Have Physical Therapists Attitudes and Beliefs Towards Vital Assessment Changed Following the COVID-19 Pandemic?

January 22, 2024 updated by: Youngstown State University
Previous studies prior to the COVID-19 pandemic show that cardiovascular and blood pressure assessment by physical therapists is inadequate or lacking despite prior training. Since the COVID-19 pandemic, assessment of cardiovascular and respiratory function may become more critical as the manifestation of long COVID has become a concern. The purpose of this study is to determine whether physical therapists' attitudes and beliefs towards vital sign assessment have changed following the COVID-19 pandemic.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

500

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

Study Locations

    • Ohio
      • Youngstown, Ohio, United States, 44555
        • Recruiting
        • Youngstown State University
        • Contact:
        • Principal Investigator:
          • Edmund C Ickert, PhD

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

Physical Therapists who are currently working in clinical practice that have a minimum of 5 years experience (based on ability to identify practice patterns prior to the COVID-19 pandemic).

Description

Inclusion Criteria:

  1. Must be a licensed Physical Therapist
  2. Must be actively be involved in clinical practice
  3. Must have ≥ 5 years of experience practicing in a clinical setting as a Physical Therapist

Exclusion Criteria:

(1) Did not provide informed consent

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Physical Therapists

Physical Therapists currently working in a clinical setting.

Group Participants (Inclusion/Exclusion Criteria)

Inclusion Criteria:

  1. Must be a licensed Physical Therapist
  2. Must be actively be involved in clinical practice
  3. Must have ≥ 5 years of experience practicing in a clinical setting as a Physical Therapist

Exclusion Criteria:

(1) Did not provide informed consent

The survey will be disseminated across the American Physical Therapy Association (APTA) email lists. Further potential candidates may be identified through existing professional networks, clinical settings, and social medial/internet-based searching.

This is a cross-sectional study that utilizes a KAP (knowledge, attitude, and practice) survey. This type of survey can be conducted on a representative sample of physical therapists who are currently involved in clinical practice. These types of surveys are useful for identifying gaps between what people know and how they act on that knowledge. There have been previous studies that have utilized KAP surveys when identifying knowledge, attitude, and practice behaviors of physical therapists.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
KAP Survey
Time Frame: Baseline

The KAP Survey is divided into multiple sections (4 total) as outlined below:

  1. Demographic: Questions related to sample population (therapist) characteristics
  2. Prior COVID-19: Questions related to therapist attitudes and practices regarding vital assessment prior to COVID-19 pandemic.
  3. After COVID-19: Questions related to therapist attitudes and practices regarding vital assessment following COVID-19 pandemic.
  4. Knowledge: General knowledge questions related to vital assessment.
Baseline

Collaborators and Investigators

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

Collaborators

Investigators

  • Principal Investigator: Edmund C Ickert, PhD, 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.

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)

September 8, 2023

Primary Completion (Estimated)

May 1, 2024

Study Completion (Estimated)

May 1, 2024

Study Registration Dates

First Submitted

June 15, 2023

First Submitted That Met QC Criteria

June 15, 2023

First Posted (Actual)

June 18, 2023

Study Record Updates

Last Update Posted (Estimated)

January 24, 2024

Last Update Submitted That Met QC Criteria

January 22, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

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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