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O estudo clínico NCT06905951 (OSA) para Apneia Obstrutiva do Sono (AOS), Ronco, Qualidade do sono está recrutando. Consulte a visualização em cartões do Radar de Estudos Clínicos e as ferramentas de descoberta de IA para ver todos os detalhes. Ou pergunte qualquer coisa aqui.
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The Impact of Technology in Obstructive Sleep Apnea Myofunctional Therapy (OSA)

Recrutando
Os detalhes do estudo clínico estão disponíveis principalmente em inglês. No entanto, a IA Trial Radar pode ajudar! Basta clicar em 'Explicar o estudo' para visualizar e discutir as informações do estudo no idioma selecionado.
O estudo clínico NCT06905951 (OSA) é um ensaio intervencionista para Apneia Obstrutiva do Sono (AOS), Ronco, Qualidade do sono. Seu status atual é: recrutando. O estudo começou em 26 de agosto de 2024 e pretende incluir 34 participantes. Coordenado por a Universidade Case Western Reserve e deve ser concluído em 6 de dezembro de 2025. Essas informações foram atualizadas no ClinicalTrials.gov em 2 de abril de 2025.
Resumo
This is a study to test if performing airway exercises to improve snoring and sleep apnea using a mobile phone app is better than using a hardcopy guide.
Descrição detalhada
Outcomes will be measured using tone analysis, snoring recording apps, and oximeters.
Título oficial

The Impact Of Technology In The Myofunctional Therapy Treatment Of Obstructive Sleep Apnea Syndrome

Condições
Apneia Obstrutiva do Sono (AOS)RoncoQualidade do sono
Publicações
Artigos científicos e trabalhos de pesquisa publicados sobre este estudo clínico:
Outros IDs do estudo
  • OSA
  • STUDY20231615
Número NCT
Data de início (real)
2024-08-26
Última atualização postada
2025-04-02
Data de conclusão (estimada)
2025-12-06
Inscrição (estimada)
34
Tipo de estudo
Intervencionista
FASE
N/A
Status
Recrutando
Palavras-chave
OSA
Myotherapy
Myofunctional Exercises
Snoring
Sleep Apnea
Sleep Quality
Propósito principal
Tratamento
Alocação do design
Randomizado
Modelo de intervenção
Atribuição paralela
Cegamento (Mascaramento)
Nenhum (Estudo aberto)
Braços / Intervenções
Grupo de participantes/BraçoIntervenção/Tratamento
Comparador ativoApp Group
The mouth exercises are guided and tracked by a phone application.
EXERCÍCIO
Mouth, tongue, and throat exercise to strengthen the airway, reducing its collapsibility.
Comparador ativoAnalog Group
The exercise and tracking is done using paper forms.
EXERCÍCIO
Mouth, tongue, and throat exercise to strengthen the airway, reducing its collapsibility.
Desfecho primário
Medida de desfechoDescrição da medidaPrazo
Belun Ring Oxygen Saturation
Oximeter with pulse rate registration. The oximeter will provide the average level of oxygen saturation in the blood, provided in a percentage outcome. .
baseline and then monthly for 3 months.
Belun Ring lowest Oxygen Saturation Level
Oximeter with pulse rate registration. The oximeter will provide the lowest level of oxygen saturation recorded as a percentage.
baseline and then monthly for 3 months.
Belun Ring Oxygen Saturation under 70%
Oximeter with pulse rate registration. The oximeter will provide the percentage of sleep that was under 70% SpO2.
baseline and then monthly for 3 months.
Belun Ring AHI
Oximeter with pulse rate registration. The oximeter provides the Apnea/Hypopnea Index which is the number of apneic events per hour of sleep.
baseline and then monthly for 3 months.
Belun Ring Pulse Rate
Oximeter with pulse rate registration. The oximeter provides the pulse rate as the average beats per minute with standard deviation, and range.
baseline and then monthly for 3 months.
Desfecho secundário
Medida de desfechoDescrição da medidaPrazo
SnoreLab app
A mobile phone app that records snoring when present, and categorizes into amount and level. Possible outcomes are: none, mild, moderate, severe, and epic.
baseline and monthly for 3 months.
Tongue Elevation strength
The Iowa Oral Performance Instrument, is a validated intraoral device that measures tongue elevation strength in kPa.
baseline and monthly for 3 months.
Tongue Protrusion strength
The Iowa Oral Performance Instrument is a validated intraoral device that measures tongue protrusion strength in kPa.
baseline and monthly for 3 months.
Buccinator strength
The Iowa Oral Performance Instrument is a validated intraoral device that measure the buccinator muscle strength in kPa.
baseline and monthly for 3 months.
STOP-Bang Questionnaire
STOP-Bang is a validated tool that determines if the subject is at no, low, moderate, or severe risk of sleep-apnea. It provides an objective score that ranges from 0 to 8.
baseline and monthly for 3 months.
Nasal Obstruction Assessment (NOSE) Questionnaire Score
NOSE is a validated tool that determines the level of difficulty that the subject experienced in breathing through their nose in the past 3 months. The questionnaire provides an objective score stating the risk level that ranges from 0 to 100 with lower scores indicating less nasal blockage and higher scores indicating worse nasal blockage.
baseline and monthly for 3 months.
PROMIS Sleep Disturbance 8b Short Form Questionnaire
Assesses self-reported perceptions of sleep quality, sleep depth, and restoration associated with sleep. Each question usually has five response options ranging in value from one to five. Values are summed to generate a raw score that is then translated to a t-score with a mean of 50, std of 10.
baseline and monthly for 3 months.
Epworth Daytime Sleepiness Questionnaire
This is a validated tool that measures a person's daytime sleepiness and is commonly used to help diagnose sleep disorders. Eight prompts with each response scored from 0-3. Higher scores indicates greater sleepiness. It provides an objective score that can range from 0 to 24.
baseline and monthly for 3 months.
PROMIS Sleep Impairment 8a Short Form Questionnaire
Assesses self-reported perceptions of alertness, sleepiness, and tiredness during usual waking hours, and the perceived functional impairments during wakefulness associated with sleep problems or impaired alertness. Each question usually has five response options ranging in value from one to five. Values are summed to generate a raw score which is then translated to a t-score with a mean of 50, std of 10.
baseline and monthly for 3 months.
Critérios de elegibilidade

Idades elegíveis
Adulto, Adulto mais velho
Idade mínima
18 Years
Sexos elegíveis
Todos
  • Subjects with mild, moderate, and severe OSA who rejected/failed CPAP or other therapeutic options will be invited to participate in the study.

  1. Age lower than 18 or higher than 75.
  2. BMI > 40
  3. Alcoholism or drug abuse
  4. A-fib, pacemaker, CHF, strokes, narcotics
  5. Neuromuscular disease
  6. Use of benzodiazepine hypnotics (may affect muscle tone)
  7. Restricted tongue movement
  8. Permanently blocked nose
  9. TMJ disorder.
  10. Lost to follow-up
  11. Gained or lost ≥5% of body weight during 3 months
Case Western Reserve University logoUniversidade Case Western Reserve76 estudos clínicos ativos para explorar
American Association of Orthodontists Foundation logoAmerican Association of Orthodontists Foundation
Contato central do estudo
Contato: Juan M Palomo, DDS, MSD, 1-216-368-2449, [email protected]
Contato: Brittney Sullivan, DDS, 1-216-368-3249, [email protected]
1 Locais do estudo em 1 países

Ohio

Case Western Reserve University Dental Clinic - Orthodontics, Cleveland, Ohio, 44106, United States
Juan M Palomo, DDS, MSD, Contato, 216-368-2449, [email protected]
Juan M Palomo, DDS, MSD, Investigador principal
Recrutando