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临床试验/CTRI/2026/03/106360
CTRI/2026/03/106360尚未招募不适用

Efficacy of Chin Tuck Against Resistance (CTAR) exercise on level of dysphagia among post-extubated patients in selected ICU of a tertiary care hospital, Bhubaneswar- a Randomized Controlled Trial

MEGHA CHAKRABORTY1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年3月31日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1

研究概览

简要总结

This randomised controlled pre-test post-test study aims to evaluate the effectiveness of the Chin Tuck Against Resistance (CTAR) exercise on the level of dysphagia among post-extubated ICU patients in a tertiary care hospital in Bhubaneswar. A total of 60 participants (30 intervention, 30 control) will be included based on predefined inclusion and exclusion criteria. The intervention group will perform CTAR exercises using a 12.5 cm towel roll for 5 sets, thrice daily for 7 days, while the control group will receive routine dysphagia care. Swallowing ability will be assessed using standardised tools before and after the intervention. Computerised randomisation and single blinding will be used to reduce bias, and allocation will be concealed using opaque methods. Data will be analysed using descriptive and inferential statistics, including paired and unpaired t-tests. The study is expected to demonstrate a significant improvement in swallowing function among patients receiving CTAR exercises. As a safe, simple, and affordable bedside intervention, CTAR may help accelerate oral intake recovery and reduce dysphagia-related complications in post-extubated ICU patients.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant Blinded

入排标准

年龄范围
25.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Adults aged from 25 to 60 years are post-extubated ICU patients.
  • Patients a minimum of 6 hours after extubation following at least 48 hours of endotracheal intubation in the ICU of PBMH, Bhubaneswar.
  • Patient who has an RASS score between 0 and 2 in the post-extubation phase.
  • Willing to participate in the study.
  • Ability to comply with the interventions and communications.

排除标准

  • Patients who are in tracheostomy.
  • Patients who have any head and neck injury, chest injury, or rib fracture.
  • Pre-existing dysphagia due to a pre-existing neurological disorder.

研究者

发起方
MEGHA CHAKRABORTY
申办方类型
Other [SELF FUNDED]
责任方
Principal Investigator
主要研究者

Megha Chakraborty

Kalinga Institute of Industrial Technology

研究点 (1)

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