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A prospective clinical study on improving sleep structure and quality by regular training of air-conditioned exercise system guided by cardiopulmonary coupling technology in the treatment of nocturnal hypertension

A prospective clinical study on improving sleep structure and quality by regular training of air-conditioned exercise system guided by cardiopulmonary coupling technology in the treatment of nocturnal hypertension

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000035395
Enrollment
Unknown
Registered
2020-08-10
Start date
2020-12-06
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Nocturnal hypertension

Interventions

Morning group:Exercise + medicine
16 pm group:Exercise + medicine
19 pm group:Exercise + medicine

Sponsors

Shanghai Tongji Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Patients aged 25-60 years old will be selected for 24-hour ambulatory blood pressure monitoring, and then screened according to the standard of national hypertension prevention and treatment guidelines in 2018; 2. Patients with nocturnal blood pressure will be enrolled; 3. The nighttime blood pressure of the selected patients: systolic blood pressure 150-120 mmHg, diastolic blood pressure: 70-95 mmHg.

Exclusion criteria

Exclusion criteria: 1. cardiac function was higher than grade III (NYHA); 2. Combined with unstable angina pectoris; 3. acute myocardial infarction; 4. various arrhythmias; severe renal insufficiency; 5. respiratory failure; recent cerebral infarction and cerebral hemorrhage; 6. cerebrovascular accident with severe limb movement disorder; 7. severe respiratory disease; 8. tumor; 9. hematological diseases; The experiment will be terminated immediately if the blood pressure rises more than 180 / 120mmhg, cerebrovascular accident, acute myocardial infarction, malignant arrhythmia, unstable angina pectoris, and aggravation of cardiac and renal insufficiency. If the patient still can't carry out training according to the experimental plan after three times of supervision, it will be regarded as automatic loss.

Design outcomes

Primary

MeasureTime frame
nocturnal blood pressure;Total sleep time;Sleep efficiency;

Countries

China

Contacts

Public Contactfanghong

Shanghai Tongji Hospital

de_61@163.com+86 021 66111048

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026