Clinical Trials Directory

Trials / Completed

CompletedNCT01281332

Mechanical Device for the Relief of Hot Flashes

Evaluation of a Novel Mechanical Device for Relief of Menopausal Vasomotor Symptoms.

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Queen's University · Academic / Other
Sex
Female
Age
40 Years – 65 Years
Healthy volunteers
Accepted

Summary

Hypothesis: A mechanical device when applied to the back of the neck at the onset of a menopausal hot flash will attenuate the severity and duration of symptoms providing women with a reassuring non-hormonal intervention to improve quality of life in the menopausal transition. This pilot study will evaluate the effectiveness of this unit. The mechanism of action of the device will not be revealed in advance.

Detailed description

This is a pilot study to test logistics and gather information for planning the definite trial. We will randomly allocate 40 subjects to receive either the active Menopod device (n=20) or a sham device with the mechanism disabled (n=20). We will recruit menopausal women with moderate to severe hot flashes (as defined by FDA standards this means a minimum of 7 per day). The two primary outcome parameters are the hot flash score which is the product of frequency x intensity (Sloan 2001), and the average duration (in minutes) of hot flash episodes over the course of one day. These outcomes will be self-recorded by subjects in a diary designed by our research team on five separate days throughout the course of the study, once during the evaluation phase and once per week over the four week treatment phase. The two summary measures will be the changes from baseline to the last record collected for hot flash scores and average durations. Delta values (assessment phase minus fourth treatment period) will be compared between the two treatment groups (active versus sham device) using t tests (IBM SPSS Statistics version 21).

Conditions

Interventions

TypeNameDescription
DEVICEMenopodThe mechanism of action of the device will not be revealed in advance.
DEVICEInactive device

Timeline

Start date
2013-09-01
Primary completion
2014-08-01
Completion
2014-08-01
First posted
2011-01-21
Last updated
2015-09-11

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01281332. Inclusion in this directory is not an endorsement.