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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06123507
Other study ID # E2018:008
Secondary ID 48798322464
Status Completed
Phase N/A
First received
Last updated
Start date February 19, 2018
Est. completion date December 20, 2019

Study information

Verified date October 2023
Source University of Manitoba
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This mixed-methods parallel two-arm trial assessed the feasibility, appropriateness, and acceptability of a theoretically-informed intervention designed to improve perspective-taking skills in preparation for a future definitive randomized control trial. Using a 1:1 allocation ratio, student participants (N = 163) in Respiratory, Physical, and Occupational Therapy; Nurse Practitioner; and Kinesiology programs at a Canadian university were randomly assigned to full or partial intervention conditions. Full intervention participants completed an online workshop on perspective-taking and practiced perspective-taking prior to an in-lab 10-minute dialogue with a trained client-actor (masked to condition) about the actor's physical inactivity. Partial intervention participants received the workshop after the dialogue, and were instructed to be aware and mindful of the approach that they took to seek understanding. To be considered feasible, outcomes needed to meet or surpass our criteria (e.g., within-course recruitment: 85-95% of a course when embedded within a course, 5-10% when not embedded). Feasibility and appropriateness were assessed by comparing recruitment rates, protocol, and psychometric outcomes to criteria. Acceptability was assessed by analyzing exit interviews. Recruitment rates, protocol, and psychometric outcomes largely met criteria, and the study was acceptable.


Recruitment information / eligibility

Status Completed
Enrollment 163
Est. completion date December 20, 2019
Est. primary completion date December 20, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Must be a student at the University of Manitoba - Must have completed course content on behaviour change communication Exclusion Criteria: - Full intervention participants were excluded from descriptive statistics calculations if they partially completed the workshop or did not complete all phases due to client-actor availability - Data from participating in additional study sessions were excluded

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Student practitioner perspective-taking intervention
This intervention compares the outcomes where some learn about and practice perspective-taking and others do not. All participants received at least a partial intervention through getting video-feedback on their dialogue with a client actor.

Locations

Country Name City State
Canada University of Manitoba Winnipeg Manitoba

Sponsors (1)

Lead Sponsor Collaborator
University of Manitoba

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Recruitment rate when embedded within a course 85-95% recruitment rate Within 2 years of study commencement (February 2018 - December 2019)
Primary Recruitment rate when not embedded within a course 5-10% recruitment rate Within 2 years of study commencement (February 2018 - December 2019)
Primary Recruitment time Time to finish recruiting in years Within 2 years of study commencement (February 2018 - December 2019)
Primary Program recruitment Count of number of participants per program Within 2 years of study commencement (February 2018 - December 2019)
Primary Workshop completion Percent that completed all pages of the workshop Prior to in-lab participation
Primary Practice time length Time in weeks Prior to in-lab participation
Primary Adherence for not making a plan of action with the client-actor Percent that adhered to instructions Through in-lab completion, an expected average of 2 hours
Primary Lab session length Average lab session length, and time participants spent in the lab in hours and minutes Through in-lab completion, an expected average of 2 hours
Primary Employee training Time in hours Through study completion, up to 2 years
Primary Appropriateness of measure means as assessed by examining data for floor and ceiling effects A scale mean will be created for all measures. To assess appropriateness for inclusion in the definitive trial, we will examine the means for floor and ceiling effects. There should be no evidence of floor or ceiling effects in study measures. If there is evidence of extreme means, then we will consider a different measure for the definitive trial. Post study completion, after 2 years
Primary Amount of missing data To assess appropriateness for inclusion in the definitive trial, the amount of missing data will be examined for each measure. There should be no more than 5% for each study measure. If there is evidence of excessive missing data for a measure, then we will consider a different measure for the definitive trial. Post study completion, after 2 years
Primary Appropriateness of Cronbach's alpha as assessed by an alpha above .70 for each measure To assess appropriateness for inclusion in the definitive trial, we will calculate Cronbach's alpha for each measure. Cronbach's alpha should be at least .70 for each study measure. If there is evidence of low Cronbach's alpha for a measure, then we will consider a different measure for the definitive trial. Post study completion, after 2 years
Secondary Instructor interest Count of instructors who express interest in the study At time of contact through study completion, up to 2 years
Secondary Integration rate Count of how many instructors embedded the course into their study Prior to the study period
Secondary Participant demographics Counts and percentages At baseline
Secondary Prior communication training Counts and percentages for self-reported training At baseline
Secondary Acceptability Examining exit interviews and field notes using manifest content analysis and constant comparison techniques Post study completion, after 2 years
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