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NCT01378793: AcuSnooze

Acupressure for Insomnia

Terminated NA Last updated 6 February 2017
What this trial tests

NA trial testing Relaxation Acupressure in Insomnia in 5 participants. Terminated before completion.

Timeline
15 June 2011
Primary endpoint
15 December 2013
15 December 2013

Quick facts

Lead sponsorUniversity of Michigan
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposetreatment
Enrollment5
Start date15 June 2011
Primary completion15 December 2013
Estimated completion15 December 2013
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

University of Michigan

Who can join

Adults 18 to 65, any sex, with Insomnia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to examine the effect of 6-weeks of relaxation acupressure compared to stimulating acupressure or a standard of care on sleep and daytime functioning. Also, to evaluate the ability of teaching acupressure using web-based applications. It is believed that self-administered relaxation acupressure will result in improvements of sleep quality and quantity as compared to stimulating acupressure or a standard of care.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Insomnia

Currently open trials in the same condition.

Other University of Michigan trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01378793.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing