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Somatic Psychoeducation for Workplace Stress

N/A

Recruiting

Led By Lourdes P Dale, PhD

Research Sponsored by University of Florida

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up baseline up to 1-month (post-intervention)

Awards & highlights

Study Summary

This trial is exploring ways to improve health & wellness in healthcare providers through a Somatic Psychoeducational Intervention. Researchers will compare pre- & post-intervention assessments to measure effectiveness.

Who is the study for?

This trial is for bedside nurses at least 18 years old working at the University of Florida Health's 8th Street location. It aims to help them with job stress by teaching coping skills and mindfulness through a Somatic Psychoeducational Intervention.Check my eligibility

What is being tested?

The study tests if this intervention can improve emotional, physical, and work health in healthcare providers. Participants will attend classes, complete online assessments, and provide saliva samples before and after the intervention to measure its effects.See study design

What are the potential side effects?

Since this is a psychoeducational intervention focusing on mindfulness and coping strategies rather than medication or medical procedures, significant side effects are not anticipated.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ baseline up to 1-month (post-intervention)

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~baseline up to 1-month (post-intervention)

This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline up to 1-month (post-intervention) for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Measuring Change in Depressive Symptoms using the Patient Health Questionnaire (PHQ-8) self-report questionnaire.

Trial Design

2Treatment groups

Experimental Treatment

Active Control

Group I: Group B: Breath + Movement + PsychoeducationExperimental Treatment1 Intervention

Participants will be asked to participate in the 3 1.5-hour intervention classes. The pre-intervention and post-intervention assessments will require participants to complete a 20-25-minute online survey via Qualtrics and provide saliva samples.

Group II: Group A: Breath + PsychoeducationActive Control1 Intervention

Do I qualify?Apply below to find out

Find a Location

Who is running the clinical trial?

University of FloridaLead Sponsor

1,340 Previous Clinical Trials

715,587 Total Patients Enrolled

Lourdes P Dale, PhDPrincipal InvestigatorUniversity of Florida

Media Library

Somatic Psychoeducational Intervention Clinical Trial Eligibility Overview. Trial Name: NCT05766852 — N/A

Workplace Stress Research Study Groups: Group B: Breath + Movement + Psychoeducation, Group A: Breath + Psychoeducation

Workplace Stress Clinical Trial 2023: Somatic Psychoeducational Intervention Highlights & Side Effects. Trial Name: NCT05766852 — N/A

Somatic Psychoeducational Intervention 2023 Treatment Timeline for Medical Study. Trial Name: NCT05766852 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there any vacancies left to join this clinical trial?

"Data found on the clinicaltrials.gov page confirms that this medical study, which was originally posted on May 22nd 2023 is actively recruiting patients. The trial has since been modified as of May 8th 2023."

Answered by AI

How many people are participating in this clinical investigation?

"Affirmative, according to clinicaltrials.gov records this experiment is currently enrolling individuals. It was initially posted on May 22nd 2023 and most recently updated on the 8th of May in the same year. The research team requires 70 participants from one trial centre only."

Answered by AI

Recent research and studies

AssessmentJournal

Construct Validity of the Five Facet Mindfulness Questionnaire in Meditating and Nonmeditating Samples

Baer, Ruth A., Gregory T. Smith, Emily Lykins, Daniel Button, Jennifer Krietemeyer, Shannon Sauer, Erin Walsh, Danielle Duggan, and J. Mark G. Williams. 2008. “Construct Validity of the Five Facet Mindfulness Questionnaire in Meditating and Nonmeditating Samples”. Assessment. SAGE Publications. doi:10.1177/1073191107313003.

JAMA PsychiatryJournal

Association of Predeployment Heart Rate Variability with Risk of Postdeployment Posttraumatic Stress Disorder in Active-duty Marines

Minassian, Arpi, Adam X. Maihofer, Dewleen G. Baker, Caroline M. Nievergelt, Mark A. Geyer, and Victoria B. Risbrough. 2015. “Association of Predeployment Heart Rate Variability with Risk of Postdeployment Posttraumatic Stress Disorder in Active-duty Marines”. JAMA Psychiatry. American Medical Association (AMA). doi:10.1001/jamapsychiatry.2015.0922.

Academic PsychiatryJournal

A Brief Instrument to Assess Both Burnout and Professional Fulfillment in Physicians: Reliability and Validity, Including Correlation with Self-reported Medical Errors, in a Sample of Resident and Practicing Physicians

Trockel, Mickey, Bryan Bohman, Emi Lesure, Maryam S. Hamidi, Dana Welle, Laura Roberts, and Tait Shanafelt. 2017. “A Brief Instrument to Assess Both Burnout and Professional Fulfillment in Physicians: Reliability and Validity, Including Correlation with Self-reported Medical Errors, in a Sample of Resident and Practicing Physicians”. Academic Psychiatry. Springer Science and Business Media LLC. doi:10.1007/s40596-017-0849-3.

clinicaltrials.govStudy