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HealthyNCT06939101

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

An observational study of Healthy, run by Texas Woman's University at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 65 yearsHealthy volunteers can take part
Conditions the study is for
Healthy
What is being tested?
self-efficacy training
How many people
14 participants
Where
1 siteUnited States
Study dates
7 May 2024to 16 Aug 2024
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 65 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

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.

Who may be able to join

  • 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.

Who cannot join

  • Students from other academic institutions.

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Texas Woman's University

    Dallas, Texas, 75235-7200

Other trials in United States

About this study

Official title: 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.

Read the 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.

Conditions
Healthy
Being tested
self-efficacy training
Keywords
interdisciplinary, Collaboration, education, interaction, evaluation and feedback

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • self-efficacy trainingBehavioural

    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 and six 1-2 hours of debriefing after each clinical day.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Self-efficacy intereprofessional experiential scale and six open end questions

    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.

    Measured: pre-post trip surveys about 2 weeks apart

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted22 Apr 2025
  2. Study start7 May 2024
  3. Primary completion16 Aug 2024
  4. Study completion16 Aug 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Cross-sectional
Enrolment
14 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06939101
Sponsor's protocol ID
IRB-FY2024-248
Status last verified
Apr 2025
First submitted
7 Apr 2025
Last updated
23 Apr 2025
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Healthy, run by Texas Woman's University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 23 Apr 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Self-efficacy intereprofessional experiential scale and six open end questions (time frame: pre-post trip surveys about 2 weeks apart). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Apr 2025; AzTrials last refreshed its copy on 26 Oct 2026.

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