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临床试验/NCT01255436
NCT01255436已完成不适用

Effectiveness of SMS Text Reminders to Improve Blood Pressure Among Patients With Hypertension at a General Medicine Outpatient Clinic in a Tertiary Center in Manila, Philippines: A Randomized Controlled Trial

University of the Philippines2 个研究点 分布在 1 个国家目标入组 700 人开始时间: 2011年1月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
700
试验地点
2
主要终点
Mean Absolute Change in Systolic Blood Pressure After 12 Weeks

研究概览

简要总结

Objective: To test the primary hypothesis that SMS text messages delivered to patients via mobile phone can improve blood pressure within 12 weeks compared to usual care

Design: Parallel group, randomized, controlled trial; the patient is the unit of randomization

Setting: General Medicine Outpatient Continuity Clinic of the Philippine General Hospital and Private Outpatient Clinics near the Philippine General Hospital

Patients: Ambulatory men and women aged 19 years and older (N=700) with a diagnosis of essential hypertension, on maintenance blood pressure-lowering medications, who have daily access to a mobile phone in the household and know or live with someone who knows how to retrieve, read and reply to text messages using a mobile phone

Intervention: SMS text messages delivered twice a week for 12 weeks, which aim to 1) provide information regarding hypertension; 2) remind patients to take their medications.

Main Outcome Measure: The primary outcomes are the mean change in systolic and diastolic blood pressures at the end of 12 weeks. The secondary outcomes are improvement in blood pressure control rate and medication adherence.

详细描述

The study will be done in 2 phases:

Phase I: Development of the SMS text messages

The SMS messages to be used in the trial will be developed and pre-tested in focus group discussions of a convenience sample of subjects similar to the target population for understandability and acceptability.

Phase II: Parallel group, open-label, randomized, controlled trial

Target Population

研究设计

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

入排标准

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

入选标准

  • Ambulatory adult patients of both sexes with age at least 19 years old being seen at the General Medicine Outpatient Clinic of the Philippine General Hospital
  • A diagnosis of hypertension in the medical record
  • On at least 1 maintenance medication for hypertension for at least 1 month
  • A systolic blood pressure greater than 129 mmHg and less than 160 mmHg or a diastolic blood pressure greater than 79 mmHg or less than 100 mmHg at the time of screening
  • Patients with daily access to a mobile phone in the household
  • Patients who live with someone who knows how to retrieve and read text messages on their mobile phone, and can relay these messages to them
  • Written informed consent

排除标准

  • Participation in other studies within one month of trial initiation
  • Patients who are unable or refuse to give informed consent
  • Patients who have a clinical condition that might interfere with the study (dementia, psychological disorder)
  • Patients who share a household with another patient who has already been recruited to participate in this study

结局指标

主要结局

Mean Absolute Change in Systolic Blood Pressure After 12 Weeks

时间窗: baseline and 12 weeks

Absolute change in systolic blood pressure from baseline to 12 weeks

Mean Absolute Change in Diastolic Blood Pressure After 12 Weeks

时间窗: baseline and 12 weeks

Absolute change in diastolic blood pressure from baseline to 12 weeks

次要结局

  • Medication Adherence Rate(12 weeks)
  • Percentage of Patients With Controlled Blood Pressure at the End of 12 Weeks(12 weeks)

研究者

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

Lia M. Palileo

Clinical Associate Professor

University of the Philippines

研究点 (2)

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