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临床试验/NCT07181980
NCT07181980尚未招募不适用

Effect of Intercostal Mulligan Moblization on Shoulder Dysfunction Post Mastectomy

Cairo University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年9月16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
40
试验地点
1
主要终点
range of motion of shoulder abducation Universal goniometer.

研究概览

简要总结

the study is to evaluate the therapeutic efficacy of intercostal mulligan Mobilization in decreasing pain and improve ROM for shoulder dysfunction Patients post mastectomy.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Participant)

入排标准

年龄范围
40 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients post modified radical mastectomy at least 3 months prior and had a limited ROM in abduction.
  • •Patients post mastectomy with lateral chest wall pain.
  • •Age ranges between 40-60 years.
  • •All patients had informed written consent

排除标准

  • •Receiving any previous rehabilitation programs for the upper extremities
  • •The presence of any type of metastases
  • •The presence of lymphedema
  • •Bilateral breast cancer surgery
  • •Locoregional recurrence
  • •Withdrawal of the consent at any time during the study for any reason

研究组 & 干预措施

intercostal mulligan moblization

Active Comparator

干预措施: Exercise (Other)

intercostal mulligan moblization

Active Comparator

干预措施: Intercostal mulligan mobilization with shoulder abduction (Other)

control group

Active Comparator

干预措施: Exercise (Other)

结局指标

主要结局

range of motion of shoulder abducation Universal goniometer.

时间窗: Universal goniometer: maximum pain free shoulder abduction was investigated in an upright position .Normal range of active movement of the shoulder 180 degree Were recorded at baseline and at the end of 8 weeks of treatment.

次要结局

  • 1.4.a. Measuring shoulder function The Arabic version of DASH questionnaire(The DASH was adapted into Arabic . contains 30 items , each item has five response choices that range from 1, ''without any difficulty or no symptoms exist'' to 5, ''.Were recorded at baseline and at the end of 8 weeks of treatment)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Aya Medhat Nagib Abd Elhakim

Submitted In Partial Fulfilment of The Requirements For Master Degree In Department of Physical Therapy for surgery Cairo university

Cairo University

研究点 (1)

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