Self-efficacy for Interprofessional Experiential Learning Through an International Service Trip

April 21, 2025 updated by: William Sit, Texas Woman's University

Self-efficacy for Interprofessional Experiential Learning Through an International Service Trip: a Mixed-methods Study

This pilot mixed-methods educational study examines the impact of interprofessional experiential learning on self-efficacy during a service trip to Guatemala. Methods: Fourteen participants were recruited from occupational therapy, physical therapy, and speech pathology students at a university. They engaged in a 9-day international interprofessional learning service trip and completed pre- and post-surveys with open-ended questions to measure and reflect on the impact of service trips on self-efficacy.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Description of the service trip The principal investigator is spearheading an education abroad trip to Guatemala involving TWU doctoral entry-level occupational therapy, doctoral physical therapy, and master speech therapy students, building on the program's participation in 2023. The principal investigator will supervise students and build this program to increase occupational, physical, and speech therapy student participation. There are two one-hour briefing meetings for onboarding to promote self-efficacy preparation. The aim is to enhance occupational, physical, and speech therapy student involvement, with the opportunity for subjects to earn credit for Fieldwork I. Organized in collaboration with Hearts in Motion (HIM), an organization dedicated to providing care in areas of need, the 9-day trip from Friday, May 17 to Sunday, May 26, 2024, focuses on improving subjects' self-efficacy for interprofessional experiential learning by offering therapy services to underserved areas in Guatemala. Guatemala is one of the most populated countries in Latin America, and 59.3% of the population lives in poverty. The HIM organizes where the subjects go each day. Upon arrival at a site, the group will break into groups of 2-3 subjects to see each patient, one at a time. Sometimes the subjects are at one of the established therapy clinics HIM runs; sometimes, the subjects have what are called "pop-up" clinics, which is when the subjects go to a town and provide therapy services in a space HIM provides for the subjects (not a clinic; it's usually a church, school, gym, etc.). Every one of the six clinical days has about 30 minutes of briefing before the clinical trip to promote self-efficacy interaction and 60 minutes of debriefing with the PI after the trip for reflection in interprofessional evaluation and feedback on self-efficacy.

Recruitment will begin with the co-investigator sending an email to all TWU students within the occupational, physical, and speech therapy departments regarding the service trip. Following that message, an email from the principal researcher will be sent to the potential subjects who have committed to participating in the trip (see recruiting email attachment in Section 6: subject recruitment), subjects will complete a pre-trip online survey using Qualtrics, assessing their self-efficacy for interprofessional experiential learning. To facilitate post-trip survey matching, subjects will input four digits, comprising their first name initial, two digits of their birthday (01-31), and the last digit of their phone number. All subjects will partake in the same service trip, and upon their return to the United States, they will repeat the survey to evaluate the impact of experiential learning on their confidence levels. Subsequently, subjects will be invited by the PI via a post-trip email to complete an online post-trip survey, compare their self-efficacy for interprofessional experiential learning post-trip, and respond to six open-ended questions about motivation, knowledge, skills, and satisfaction arising from their learning experiences and reflection. Those who have chosen not to participate will receive the email, but they can only accept it if it is applicable.

Throughout the study, communication will be via email, with no video or audio components, allowing subjects to choose a comfortable and private location for survey completion. The estimated time commitment for subjects is 15 minutes for the pre-trip survey and 25 minutes for the post-trip survey, totaling 40 minutes for the entire study. The qualitative method will yield descriptive data from the six open-ended questions only in the post-trip survey created by the PI on subjects' perceived experiences and self-efficacy growth, while closed-ended survey questions will be quantitatively analyzed using SPSS with a repeated measures ANOVA test. The principal investigator and a research team member will analyze qualitative data from open-ended survey questions using a co-coding method with the PI and research team members for rigor and trustworthiness to enhance interrater reliability. A co-principal investigator will be consulted if a disagreement arises between the PI and two research members to come to a consensus during the data analysis.

Study Type

Observational

Enrollment (Actual)

14

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Texas
      • Dallas, Texas, United States, 75235-7200
        • Texas Woman's University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The potential subjects in this study consist of approximately 25 Texas Woman's University students from the Occupational Therapy (OT), Physical Therapy (PT), and Speech Therapy (ST) departments.

Description

Inclusion Criteria:

  • Must be at least 18 years old. Plan to attend the service trip in Guatemala. Interprofessional students from the School of Physical Therapy, Occupational Therapy, and Speech Pathology.

Students who have treated clients with other professionals on the service trip.

Exclusion Criteria:

  • Students from other academic institutions.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-efficacy intereprofessional experiential scale and six open end questions
Time Frame: pre-post trip surveys about 2 weeks apart
The pre-trip test consists of five demographic questions. A repeated survey consisting of 16 was developed, tested, and administered pre- and post-trip to measure the dependent variables, which is a highly validated and reliable measurement tool created by Mann. et al. . The confidence variables were measured on a ten-choice Likert scale to reduce central tendency bias. Confidence level was assessed through multiple-choice questions formatted to elicit clinical reasoning based on two factors, including interprofessional interaction and interprofessional evaluation and feedback. The six open-ended questions in the post-trip survey were developed by the research team and reviewed by a biostatistician using survey methods.
pre-post trip surveys about 2 weeks apart

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: william sit, PhD, Texas Woman's University (TWU)

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

May 7, 2024

Primary Completion (Actual)

August 16, 2024

Study Completion (Actual)

August 16, 2024

Study Registration Dates

First Submitted

April 7, 2025

First Submitted That Met QC Criteria

April 14, 2025

First Posted (Actual)

April 22, 2025

Study Record Updates

Last Update Posted (Actual)

April 23, 2025

Last Update Submitted That Met QC Criteria

April 21, 2025

Last Verified

April 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • IRB-FY2024-248

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Healthy

Clinical Trials on self-efficacy training

Subscribe