NCT01512823

Brief Summary

This pragmatic randomised controlled trial (RCT) used a two-group parallel design with matched-pair stratification by type (clinician/manager) and knowledge score. The trial aimed to: 1) determine whether an IE was more effective than a DE for improving EBP knowledge, skills and use at 12 weeks, and 2) to investigate the feasibility of conducting a RCT with occupational therapists in a public health setting. Occupational therapists employed by the Western Cape Department of Health (DOH) form,ed the study population(N=98). Fifty-eight consented to participate and were randomly allocated to either an interactive (IE) or a didactic (DE) educational intervention using coin tossing. Data was collected at baseline and 12 weeks The primary outcome was increased EBP knowledge at 12 weeks shown by an improved total knowledge score. Secondary outcomes were improved attitudes and behaviour. Data were collected at the health facilities where participants were employed. Raters for the audit were blinded but participants and the provider could not be blinded. Thirty participants were allocated to receive the IE and 28 the DE. Twenty-five participants in the IE and 21 in the DE completed the trial and were included in the 12 week analysis. Results revealed no significant difference between the groups in the primary knowledge outcome at 12 weeks. Examination of within-group changes revealed significant improvements in knowledge in both groups (IE: T=4.0, p\<0.001; DE: T=12.0, p=0.002), but the IE also showed a significant increase in behaviour (T=64.5, p=0.044) and attitudes on one sub-scale (T=33.0, p=0.039). As the study was powered at 43%, it may have failed to detect significant differences at 12 weeks. Conducting a high-quality RCT was feasible and the risk of bias was assessed as low. The OTEBP trial adds strength to the existing evidence that both didactic and interactive educational interventions can improve knowledge, but it seems that interactive interventions may be more effective for changing behaviour. High-quality pragmatic trials can feasibly be conducted within the public health service

Trial Health

87
On Track

Trial Health Score

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

Enrollment
58

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Nov 2007

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

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

Study Start

First participant enrolled

November 1, 2007

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 1, 2009

Completed
2.2 years until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2011

Completed
11 months until next milestone

First Submitted

Initial submission to the registry

January 13, 2012

Completed
6 days until next milestone

First Posted

Study publicly available on registry

January 19, 2012

Completed
Last Updated

February 6, 2012

Status Verified

February 1, 2012

Enrollment Period

1.2 years

First QC Date

January 13, 2012

Last Update Submit

February 3, 2012

Conditions

Keywords

randomised controlled trialeducational interventionoccupational therapy

Outcome Measures

Primary Outcomes (1)

  • Shortened Fresno Test of Competence in Evidence-based Practice (SAFT)

    Modified from the Adapted Fresno Test of Competence in EBP (AFT) (McCluskey and Bishop, 2009), the SAFT consists of three items testing knowledge of writing a PICO question based on a clinical scenario, ability to identify the most suitable study design to answer the question, and knowledge of possible sources of information. The total possible score is 30 points. The test is scored using a grading rubric. Two versions are availbale for measuring outcomes of educational interventions.

    12 weeks

Secondary Outcomes (1)

  • Audit checklist

    12 weeks

Study Arms (2)

Interactive educational intervention

EXPERIMENTAL

Two education sessions (four-hours and two-hours respectively), emailed notes and reminders

Behavioral: Education

Didactic educational intervention

EXPERIMENTAL

Education alone

Behavioral: Education

Interventions

EducationBEHAVIORAL

Interactive educational intervention: * 4 hour education session (with notes and 'evidence packs'); presentations, small group discussion tasks and practice of particular skills - 2 hour session (1 week later) * Emailed notes from second session * Telephonic/email follow-up (reminders) Didactic educational intervention: \- 4 hour education session (with notes and 'evidence packs'; questions answered but no discussion or application of skills

Didactic educational interventionInteractive educational intervention

Eligibility Criteria

Age21 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Occupational therapists employed by the Western Cape Department of Health (DOH)
  • Working at least 20 hours per week

You may not qualify if:

  • Working at a distance of more than 1½ hours from Cape Town
  • Therapists who would be leaving the DOH before December 2008 or taking leave during the time of the intervention

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Cape Town

Cape Town, Western Cape, 7925, South Africa

Location

Related Publications (2)

  • Buchanan H, Jelsma J, Siegfried N. Measuring evidence-based practice knowledge and skills in occupational therapy--a brief instrument. BMC Med Educ. 2015 Oct 30;15:191. doi: 10.1186/s12909-015-0475-2.

  • Buchanan H, Siegfried N, Jelsma J, Lombard C. Comparison of an interactive with a didactic educational intervention for improving the evidence-based practice knowledge of occupational therapists in the public health sector in South Africa: a randomised controlled trial. Trials. 2014 Jun 10;15:216. doi: 10.1186/1745-6215-15-216.

MeSH Terms

Conditions

Behavior

Interventions

Educational Status

Intervention Hierarchy (Ancestors)

Socioeconomic FactorsPopulation Characteristics

Study Officials

  • Helen Buchanan, PhD

    University of Cape Town

    PRINCIPAL INVESTIGATOR
  • Nandi Siegfried, PhD

    South African Cochrane Centre & University of Cape Town

    STUDY DIRECTOR
  • Jennifer Jelsma, PhD

    University of Cape Town

    STUDY DIRECTOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal investigator

Study Record Dates

First Submitted

January 13, 2012

First Posted

January 19, 2012

Study Start

November 1, 2007

Primary Completion

January 1, 2009

Study Completion

March 1, 2011

Last Updated

February 6, 2012

Record last verified: 2012-02

Locations