跳至主要内容
临床试验/TCTR20230816008
TCTR20230816008已完成2 期

The effectiveness of telehealth intervention on functional status, anxiety, and depression and the number of rehospitalizations among elders with Coronary Artery Bypass Graft (CABG) surgery: A randomized controlled trial

ASSOC.PROF.USAVADEE ASDORNWISED, Major Advisor0 个研究点目标入组 84 人开始时间: 2023年8月16日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
84

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
60 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • The eligible participants will be recruited in the study if they have any criteria described as follows: 1) are at least 60 years and scheduled to receive first-time elective isolated CABG; 2) have functional class I-III following New York Heart Association (NYHA) class 50 ; 3) have a primary family caregiver willing to participate in the study; 4) can access and use a smartphone via an internet connection either with or without assistance from the primary family caregiver; 5) able to communicate in the Thai language; 6) have no cognitive impairment (A cut-off point of 3 from 5 by Thai version Mini-cog).

排除标准

  • The eligible participants will be excluded from the study if they have severe dementia, Alzheimer's disease, delirium, terminal illness, or psychiatric disorders, which be diagnosed by a physician. The participants will be withdrawn from the study if they have any criteria described as follows: 1) are admitted to a nursing home and have barriers to participating in the program; 2) refuse to participate after involvement in the intervention or if they want to withdraw their participation in the study; 3) have no report of the physical measures and symptoms back to the researcher for five consecutive days, and the researcher can not contact the participants by telephone call over three consecutive days; 4) have cardiac arrest during the operation; 5) have severe complications after CABG surgery, such as stroke, renal failure, and require ongoing renal dialysis.

研究者

发起方
ASSOC.PROF.USAVADEE ASDORNWISED, Major Advisor

相似试验