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临床试验/NCT05077748
NCT05077748已完成不适用

An 18-year Follow-up Study on Obstructive Sleep Apnoea in a Population-based Cohort

Chinese University of Hong Kong1 个研究点 分布在 1 个国家目标入组 202 人开始时间: 2021年10月20日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
202
试验地点
1
主要终点
OSA status at 18-year follow-up visit

研究概览

简要总结

Our research team has established a polysomnography (PSG) quantified population-based paediatric sleep cohort in 2003 for a childhood OSA prevalence study. Subjects were recruited from 13 randomly selected primary schools. All subjects from this original cohort will be invited to join this 18-year follow-up study to repeat the following data collection: questionnaires, anthropometric measurement, sleep study, 24-hour ambulatory blood pressure (ABP) measurement, echocardiography and neurocognitive assessment.

详细描述

Our research team has established a polysomnography (PSG) quantified population-based paediatric sleep cohort in 2003 for a childhood OSA prevalence study. Subjects were recruited from 13 randomly selected primary schools. In each school, two randomly chosen classes from each grade were invited to participate. In the first phase, all parents of children in the randomly selected schools were invited to attend an education forum during which full explanation of the purpose and flow of the study was given. An envelope containing a validated parent proxy OSAS screening questionnaire and consent was then distributed to parents within a week after the forum. From our previous research, a composite symptom score (summation of the scores of these three questions) of 7 or more has 75.4% sensitivity and 80.5% specificity, compared with polysomnography, to detect OSAS among children aged 5-15 years who had attended our paediatric clinics. Children with a composite symptom score of less than 7 were assigned a computer-generated random number and were invited as a control group with a ratio of 1:2 in the second phase. All children belonging to the high risk of OSAS group and the randomly selected subjects at low risk of OSAS were invited to participate the baseline epidemiological study. In total 619 children aged 5-13 years underwent detailed assessments including anthropometric measurements, airway examination, ambulatory blood pressure recording and overnight PSG. 67 children had moderate-to-severe OSA (obstructive apnoea hypopnoea index, OAHI ≥5/h), 199 had mild OSA (OAHI 1 to <5/h), 103 were primary snorers (OAHI <1/h but snore ≥3 nights per week in the past 12 months) and 250 were normal controls (OAHI <1/h and snore <3 nights per week in the past 12 months).(1) All subjects from this original cohort will be invited to join this 18-year follow-up study to repeat the following data collection: questionnaires, anthropometric measurement, sleep study, 24-hour ambulatory blood pressure (ABP) measurement, echocardiography and neurocognitive assessment.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • - Subjects participants from the 2003 cohort

排除标准

  • Neuromuscular disease
  • Pathological central apnoea
  • Severe chronic lung disease with documented hypoxaemia or awake oxygen saturation <92%
  • Chronic respiratory failure (unrelated to OSA)
  • Acquired upper airway disease/obstruction
  • Craniofacial abnormalities (e.g. secondary to trauma and malignancy)
  • Other arrangement:
  • Subjects who have any respiratory illness within 2 weeks of the scheduled follow-up visit will have their assessment re-arranged until they have fully recovered.
  • Subjects taking medications that may affect sleep, upper airway patency or blood pressure (for example sedatives, stimulants, antihistamines, and cough medicine) within a week from recruitment will also be rescheduled to participate when they are free from medication use for at least 2 weeks.
  • Subjects with hypertension and are on anti-hypertensive therapy are allowed to continue on their medication and the information will be obtained and recorded during data collection.

结局指标

主要结局

OSA status at 18-year follow-up visit

时间窗: Through study completion, an average of 2 years

OSA status of the participants at the 18-year follow-up visit

次要结局

  • Factors associated with the persistence or the development of OSA in adulthood(Through study completion, an average of 2 years)
  • Ambulatory blood pressure parameters at 18-year follow-up visit(Through study completion, an average of 2 years)
  • Echocardiographic parameters at 18-year follow-up visit(Through study completion, an average of 2 years)
  • Neurocognitive function at 18-year follow-up visit(Through study completion, an average of 2 years)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kate Ching Ching Chan

Clinical Professional Consultant, Department of Paediatrics

Chinese University of Hong Kong

研究点 (1)

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