Intraoral Tongue Stimulation for Treatment of Primary Snoring

Signifier Medical Technologies

Status: Completed

Conditions: Snoring; Obstructive Sleep Apnea

Treatments: Device: Intraoral tongue stimulator (Snoozeal)

Study type: Interventional

Funder types: Industry

Identifiers

NCT03829956

Snoozeal

Details and patient eligibility

About

Intraoral Neuromuscular Training for Treatment of Snoring

Objective

Studies show that improving pharyngeal muscle tone can ameliorate obstructive sleep apnoea (OSA) and snoring. The study uses an intra-oral stimulation device (SnooZeal) aimed at a population of snorers. The aim of this study is to assess the efficacy of intra-oral neuromuscular stimulation training during wakefulness on snoring.

Methods

This is a prospective study, recruiting up to 200 patients from the sleep clinics.

In this study, subjects will use the intra-oral stimulation device once a day for 20 minutes each time for a period of 6 weeks. During these 6 weeks, subjects will complete a daily diary of the device use and any side effects or adverse events. Partners also complete a daily snoring score.

Subjects will be followed-up for a further 2 weeks after treatment. They will complete Pittsburgh Sleep Quality Index (PSQI) and subjective sleep quality questionnaires for a further 2 weeks. Partners will also complete the post treatment snoring scores. Sleep study will be repeated.

Outcome measures

The objective evaluation will be based on pre- and post-treatment sleep studies, visual analogue scale (VAS) snoring scores, PSQI and subjective sleep quality questionnaire. All side effects and adverse events will be reported and acted upon according to the risk management structure.

Full description

Aim/ Objective

The aim of this study will be to assess the efficacy of transoral neuromuscular stimulation training during wakefulness on snoring.

Patients and Methods

This is a prospective observational study, recruiting patients from the sleep clinics at the Department of Otorhinolaryngology, Head and Neck Surgery in Queen's Hospital, Barking, Havering and Redbridge University Hospitals National Health Service (NHS) Trust

Sample size planned is up to 200 participants.

Study Protocol

A. Screening Participants will be identified from Queen's Hospital, Barking, Havering and Redbridge NHS Trust. There will be a screening phone call to ensure suitability based on an inclusion criterion and offer first line information about the trial. If suitable, participants will be given a written information sheet and invited to undertake a 2 day home sleep study (using WatchPAT). If the average apnea-hypopnea index (AHI) from these 2 days is below 15/h, the participants will be invited for a clinical examination.

B. Recruitment visit

• Clinical airway examination by Ear, Nose and Throat (ENT) consultant
• Review of inclusion and exclusion criteria
• Informed consent
• Inclusion into trial

C. Pre-therapy period (day -14 to -1):

• Bed partner daily subjective assessment of snoring (Visual Analogue Scale - participant's bed partner will be required to complete daily visual analogue scoring of the participant's snoring, with 1 being "no snoring" and 10 being "intolerable snoring")
• Oral examination (detailed examination by dentist to document pre-therapy oral state
• Participant and bed partner to complete sleep quality questionnaires (Pittsburgh Sleep Quality Index, Epsworth sleepiness score (ESS) and subjective sleep quality questionnaire) on Day -1

D. Therapy phase (day 1-42)

• Face-to-face meeting, instruction on use of the intraoral device
• Participant to use the Snoozeal device for 20 minutes once daily
• Bed partner daily subjective assessment of snoring (VAS)
• Participant daily assessment of side effects/adverse events and time of use
• Participant and bed partner to complete Sleep quality Questionnaires (Pittsburgh Sleep Quality Index, Epsworth sleepiness score and subjective sleep quality questionnaire) at day 42
• Weekly follow up phone call from research team to confirm compliance. Compliance will also be cross checked using the total time of use recorded by the device.

E. End of Therapy Review (day 43 - 49)

• Review of device integrity by visual inspection
• Oral examination (detailed examination by dentist to document post therapy oral state)
• Repeat Sleep Study - 2 night sleep study with WatchPAT

F. Follow Up phase (day 43-56)

• Participant advised to stop using device
• Bed partner daily subjective assessment of snoring (VAS)
• Subject and bed partner to complete Sleep quality Questionnaires (Pittsburgh Sleep Quality Index, Epworth sleepiness score and subjective sleep quality questionnaire) at day 56

G. Post Therapy Review (day 57)

• Face-to-face meeting and feedback
• Collection of participant data sheets
• Participant subjective overall assessment

Data Analysis

The pre and post sleep studies will be performed using WatchPAT. Parameters recorded: saturation, AHI, snoring sound parameters.

AHI will be identified and analyzed by WatchPAT data and software. The WatchPat is an approved FDA sleep study device. Snoring will be quantified subjectively by both the bed partner using a visual analog score, and objectively during the home sleep study as frequency of snores (number of snores / hours of sleep) and % total sleep time spent snoring. Sleep quality will be quantified subjectively by PSQI score. Sleepiness will be quantified subjectively by ESS score.

Enrollment: 115 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age 18 years and above at entry into study
• Subjects must have a live-in partner
• > 6 months history of habitual snoring (>5 days per week)

Exclusion criteria

• Body Mass Index > 35
• Apnoea-Hypopnoea Index >15
• Symptomatic nasal pathology
• Tonsil Hypertrophy (Tonsil size > Grade 2)
• Tongue or lip piercing
• Pacemaker or implanted medical electrical devices
• Previous oral surgery for snoring
• Relevant facial skeletal abnormalities
• Certain oral disease/conditions (see Appendix 3)
• Any criteria that, in the opinion of the investigator, would make the participant unsuitable for the study due to inability to complete required study procedures

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

---

115 participants in 1 patient group

Snoring and mild OSA

Other group

Description:

This cohort of participants has been diagnosed with primary snoring or mild obstruction sleep apnoea. A medical device (intra-oral tongue stimulation device) will be introduced for 6 weeks and the effects will be assessed by comparing the outcome measures before and after the intervention.

Treatment:

Device: Intraoral tongue stimulator (Snoozeal)