Arm A, Study Period 1 (Mindfulness and Sleep Hygiene): for Compassion Fatigue

Children's National Health System, Washington, United States
Compassion Fatigue+1 More ConditionsMindfulness and Sleep Hygiene - Behavioral
Eligibility
18+
All Sexes

Study Summary

This trial will assess the impact of two interventions on nightshift health care workers' quality of life & errors.

Eligible Conditions
  • Compassion Fatigue

Treatment Effectiveness

Phase-Based Effectiveness

1 of 3
N/A

Similar Trials

1
SLEEP program
1
CBTi with Application
3
Sleep Hygiene Education

Study Objectives

1 Primary · 1 Secondary · Reporting Duration: 60 days before Baseline, Week 8 and Week 16

Week 16
Change in Medication Error Administration
Week 16
Change in the PROMIS Sleep Disturbance Measure
Change in the PROMIS Sleep-Related Impairment Measure (SRI)
change in Role-Related Meaning
Week 16
Professional Quality of Life Scale, (ProQOL-21). The variable will be change in professional quality of life as measured by the Professional Quality of Life Scale, (ProQOL-21).

Trial Safety

Phase-Based Safety

1 of 3

Similar Trials

1
SLEEP program
2
CBTi with Application
3
Sleep Hygiene Education

Awards & Highlights

No Placebo Group
All patients enrolled in this trial will receive the new treatment.

Trial Design

2 Treatment Groups

Arm B, Study Period 1 (Physical Activity and Sleep Hygiene):
1 of 2
Arm A, Study Period 1 (Mindfulness and Sleep Hygiene):
1 of 2

Active Control

Experimental Treatment

221 Total Participants · 2 Treatment Groups

Primary Treatment: Arm A, Study Period 1 (Mindfulness and Sleep Hygiene): · No Placebo Group · N/A

Arm A, Study Period 1 (Mindfulness and Sleep Hygiene):
Behavioral
Experimental Group · 1 Intervention: Mindfulness and Sleep Hygiene · Intervention Types: Behavioral
Arm B, Study Period 1 (Physical Activity and Sleep Hygiene):
Behavioral
ActiveComparator Group · 1 Intervention: Phyical activity and Sleep Hygiene · Intervention Types: Behavioral

Trial Logistics

Trial Timeline

Screening: ~3 weeks
Treatment: Varies
Reporting: 60 days before baseline, week 8 and week 16

Who is running the clinical trial?

Children's National Research InstituteLead Sponsor
195 Previous Clinical Trials
206,257 Total Patients Enrolled
Pamela Hinds, PhD, RNPrincipal InvestigatorChildren's National Health System

Eligibility Criteria

Age 18+ · All Participants · 0 Total Inclusion Criteria

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References

Frequently Asked Questions

Is this experiment in need of additional participants at the moment?

"Affirmative, the information hosted on clinicaltrials.gov verifies that this medical research is presently recruiting participants. The study was initially advertised on December 7th 2022 and its most recent update being February 1st 2023. There is a need for 221 patients to be enrolled at one centre." - Anonymous Online Contributor

Unverified Answer

What is the current recruitment rate for this experiment?

"Affirmative. Records hosted on clinicaltrials.gov divulge that this medical experiment, which was launched on December 7th 2022, is actively recruiting participants. Specifically, 221 patients must be sourced from a single centre of care." - Anonymous Online Contributor

Unverified Answer
Please Note: These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

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