跳至主要内容
临床试验/CTRI/2024/06/068690
CTRI/2024/06/068690尚未招募不适用

A comparison between smartphone version with traditional paper version of visual analogue pain scale for pain assessment in children

Anushree Mohan A1 个研究点 分布在 1 个国家目标入组 125 人开始时间: 2024年6月21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
125
试验地点
1
主要终点
Assessment of postoperative pain: The participant will self report the pain using both the paper VAS and the smartphone version at T0 and T1. The pain will be assessed at rest and with activity. If the participant reports pain score

研究概览

简要总结

“Pain is an unpleasant sensory & emotional experience associated with actual or potential tissue damage” with multiple dimensions.

Poorly controlled post-operative pain has a number of negative consequences for the patient such as delay in functional recovery, hospital discharge and increased risk of chronic pain.

The visual analogue pain scale is a well recognized & validated self- report scale in children & adults and its use has been validated in children above 7 years.

The electronic pain assessment tools have the potential to promote compliance, co-operation, consistency in results & promote better communication between healthcare professionals, pediatric patients and their care givers.

Primary aim of the study is to compare the smartphone version of visual analogue pain scale with the traditional paper version in the assessment of pain in children and the secondary objective is to determine the child preference for the smart phone version or the hardcopy version of the tool

研究设计

研究类型
Observational

入排标准

年龄范围
7.00 Year(s) 至 18.00 Year(s)(—)
性别
All

入选标准

  • Children of ASA 1-3 status undergoing surgery and a planned post surgical recovery in Postanaesthetic Care Unit (PACU).

排除标准

  • Children Unwilling to participate Children with Neurological injury, psychomotor dysfunction Children with significant visual or hearing impairment.

结局指标

主要结局

Assessment of postoperative pain: The participant will self report the pain using both the paper VAS and the smartphone version at T0 and T1. The pain will be assessed at rest and with activity. If the participant reports pain score

时间窗: The first(T0) set of pain assessment will take place in the PACU when the participant is fully awake as deemed appropriate for assessment by the bedside nurse. | The second (T1) set of pain assessment will be performed when the participant is fit for discharge from the PACU

≥40 at rest, pain assessment on activity will not be conducted.

时间窗: The first(T0) set of pain assessment will take place in the PACU when the participant is fully awake as deemed appropriate for assessment by the bedside nurse. | The second (T1) set of pain assessment will be performed when the participant is fit for discharge from the PACU

次要结局

  • The child’s preference for the smart phone version or the hardcopy version of the tool.(The preference will be assessed when the child is fit to be discharged from Postoperative Care Unit (T1))

研究者

发起方
Anushree Mohan A
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Anushree Mohan A

Kasturba Medical College Manipal

研究点 (1)

Loading locations...

相似试验