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A Pragmatic Feasibility Trial to Promote Student Perspective-Taking on Client Physical Activity: A Collaborative Project

Not Applicable
Completed
Conditions
Communication
Interventions
Behavioral: Student practitioner perspective-taking intervention
Registration Number
NCT06123507
Lead Sponsor
University of Manitoba
Brief 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
163
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

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Partial intervention conditionStudent practitioner perspective-taking interventionThe Partial intervention condition involved video-feedback alone. In this condition, participants were provided with a link to the perspective-taking workshop after the study was complete.
Full educational intervention conditionStudent practitioner perspective-taking interventionThe Full intervention condition included a perspective-taking workshop plus independent practice and video-feedback
Primary Outcome Measures
NameTimeMethod
Adherence for not making a plan of action with the client-actorThrough in-lab completion, an expected average of 2 hours

Percent that adhered to instructions

Amount of missing dataPost study completion, after 2 years

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.

Appropriateness of Cronbach's alpha as assessed by an alpha above .70 for each measurePost study completion, after 2 years

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.

Practice time lengthPrior to in-lab participation

Time in weeks

Program recruitmentWithin 2 years of study commencement (February 2018 - December 2019)

Count of number of participants per program

Appropriateness of measure means as assessed by examining data for floor and ceiling effectsPost study completion, after 2 years

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.

Lab session lengthThrough in-lab completion, an expected average of 2 hours

Average lab session length, and time participants spent in the lab in hours and minutes

Recruitment rate when embedded within a courseWithin 2 years of study commencement (February 2018 - December 2019)

85-95% recruitment rate

Recruitment rate when not embedded within a courseWithin 2 years of study commencement (February 2018 - December 2019)

5-10% recruitment rate

Recruitment timeWithin 2 years of study commencement (February 2018 - December 2019)

Time to finish recruiting in years

Workshop completionPrior to in-lab participation

Percent that completed all pages of the workshop

Employee trainingThrough study completion, up to 2 years

Time in hours

Secondary Outcome Measures
NameTimeMethod
Instructor interestAt time of contact through study completion, up to 2 years

Count of instructors who express interest in the study

Integration ratePrior to the study period

Count of how many instructors embedded the course into their study

Participant demographicsAt baseline

Counts and percentages

Prior communication trainingAt baseline

Counts and percentages for self-reported training

AcceptabilityPost study completion, after 2 years

Examining exit interviews and field notes using manifest content analysis and constant comparison techniques

Trial Locations

Locations (1)

University of Manitoba

🇨🇦

Winnipeg, Manitoba, Canada

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