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Effect of adjustment of sleeping and head position on snoring and OSA severity

Effect of adjustment of sleeping and head position on snoring and OSA severity

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123734
Enrollment
Unknown
Registered
2026-04-29
Start date
2026-05-31
Completion date
Unknown
Last updated
2026-05-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sleep snoring, apnea, obstructed airway during sleep

Interventions

Baseline-treatment 1 group:Adjust the head, shoulder, and neck posture during sleep by changing the shape of the inflatable pillow. Night 1 is the baseline, Night 2 head tilted backward 10°, head rota
Baseline-treatment 3 group:Adjust the head, shoulder, and neck posture during sleep by changing the shape of the inflatable pillow. The first night serves as the baseline, and on the second night, the
Baseline-treatment 2 group:Adjust the head, shoulder, and neck posture during sleep by changing the shape of the inflatable pillow. The first night serves as the baseline, with the head tilted back 20
Baseline-treatment 4 group:Adjust the head, shoulder, and neck posture during sleep by changing the shape of the inflatable pillow. The first night serves as the baseline, and on the second night, the

Sponsors

Bejing Tongren Hospital, Capital Medical Uniersity
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Adults aged 18-65; 2. Completed polysomnography at a sleep medicine center due to symptoms such as snoring, apnea, or daytime sleepiness, without receiving systematic treatment; 3. Diagnosed with habitual snoring or mild to moderate obstructive sleep apnea (AHI <30 events/hour); 4. Subjects are able to understand and sign the informed consent form and comply with the trial protocol.

Exclusion criteria

Exclusion criteria: 1.Hearing, visual impairment, or serious mental illness; 2.Severe cardiovascular, cerebrovascular, metabolic and respiratory diseases, cervical spondylosis or limited neck activity; 3.Pregnant and lactating women; 4.Any situation that the investigator considers unsuitable for participating in the trial;

Design outcomes

Primary

MeasureTime frame
Apnea-Hypopnea Index;Snoring Index;

Secondary

MeasureTime frame
Side-sleep Ratio;Awakening Count;

Countries

China

Contacts

Public ContactLi Yanru

Bejing Tongren Hospital, Capital Medical Uniersity

liyanruru@aliyun.com+86 10 5826 9325

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026