Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT05956756

Resilience Programming for Occupational Therapy Students

Led by Loma Linda University · Updated on 2026-02-06

130

Participants Needed

1

Research Sites

329 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The purpose of this study is to explore the effectiveness of integrated health and resiliency programs into the Entry-Level Doctor of Occupational therapy curriculum. The objectives are to: 1. Determine if students perceive health and resiliency programming as beneficial for their health and well-being 2. Determine if students' lifestyle behaviors, self-esteem, attachment security, and mindfulness improve with health and resiliency programming 3. Determine if students' symptoms of depression and anxiety reduce after participating in health and resiliency programs Students will engage in resilience programming as part of their regular coursework and be invited to complete pre and post assessments to test the effectiveness of programming.

CONDITIONS

Official Title

Resilience Programming for Occupational Therapy Students

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Students enrolled in the Entry Level Doctor of Occupational Therapy program at Loma Linda University
  • Enrollment between June 2023 and June 2029
  • Aged between 18 and 65 years
  • Any gender
  • Any ethnic background
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

AI-Screening

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Trial Site Locations

Total: 1 location

1

Loma Linda Universtiy

Loma Linda, California, United States, 92350

Actively Recruiting

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Research Team

D

Dragana Krpalek, PhD

CONTACT

H

Heather Javaherian, OTD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

PREVENTION

Number of Arms

1

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