promote patient safety concerns

Treatment groups

1,000 Participants
are divided into 2 treatment groups
Group A: Intervention (volitional help sheet)Experimental treatment 1 intervention
Group B: ControlNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Raising safety concerns

Self-reported frequency of raising and responding to patient safety concerns at 1-month and 6-month follow-up.

Time frame
1 month, 6 months.

Secondary outcomes

1

Capability, opportunity and motivation (based on the COM-B model) measured at baseline, 1-month, and 6-month follow-up.

Measured using the Capability, Opportunity, Motivation questionnaire. Each of the items (0-10 scale) will be analysed separately as these each measure a separate construct. Higher scores indicate higher agreement with statements.

Time frame
1 month, 6 months.

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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University of Manchester

Lead sponsor

University of Leeds

Collaborator

This trial is not recruiting at the moment. You can still explore other options: