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临床试验/NCT05390138
NCT05390138尚未招募不适用

A Smart Sleep Apnea Self-management Support Programme(4S) to Improve Apnea Severity and Cardiovascular Health - A Pragmatic Randomized Controlled Trial With Mixed-method Evaluation

The University of Hong Kong0 个研究点目标入组 120 人开始时间: 2022年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
120
主要终点
Change in apnea hypopnea index

研究概览

简要总结

OSA is a chronic disease with high prevalence that parallels with increasing obesity. Self-management programmes are perceived to be cost-effective in long-term OSA patient care and can supplement regular medical treatments. The current study attempt to examine the effectiveness of 4S on improving apnea severity, cardiovascular health and quality of life in 4S intervention (4S) group, compared to the general hygiene (GH) control group.

详细描述

OSA is a chronic disease with high prevalence that parallels with increasing obesity. OSA affects around 12% and 24% of adults in Hong Kong and China Mainland, respectively. Chronic intermittent hypoxia and sleep fragmentation of OSA leads to cardiometabolic and neurocognitive sequelae (e.g. hypertension, diabetes, daytime sleepiness and depression). Long-term, multidisciplinary management involving patients in decision-making of treatment strategies, shifting from positive airway pressure (PAP) device-focused to the patient-centered chronic care model has been suggested.

Mobile instant messaging (such as WhatsApp/WeChat) are popular and inexpensive for interactive messaging. Smartphone-based self-management interventions were reported improved self-efficacy and clinical outcomes in patients with chronic diseases. The investigator only found one mobile health application to support CPAP therapy for OSA and one ongoing trial of OSA self-management telematic support to improve CPAP adherence. There is underutilization of mobile technology in patient-centered self-management programmes to improve PAP treatment and lifestyle modifications in OSA.

The current study attempt to examine the effectiveness of 4S on improving apnea severity, cardiovascular health and quality of life in 4S intervention (4S) group, compared to the general hygiene (GH) control group. Questionnaire and simple fitness assessment will be used to assess the effectivness of the intervention at 4-month and 12-month follow-up. Focus group interview will be conducted to collect qualiatative feedback on the intervention.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

盲法说明

The outcome assessor did not aware of which groups the patients belongs to.

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • aged 18 years and above;
  • diagnosis of moderate to severe obstructive sleep apnea (AHI≥15);
  • physically inactive (self-reported moderate physical activity per week of <150 minutes);
  • overweight (BMI≥23 kg/m2);
  • mentally, cognitively and physically fit to join the trial as determined by the doctor in-charge and responsible clinical investigators;
  • able to speak and read Chinese;
  • willing to complete the questionnaires and assessments;
  • has a smartphone with instant messaging function (eg. WhatsApp/WeChat); and
  • willing to give informed consent.

排除标准

  • sleep disorder other than OSA;
  • clinically significant psychiatric, neurological, or medical disorder other than OSA; and
  • use of prescription drugs or clinically significant drugs affecting sleep.

结局指标

主要结局

Change in apnea hypopnea index

时间窗: Baseline, 4 months

Apnea hypopnea index will be asssessed by sleep test. The apnea hypopnea index is the number of times of apnea or hypopnea during one night, divided by the hours of sleep. The higher the apnea hypopnea index, the more severe sleep apnea is.

次要结局

  • Change in body weight(Baseline, 4 months and 12 months)
  • Change in body neck circumference(Baseline, 4 months and 12 months)
  • Change in apnea hypopnea index(Baseline and 12 months)
  • Change in Duration of <90% oxygen desaturation(Baseline, 4 months and 12 months)
  • Change objective physical activity level(Baseline, 4 months and 12 months)
  • Change in lower limb strength(Baseline, 4 months and 12 months)
  • Change in flexibility(Baseline, 4 months and 12 months)
  • Change in balance(Baseline, 4 months and 12 months)
  • Change in daytime sleepiness(Baseline, 4 months and 12 months)
  • Change in sleep quality(Baseline, 4 months and 12 months)
  • Change in dietary habits(Baseline, 4 months and 12 months)
  • Change in self-efficacy in CPAP use(Baseline, 4 months and 12 months)
  • Change in body fat(Baseline, 4 months and 12 months)
  • Change in functional outcomes of sleep(Baseline, 4 months and 12 months)
  • Change in depressive symptoms(Baseline, 4 months and 12 months)
  • Change in subjective happiness(Baseline, 4 months and 12 months)
  • Change in waist circumference(Baseline, 4 months and 12 months)
  • Change in hip circumference(Baseline, 4 months and 12 months)
  • Change in subjective physical activity level(Baseline, 4 months and 12 months)
  • Intervention credibility(4 months and 12 months)
  • Change in exercise and dietary control self-efficacy(Baseline, 4 months and 12 months)
  • Change in perceived support from family and peers(Baseline, 4 months and 12 months)
  • Change in Hand grip strength(Baseline, 4 months and 12 months)
  • Change in quality of life(Baseline, 4 months and 12 months)
  • Change in anxiety symptoms(Baseline, 4 months and 12 months)
  • Change in patient activation(Baseline, 4 months and 12 months)

研究者

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

Dr. Agnes Yuen-Kwan Lai

Assistant Professor

The University of Hong Kong

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