Phase 4
N=103
Reducing Suicidal Ideation Through Insomnia Treatment
Insomnia · Depression · Suicidal Ideation
Bottom Line
View on ClinicalTrials.gov: NCT01689909 ↗Enrolled (actual)
103
Serious AEs
1.0%
Results posted
Jun 2018
Primary outcome: Primary: Scale for Suicide Ideation Index (SSI) — 4.66; 5.25 units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 4
- Interventions
- Zolpidem-CR (Drug); Placebo (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Augusta University
- Primary completion
- Jun 2017
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Scale for Suicide Ideation Index (SSI) |
4.66; 5.25 | — |
| PRIMARY Columbia Suicide Severity Rating Scale (C-SSRS): the Suicidal Ideation Scale |
0.5447; 0.8067 | — |
| SECONDARY Dysfunctional Beliefs and Attitudes About Sleep |
6.03; 6.07 | — |
| SECONDARY Disturbing Dreams and Nightmares Severity Index (DDNSI) |
5.74; 6.44 | — |
| SECONDARY Beck Hopelessness Scale (BHS) |
9.40; 9.63 | — |
| SECONDARY Hamilton Rating Scale for Depression (HAM-D) |
14.93; 15.89 | — |
| SECONDARY Insomnia Severity Index (ISI) |
11.28; 13.72 | — |
Summary
Epidemiologic reports have linked insomnia to suicidal ideation and suicide death. However, no studies have determined whether treating insomnia decreases the risk of suicidality. We have new data indicating that (1) the link between insomnia and suicidal ideation holds true in clinical trials of depressed insomniacs, (2) dysfunctional cognitions about sleep are related to suicidal ideas, and (3) treatment of insomnia with hypnotics leads to a reduction of suicidal ideation. We now propose to test whether cautious use of hypnotics in suicidal, depressed insomniacs may reduce suicide risk in a multi-site clinical trial.
Eligibility Criteria
Inclusion Criteria
- Persons 18-65 years of age
- Persons with confirmed DSM-IV diagnosis of MDE by SCID
- Persons with Research Diagnostic Criteria diagnosis of insomnia
- Persons free of all psychotropic medications for one week before baseline assessment, except that prior FLX treatment will require 4 weeks of abstinence, and MAOIs will require 2 weeks of abstinence.
- Persons with Scale for Suicide Ideation (SSI) scores >2
- Persons with Hamilton Rating Scale for Depression (HRSD24) score >20
- Persons with Mini Mental State Exam (MMSE) score >24
- Persons with Insomnia Severity Index (ISI) score > 7
- Persons with habitual sleep latency > or = 30 minutes or wake time in the middle of the night of > or = 30 minutes, and sleep efficiency 3)
- Persons with clinical diagnosis of dementia
- Persons with active or past diagnosis of alcohol or substance abuse, bipolar disorder, schizophrenia per the SCID
- Persons who screen positive for moderate-severe sleep apnea (AHI >10) or a prior sleep laboratory-confirmed diagnosis of a primary sleep disorder, such as sleep apnea or periodic limb movement disorder.
- Persons with BMI > 50
- Persons with a self-reported history of napping > 2 times per week (as these are associated with sleep apnea and periodic limb movement disorder in depressed insomniacs)
- Persons who might be harmed by exposure to hypnotics, including pregnant women and patients with respiratory conditions
Data sourced from ClinicalTrials.gov (NCT01689909). 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.