Trial · NCT04253691
Sleep Intervention for Chronic Insomnia Using Virtual Reality Pilot Study
NCT04253691, Not applicable, Active not recruiting, University of Missouri-Columbia
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Sleep Intervention for Chronic Insomnia Using Virtual Reality Pilot Study. Trials, record NCT04253691. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04253691
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Sleep Intervention for Chronic Insomnia Using Virtual Reality Pilot Study
- NCT number
- NCT04253691
- Status
- Active not recruiting
- Phases
- Not applicable
- Enrollment
- 30 participants, actual
- Lead sponsor
- University of Missouri-Columbia
- Conditions
- Insomnia Chronic, Pain, Chronic
- Interventions
- Virtual Reality Mediated Relaxation
- First posted
- 2020-02-05
- Last updated
- 2026-04-22
Source ClinicalTrials.gov
Registered outcomes14
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Daily Electronic Sleep/Pain Diaries | 6 weeks | Daily electronic dairies will record pain intensity and unpleasantness, sleep (latency, wake after onset, efficiency, quality), fatigue, sleep and pain medication consumption |
| Primary | Objective Daily Sleep Actiwatch-2 (Wake After Sleep Onset) | 6 weeks | Objective wake after sleep onset |
| Primary | Objective Daily Sleep Actiwatch-2 (Sleep Onset Latency) | 6 weeks | Objective sleep onset latency |
| Primary | Objective Daily Sleep Actiwatch-2 (Sleep Efficiency) | 6 weeks | Objective sleep efficiency |
| Primary | Insomnia Severity Index | 6 weeks | Insomnia severity measurement; min: 0 max:28; higher score means greater insomnia severity |
| Primary | Fatigue Severity Scale | 6 weeks | Fatigue severity; min:10 max: 73; higher score means higher fatigue severity |
| Secondary | Patient centered outcomes questionnaire | 6 weeks | The Patient Centered Outcomes questionnaire assesses four domains (pain, fatigue, emotional distress, and interference with daily activities) relevant to chronic pain populations on a numerical rating scale ranging from 0-10; min: 0 max:200; 200; A greater score equates a worse outcome |
| Secondary | Computerized Cognitive Assessments -WCST | 6 weeks | Determine level of cognitive functioning |
| Secondary | Computerized Cognitive Assessments - Stroop Task | 6 weeks | Determine level of cognitive functioning |
| Secondary | Computerized Cognitive Assessments - Sternberg tasks | 6 weeks | Determine level of cognitive functioning |
1 to 10 of 14Source ClinicalTrials.gov
See all 14 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as |
|---|---|
| 30087642 | BACKGROUND |
Source PubMed
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests3
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Card Sorting Test (Berg) | Secondary outcome | ConductCognition |
| Sternberg Memory Scanning | Secondary outcome | ConductCognition |
| Stroop Color-Word Test | Secondary outcome | ConductCognition |
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT04253691
GET https://conductscience.org/api/trials/v1/NCT04253691/registered