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COMPLETED NA

MBSR Programs to Reduce Compassion Fatigue in Nurses

NCT06436469 · View on ClinicalTrials.gov ↗

Study Summary

The goal of this observational study is to evaluate the effectiveness of a mindfulness-based stress reduction (MBSR) program in reducing compassion fatigue among nurses. The main question it aims to answer is: Does participation in an MBSR program decrease levels of compassion fatigue among nurses? The primary hypothesis is that nurses who participate in the MBSR program will experience a significant reduction in compassion fatigue after implementing the interventions. Participants will include psychiatric nurse practitioners working in high-stress environments. Participants will: Attend a series of MBSR sessions over a specified period. Engage in mindfulness practices such as body scans, and deep breathing. Complete self-report measures to assess levels of compassion fatigue before and after the intervention.

Conditions Studied

Interventions

  • BEHAVIORAL Mindfulness-Based Stress Reduction (MBSR) Program

Study Locations (1)

Florida

  • My Psychiatrist — Hollywood

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2024-07-01
Est. Completion 2024-08-11
Phase NA

Sponsor

Nova Southeastern University

82 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06436469

The ClinicalTrials.gov registry entry for NCT06436469 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Nova Southeastern University, which has 82 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Compassion Fatigue appearing as the primary indexed condition, and to 1 intervention — of which Mindfulness-Based Stress Reduction (MBSR) Program is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06436469 reports 1 study location spanning 1 distinct geographic area — top geographies include Florida. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT06436469 about?

NCT06436469 is a clinical study titled "MBSR Programs to Reduce Compassion Fatigue in Nurses". The goal of this observational study is to evaluate the effectiveness of a mindfulness-based stress reduction (MBSR) program in reducing compassion fatigue among nurses. The main question it aims to answer is: Does participation in an MBSR program decrease levels of compassion fatigue among nurses?...

What is the current status of trial NCT06436469?

This trial is currently completed. It is a NA study. The enrollment target is 11 participants. The study started on 2024-07-01. Estimated completion is 2024-08-11.

What conditions does trial NCT06436469 study?

This clinical trial studies the following conditions: Compassion Fatigue. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06436469?

The interventions under investigation include: Mindfulness-Based Stress Reduction (MBSR) Program (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06436469?

This trial is sponsored by Nova Southeastern University, which has 82 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06436469 being conducted?

This trial has 1 study location across Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial