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临床试验/CTRI/2024/04/066140
CTRI/2024/04/066140已完成不适用

Effectiveness of transcutaneous electrical nerve stimulation in addition to routine physiotherapy care on quality of life and pain after abdominal hysterectomy: A Randomized Controlled Trial.

Priyadharshini R1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2024年5月23日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
32
试验地点
1
主要终点
Abdominal surgery impact scale

研究概览

简要总结

Effectiveness of Transcutaneous Electrical Nerve Stimulation in addition to Routine Physiotherapy care on Quality of Life and Pain after Abdominal hysterectomy: A Randomized Controlled Trial.

After the Abdominal hysterectomy the incisional pain is more ,it causes the negative impact of the patient physical and mental health. Post operative pain reduce the Quality of Life. The preferred post operative pain is opioid usage. However due to opioid- related side effects, including emesis and itiching , opioid use can lead to poor Quality of Life ,Thus, contemporary pain therapy aims to reduce opioid usage via multimodal technique. includes Breathing exercises, Coughing techniques, Circulatory exercises, Knee rolling, log rolling, patient made to sit, Abdominal exercises, Pelvic tilting, Getting in and out of the bed, Pelvic floor exercises and mobilization around the ward, outside the ward and stair climbing, All the exercises were performed. Transcutaneous Electrical Nerve Stimulation is non invasive, non pharmacological and low frequency electrotherapy technique has been used for pain after Abdominal hysterectomy. There is a lack of awareness about Transcutaneous Electrical Nerve Stimulation (TENS) usage in addition to Routine physiotherapy care. There is a urgent need for research on the Effectiveness of Transcutaneous Electrical Nerve Stimulation in addition Routine Physiotherapy care improve Quality of Life and reduce Pain after Abdominal hysterectomy. Outcome measure used for Abdominal Surgery Impact Scale (ASIS), and Visual Analogue Scale (VAS)

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
35.00 Year(s) 至 55.00 Year(s)(—)
性别
Female

入选标准

  • Women undergoing Abdominal hysterectomy in OG I unit OT days (Wednesday & Saturday) in their postoperative days 1 to
  • Willing to participate in the study.
  • Pain score ≥3 measured by the Visual analogue scale (VAS) / pain of 5 or greater on a 0 to 10 numerical rating scale (NRS) or moderate on a verbal descriptive scale were approached to participate in the study.

排除标准

  • Preoperative opioid use (regular use of opioid analgesics for more than 2 weeks during the 6 month period before surgery as determined by patient interview).
  • Inability to cognitively follow the required directions.
  • Participator’s inability to fully complete with study protocol due to uncontrolled epilepsy, Renal failure, Cardiopulmonary disorders, Central nervous system disease (or) psychosis.
  • Coagulation disorders.
  • Any sign of sepsis.
  • Any specialties surgery of the head (brain, face), neck ( Thyroid, throat) Thoracic (cardio , pulmonary) , breast, Orthopaedic including amputations (or) reset of amputation (phantom limb pain) , (or) Plastic surgery (Liposuction) were not considered.
  • Any skin allergy(dermatological lesions affecting electrode placement).

结局指标

主要结局

Abdominal surgery impact scale

时间窗: Outcome taken from post operative day 1 and post operative day 6

次要结局

  • Visual analogue scale(Post operative day 1 before & after intervention)

研究者

发起方
Priyadharshini R
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

PRIYADHARSHINI R

Mother Theresa Post Graduate and Research Institute of Health science (Government of Pondicherry)

研究点 (1)

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