The Effects of Preoperative Skin Traction and Position Splint on Pain, Comfort and Satisfaction in Patients With Hip Fracture
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 68
- 试验地点
- 2
- 主要终点
- Satisfaction from the treatment
研究概览
简要总结
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
- 50 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •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
排除标准
- •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
结局指标
主要结局
Satisfaction from the treatment
时间窗: Up to 7 days
Satisfaction from the treatment was assessed by VAS score from the next day after intervention till the surgery.
Pain
时间窗: 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.
Comfort
时间窗: 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.
次要结局
- Complications(Up to 7 days)
- Surgery duration(participants were followed for the duration of surgical procedure, an average of 2 hours)
- Hospitalization duration(participants were followed for the duration of hospital stay, an average of 2 weeks)
研究者
BETÜL TOSUN
RN, MsN, PhD
Saglik Bilimleri Universitesi Gulhane Tip Fakultesi