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N/A N=25 Health Services Research

Nurse Suicide: Physiologic Sleep Health Promotion Trial

Suicide · Nurse's Role · Work Environment Adverse Effects · Sleep · Stress

Enrolled (actual)
25
Serious AEs
0.0%
Results posted
Nov 2024
Primary outcome: Primary: Columbia Suicide Severity Rating Scale (Intensity of Ideation) - Number of Participants With a Positive CSSRS Ideation — 2 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
PureSomni Sleep Health Product Kit (Behavioral)
Age
Adult, Older Adult · 21+ yrs
Sex
All
Sponsor
Columbia University
Primary completion
Sep 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Columbia Suicide Severity Rating Scale (Intensity of Ideation) - Number of Participants With a Positive CSSRS Ideation
PRIMARY
Columbia Suicide Severity Rating Scale (Intensity of Ideation) - Number of Participants With a Positive CSSRS Ideation
PRIMARY
Columbia Suicide Severity Rating Scale (Intensity of Ideation) - Number of Participants With a Positive CSSRS Ideation
PRIMARY
Physiologic Stress Response- Heart Rate Variability [Group Mean Difference Between Week 1-4(Control) and Week 5-8(Intervention)]
0.846
PRIMARY
Perceived Sleep Quality Via Pittsburgh Sleep Quality Index Global Sleep Score (Group Mean)
5.85
PRIMARY
Perceived Sleep Quality Via Pittsburgh Sleep Quality Index Global Sleep Score (Group Mean)
5.85
PRIMARY
Perceived Sleep Quality Via Pittsburgh Sleep Quality Index Global Sleep Score (Group Mean)
5.85
PRIMARY
Physiologic Sleep Data - Sleep Duration (Mean Daily Hours)
6.81
PRIMARY
Number of Participants With at Least 1 Suicidal Behavior (Frequency)
SECONDARY
Burnout Screening Via Maslach Burnout Inventory (Subscale 1: Emotional Exhaustion) - Mean Composite Score
29
SECONDARY
Burnout Screening Via Maslach Burnout Inventory (Subscale 2: Depersonalization) - Mean Composite Score
10.88
SECONDARY
Burnout Screening Via Maslach Burnout Inventory (Subscale 3: Personal Accomplishment) - Mean Composite Score
44.92
SECONDARY
Burnout Screening Via Maslach Burnout Inventory (Subscale 1: Emotional Exhaustion) - Mean Composite Score
29
SECONDARY
Burnout Screening Via Maslach Burnout Inventory (Subscale 2: Depersonalization) - Mean Composite Score
10.88
SECONDARY
Burnout Screening Via Maslach Burnout Inventory (Subscale 3: Personal Achievement) - Mean Composite Score
44.29

Summary

The purpose of this study is to identify factors (sleep, psychiatric characteristics, stressful life events, and work environment characteristics) that potentiate or mitigate adverse effects of real-world stressors that predispose nurses to suicidal risk. The specific aims are: Aim 1. To investigate associations between sleep, stressful life events (life stressors, discrimination, lateral violence), psychiatric characteristics (psychiatric diagnosis, subjective mood), work environment characteristics (workload, shift type and duration, overtime, nurse work environment, and team relations) and stress (self-report and heart rate variability) in working nursing professionals while controlling for standard covariates known to influence stress. Aim 2. To determine if stress exposure (self-report and HRV) is associated with predisposing factors (sleep, stressful life events, additional psychiatric characteristics, and work environment characteristics), and to explore whether stress mediates the effect of predisposing factors on suicidal ideation in working nursing professionals. Exploratory Aim. To explore the preliminary impact of an existing sleep intervention (sleep health promotion kit) on self-reported stress, HRV, sleep, and psychiatric health outcomes including depression, burnout, and suicidal ideation. This record will focus on the Exploratory Aim.

Eligibility Criteria

Inclusion criteria

  • currently practicing as a registered nurse in the clinical setting
  • have worked continuously in the same position for at least 1 year
  • read, speak, and understand English language

Exclusion criteria

  • >1-month sick leave in the past 3 months
  • pregnancy (known physiologic stress confounder)
  • other healthcare workers (e.g., physicians).
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT06079853). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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