NCT07669870

Brief Summary

the purpose of this study is to evaluate and compare the effectiveness of using low level laser therapy versus oropharyngeal exercises in the treatment of snoring in patient diagnosed with obstructive sleep apnea. the study aims to determine which intervention provide better clinical outcome in reducing snoring severity and improve sleep quality

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
180

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Jan 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 1, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2026

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

June 5, 2026

Completed
16 days until next milestone

First Submitted

Initial submission to the registry

June 21, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

June 25, 2026

Completed
Last Updated

June 25, 2026

Status Verified

June 1, 2026

Enrollment Period

4 months

First QC Date

June 21, 2026

Last Update Submit

June 21, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • snoring severity and risk using the berlin questionnaire

    the Berline questionnaire is used to assess the risk and severity and obstructive sleep apnea .it consist of 3 categories addressing the severity of snoring, day time sleepiness, and history of high blood pressure or obesity changes in the questionnaire scores will be evaluated to compare the clinical outcome between the groups

    6 weeks

Study Arms (3)

laser therapy group

EXPERIMENTAL

patients in this group received low level laser therapy targeting soft palate and surrounding upper airway tissues

Device: low level laser therapy

orophrgeal exercises

EXPERIMENTAL

patient in this group performed oropharyngeal exercises and tongue exercises to strengthen upper air way

Behavioral: oropharyngeal exercises

control group

NO INTERVENTION

patient in this group didn't receive any active exercises or laser they receive only advices

Interventions

laser applications to the oral mucosa and soft palate tissue

laser therapy group

structured myofunctional and tongue strengthening exercises for snoring reduction

orophrgeal exercises

Eligibility Criteria

Age40 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Patient are clinically and medically stable 2-Patients are able to understand and follow the instruction 3-Patient 's age range from 40 to 55 years old 4-Patient are male and females 5-Patient have snoring due to diagnostic mild sleep apnea disorder 6- BMI of patients ranging from (30 - 34.9) Obesity Class I and obesity class 2 ( 35-39)
  • Exculsioncriteria :
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  • In stability of patient 's medical condition 3-In ability to comprehered and follow instruction as in dementia or speech proplems such as dysphasia 4-Patients with cognitive disorders 5-Patients with musculoskeletal and neurological problems 6- patients with diabetes

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Physcial Therapy Cairo Unvirsity

Cairo, Egypt

Location

MeSH Terms

Conditions

Sleep Apnea, ObstructiveSnoring

Interventions

Low-Level Light Therapy

Condition Hierarchy (Ancestors)

Sleep Apnea SyndromesApneaRespiration DisordersRespiratory Tract DiseasesSleep Disorders, IntrinsicDyssomniasSleep Wake DisordersNervous System DiseasesRespiratory SoundsSigns and Symptoms, RespiratorySigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Laser TherapyTherapeuticsPhototherapy

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
physiotherapist

Study Record Dates

First Submitted

June 21, 2026

First Posted

June 25, 2026

Study Start

January 1, 2026

Primary Completion

May 1, 2026

Study Completion

June 5, 2026

Last Updated

June 25, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

to maintain participant confidentiality and comply with the regulation of the institutional research ethical committee

Locations