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Skin Traction Versus Position Splint in Patients With Hip Fracture

2014年11月6日 更新者:BETÜL TOSUN、Saglik Bilimleri Universitesi Gulhane Tip Fakultesi

The Effects of Preoperative Skin Traction and Position Splint on Pain, Comfort and Satisfaction in Patients With Hip Fracture

The aim of this prospective, randomized controlled trial is to compare the effects of preoperative skin traction and position splint on pain, comfort, complications, difficulty level of nursing interventions, satisfaction from treatment and nursing care in patients with hip fracture. The sample is comprised of 34 patients with hip fracture in each group, totally 68 patients. Skin traction and position splint were applied after block randomization. Data regarding pain, comfort, satisfaction from care, immobilization comfort, complications, time of operation and hospitalization time were collected after intervention.

研究概览

研究类型

介入性

注册 (实际的)

68

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Ankara、火鸡、06018
        • Gülhane Military Medical Academy

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

50年 及以上 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Being inpatient who were planned the surgery due to the hip fracture (caput femur fracture, collum femur fracture, femur intertrochanteric fracture and subtrochanteric fracture) diagnosis in the Orthopedics and Traumatology Clinic
  • Being 50 years old or more
  • Patients who speak and literate in Turkish
  • Patients who gave informed consent to participate in the study

Exclusion Criteria:

  • Any condition that emerges an obstacle for verbal and written interaction during data collection phase
  • Unable to perform written or verbal communication in Turkish
  • Withdrawal from the study due to medical reasons or death, at his/her will prior to preoperative data collection
  • Urgent non-elective surgery
  • Physician decision that do accept the method of immobilization assigned to the patient as appropriate

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:支持治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
有源比较器:Skin traction
Prior to hip fracture surgery, affected limb was wrapped with a special elastic bandage and pulled from the sole of the foot with a weight of 5-10% of total body weight of the patient (min 2.3 kg, max 4.5 kg).
This group is the routine treatment (control) valid in the clinical practice.
实验性的:Position splint
Prior to hip fracture surgery, position splint was applied to the affected limb in order to keep the extremity in the proper positon without any weight lifting.
This group is the actual intervention group.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Pain
大体时间:up to 7 days
Pain was assessed by VAS score prior to intervention, 15, 30, 60 and 120 minutes after intervention and daily from the next morning of intervention till the surgery.
up to 7 days
Comfort
大体时间:up to 7 days
Comfort was assessed by VAS score prior to intervention, 15, 30, 60 and 120 minutes after intervention and by Immobilization Comfort Questionnaire daily from the next morning of intervention till the surgery.
up to 7 days
Satisfaction from the treatment
大体时间:Up to 7 days
Satisfaction from the treatment was assessed by VAS score from the next day after intervention till the surgery.
Up to 7 days

次要结果测量

结果测量
措施说明
大体时间
Complications
大体时间:Up to 7 days
Complications (pressure ulcer, deep vein thrombosis, allergic skin reaction, pulmonary and urinary tract infection and constipation due to immobilization) were evaluated daily after intervention till the surgery.
Up to 7 days
Surgery duration
大体时间:participants were followed for the duration of surgical procedure, an average of 2 hours
Time that the surgical procedure has taken was assessed.
participants were followed for the duration of surgical procedure, an average of 2 hours
Hospitalization duration
大体时间:participants were followed for the duration of hospital stay, an average of 2 weeks
Time spent in the hospital till discharge was assessed.
participants were followed for the duration of hospital stay, an average of 2 weeks

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Betul Tosun, RN, PhD、Saglik Bilimleri Universitesi Gulhane Tip Fakultesi
  • 学习椅:Ozlem Aslan, Assoc.Prof.、Saglik Bilimleri Universitesi Gulhane Tip Fakultesi

出版物和有用的链接

负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。

一般刊物

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2013年3月1日

初级完成 (实际的)

2014年4月1日

研究完成 (实际的)

2014年7月1日

研究注册日期

首次提交

2014年11月3日

首先提交符合 QC 标准的

2014年11月6日

首次发布 (估计)

2014年11月10日

研究记录更新

最后更新发布 (估计)

2014年11月10日

上次提交的符合 QC 标准的更新

2014年11月6日

最后验证

2014年11月1日

更多信息

与本研究相关的术语

关键字

其他研究编号

  • B.10.4.İSM.4.06.68.49/

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

在美国制造并从美国出口的产品

不

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