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Using IF-THEN Plans to Increase Behaviour Change Intervention Delivery

NCT05820282 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1008

Last updated 2024-12-09

No results posted yet for this study

Summary

The aim of the present research is to test the effectiveness of an implementation intention-based intervention for increasing healthcare professional delivery of behaviour change interventions during routine healthcare.

Each participant will be randomly allocated to one of two conditions. The two conditions are: (1) a control condition, and (2) intervention (form multiple implementation intentions from a drop-down menu). The main outcome measure will be use of face coverings.

Conditions

  • Health Behavior

Interventions

BEHAVIORAL

Volitional help sheet

Participants are asked to choose from a list of strategies for increasing delivery of behaviour change interventions

OTHER

Control condition

Participants are asked to identify situations and solutions and place a tick next to each one they think would be useful to them. Therefore, participants in the control condition are not asked to form implementation intentions.

Sponsors & Collaborators

  • University of Manchester

    collaborator OTHER

  • University of Leeds

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-02-24
Primary Completion
2023-05-31
Completion
2023-05-31

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05820282 on ClinicalTrials.gov