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临床试验/NCT07836842
NCT07836842尚未招募不适用

The Effect of Stress-Ball Distraction on Pain, Anxiety, Physiologic Responses, and Satisfaction During Painful Procedures in Critically Ill Patients: A Randomized Controlled Trial

Alexandria University0 个研究点目标入组 104 人开始时间: 2026年9月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
104
主要终点
Peak procedural pain intensity

研究概览

简要总结

This study will examine whether using a small hand-held stress ball during painful procedures can help critically ill adult patients feel less pain and anxiety. Painful procedures may also temporarily increase heart rate, blood pressure, and breathing rate.

Participants will be randomly assigned, like flipping a coin, to one of two groups. One group will receive usual care during the procedure. The other group will receive usual care and will be asked to squeeze a stress ball as a distraction technique during the procedure.

The study team will measure participants' pain and anxiety before, during, and 15 minutes after the procedure. The team will also record heart rate, blood pressure, respiratory rate, oxygen saturation, procedure-related events, use of additional pain medicine or sedation, and satisfaction with care. The findings may help health care providers understand whether stress-ball distraction is a safe, simple, non-drug method for improving comfort during painful procedures in critically ill patients.

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
None

入排标准

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

入选标准

  • •Adults aged ≥18 years admitted to the critical care unit.
  • •Patients scheduled for a painful procedure, including arterial puncture, venipuncture, tracheal suctioning, repositioning, or dressing change.
  • •Patients able to provide informed consent.
  • •Patients able to use the pain and anxiety rating scales.

排除标准

  • •Cognitive impairment preventing reliable self-report.
  • •Severe hand injury or neuromuscular disorder.
  • •Hemodynamic instability.
  • •Allergy to stress-ball materials.

研究组 & 干预措施

Standard care

Active Comparator

Participants will receive the usual standard care provided during the painful procedure, without stress-ball distraction.

干预措施: Standard care (Other)

Stress-Ball Distraction

Experimental

Participants will receive standard care during the painful procedure and will use a hand-held stress ball as a distraction technique.

干预措施: Stress-Ball Distraction (Other)

结局指标

主要结局

Peak procedural pain intensity

时间窗: During the painful procedure

Pain intensity will be assessed using the 0-10 Numeric Rating Scale (NRS), where 0 indicates no pain and 10 indicates the worst pain imaginable. The peak pain score recorded during the painful procedure will be compared between the stress-ball distraction and standard-care groups.

次要结局

  • State anxiety during the painful procedure(During the painful procedure)
  • Patient satisfaction with the procedure and pain management(15 minutes after the painful procedure)
  • Heart rate during and after the painful procedure(Baseline before the procedure (T0), during the procedure (T1), and 15 minutes after the procedure (T2))
  • Systolic blood pressure during and after the painful procedure(Baseline before the procedure (T0), during the procedure (T1), and 15 minutes after the procedure (T2))
  • Diastolic blood pressure during and after the painful procedure(Baseline before the procedure (T0), during the procedure (T1), and 15 minutes after the procedure (T2))
  • Respiratory rate during and after the painful procedure(Baseline before the procedure (T0), during the procedure (T1), and 15 minutes after the procedure (T2))
  • Peripheral oxygen saturation (SpO₂) during and after the painful procedure(Baseline before the procedure (T0), during the procedure (T1), and 15 minutes after the procedure (T2))

研究者

申办方类型
Other
责任方
Sponsor

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