Integrating NIH Reset Stress Strategies Into DPT Curriculum

January 13, 2023 updated by: Shannon Dudash, Youngstown State University

The goal of this longitudinal prospective cohort study is to determine effectiveness of integrating NIH reset stress strategies of deep breathing, muscle relaxation and mindfulness in DPT students in order to help them reduce stress throughout their schooling.

The main question[s] it aims to answer are:

  • Do performing the NIH reset stress strategies help DPT students manage their stress
  • Do DPT students find these strategies helpful Participants will be asked to fill out initial intake forms and participate in weekly sessions of five to ten minutes that will be either a deep breathing, mindfulness, or muscle relaxation activity led by faculty member. DPT students will then rate their stress level weekly on a numeric stress scale.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Integrating NIH Reset Stress Strategies into DPT Curriculum A. Investigator Information

  1. Primary Investigator: Shannon Dudash PT, DPT, GCS
  2. Co-Investigators: Weiqing Ge PhD, PT, Nancy Landgraff PhD, PT, Cara Berg-Carramusa EdD, PT B. Sponsor/Funding Information

a. Not applicable C. Location of Research

a. Youngstown State University D. Conflict of Interest

a. none E. Methods and Procedures

a. Introduction i. DPT students report higher levels of stress and anxiety compared to their age matched peers (1). Since 2020, COVID has caused increased stress among students and the general population (11, 12). Increased stress can negatively impact not only students' physical conditions but also their academic performance. This may potentially have long term consequences that carry over into their careers and lead to decreased quality of future healthcare workers. There is a lack of information on if and how DPT programs address stress in DPT students in their curriculum. Deep breathing, muscle relaxation and mindfulness are strategies recommended by the NIH to help manage stress to general public which can potentially be used by DPT program to help DPT students manage their stress and be successful. However, there is lack of evidence on the use of these strategies to assist DPT students manage stress and anxiety during their schooling.

b. Background i. Long term stress, or chronic stress, can lead to serious health problems including disrupted sleep, muscle tension, metabolic dysfunction, immune abnormalities, and inflammation. Some diseases such as cardiovascular disease, diabetes, cancer, autoimmune diseases, depression, and anxiety orders can be linked to chronic stress.

ii. Deep breathing, mindfulness, and muscle relaxation have been used to manage stress in older and younger adult populations (3, 4, 6, 13).

c. Objectives i. The purpose of this study is to determine the effectiveness of integrating NIH reset stress strategies of deep breathing, muscle relaxation and mindfulness for DPT students in order to help them reduce stress throughout their schooling.

d. Study design and procedures i. How the participants will be identified and recruited and how informed consent will be obtained to minimize coercion or undue influence: The study design is a longitudinal prospective cohort study. Students in the Doctor of Physical Therapy program will be recruited by email about the "Integrating NIH Reset Stress Strategies into DPT Curriculum" project, NIH Reset Stress flyer, and an informed consent form from the student worker in the Graduate of Health Sciences department. A recruitment flyer will be posted within the department. Also, a current student will recruit within the DPT classes. If students choose to participate, they will turn in their signed informed consent to Shannon Dudash by the end of week 1 of the spring semester.

ii. Procedures for data collection: Initial meeting will be established with participants to fill out intake paperwork including survey asking if participants know what deep breathing, muscle relaxation, and mindfulness are, demographic information, DASS-21, PSS-10 and Stress Numeric Scale.

iii. Procedures to which human subjects will be exposed: Reset Stress sessions will be administered prior to the start of a weekly class by the course instructor (Shannon Dudash). The focus of the sessions will be a combination of mindfulness, deep breathing, and muscle relaxation. These sessions will last approximately 5-10 minutes. Sessions will be performed in a group setting. There will be a total of 12-14 sessions administered throughout the 2023 Spring semester at YSU on a weekly basis.

iv. Procedures for data collection: Participants will fill out a Stress Numeric Scale after each weekly intervention session. Participants will also be asked to complete the DASS-21, Stress Numeric Scale, and PSS-10 at a midpoint check-in during week 6 and at the end of the project. An additional survey at the end of the project inquiring if it was helpful to learn these stress management strategies and how frequently participants used them independently will be administered.

v. Any paper forms used will not have any identification on them to protect participant privacy. Anonymous Slido presentation will be used to collect weekly Stress Numeric scale ratings.

vi. Data Analysis will include comparison of surveys from start to completion of sessions. We will use a repeated measure ANOVA to look at trends of Stress Numeric scale over the spring semester. Descriptive analysis will also include participants' responses on how frequently they used the stress management strategies independently and if they found that the strategies taught were beneficial.

e. No deception is to be used in this study. f. Participants will not be presented with materials that they might regard to be offensive, threatening or degrading.

F. Risk/Benefit Assessment a. Potential risks: It is unlikely, but the participants might have negative feelings by recalling previous experience when completing the questionaries. It will be no more than what they feel in normal daily life.

G. Potential benefits: Benefits from this study include learning different strategies to control stress. Implementing the strategies may reduce stress, improve physical conditions, and improve academic performance.

H. Human Research Participants

a. Students enrolled in Doctor of Physical Therapy program at Youngstown State University i. Inclusion criteria: age > 18 years old, enrolled in DPT program ay YSU, ability to follow instructions to perform deep breathing, muscle relaxation, and mindfulness strategies.

ii. Exclusion criteria: age < 18 years old, not enrolled in DPT program at YSU I. Recruitment Procedures

  1. Students in the Doctor of Physical Therapy program will be recruited by email about the "Integrating NIH Reset Stress Strategies into DPT Curriculum" project, NIH Reset Stress flyer and an informed consent form from the student worker in the Graduate of Health Sciences department. A recruitment flyer will be posted within the department. Also, a current student will recruit within the DPT classes.
  2. If students choose to participate, they will turn in their signed informed consent to Shannon Dudash by the end of week 1 of the spring semester.

J. Informed Consent and Assent

  1. Informed consent attached to IRB application separately
  2. No minors, prisoners, or individuals with intellectual disabilities will be included in this study.
  3. The record of informed consent will be stored in the principal investigator's office in a locked filing cabinet.

K. Confidentiality of Information Collected

  1. All outcome measures will be collected anonymously. No names of the participants will be collected except the informed consent form.
  2. Data will be stored on Research laptop computer that is password protected. All signed informed consent forms will be stored in a locked file cabinet in a locked office on Youngstown State University Campus and will be shredded after 3 years in accordance with IRB standards.

Study Type

Interventional

Enrollment (Anticipated)

80

Phase

  • Not Applicable

Contacts and Locations

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

Study Contact

  • Name: Shannon Dudash, DPT
  • Phone Number: 3309412407
  • Email: sstarr@ysu.edu

Study Locations

  • United States
    • Ohio
      • Youngstown, Ohio, United States, 44555-0001
        • Recruiting
        • Youngstown State University
        • Contact:

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

18 years to 40 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • DPT student at Youngstown State University
  • > 18 years old
  • Have the ability to follow instructions to perform deep breathing, muscle relaxation, and mindfulness strategies

Exclusion Criteria:

  • Not a DPT student at Youngstown State University
  • Under 18 years of age

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

  • Primary Purpose: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: DPT students at YSU
Behavioral: deep breathing, muscle relaxation, and mindfulness
5-10-minute group sessions will be administered to DPT students teaching them the NIH recommended strategies of deep breathing, muscle relaxation or mindfulness.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
PSS-10
Time Frame: through study completion, an average of 1 year
Stress questionnaire
through study completion, an average of 1 year
DASS-21
Time Frame: through study completion, an average of 1 year
Depression, stress and Anxiety questionnaire
through study completion, an average of 1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Stress Numeric scale
Time Frame: through study completion, an average of 1 year
1 through 10 scale rating stress level from nothing to extremely high
through study completion, an average of 1 year

Collaborators and Investigators

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

Sponsor

Youngstown State University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

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 (Anticipated)

January 15, 2023

Primary Completion (Anticipated)

January 15, 2024

Study Completion (Anticipated)

January 15, 2024

Study Registration Dates

First Submitted

January 5, 2023

First Submitted That Met QC Criteria

January 13, 2023

First Posted (Estimate)

January 25, 2023

Study Record Updates

Last Update Posted (Estimate)

January 25, 2023

Last Update Submitted That Met QC Criteria

January 13, 2023

Last Verified

January 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 2023-155

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.

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