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临床试验/NCT04145180
NCT04145180已完成不适用

3C-CUIDATE: Efectividad de un Programa de Recuperación Física en el Tratamiento de Las Secuelas Musculoesqueléticas, Funcionales y de Calidad de Vida en Pacientes de Cáncer de Cabeza y Cuello.

Universidad de Granada2 个研究点 分布在 1 个国家目标入组 55 人开始时间: 2019年9月2日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
55
试验地点
2
主要终点
Health-related quality of life

研究概览

简要总结

People receiving a head and neck cancer treatment often do not find an adequate therapeutic response for the side effects derived from this treatment. The objective of this study is to assess the effectiveness of a physical recovery program based on manual therapy over these problems.

Previous studies have shown the effectiveness of this type of programs on patients who have had cancer in other locations with clinically relevant results. There is a shortage of proposals for this subgroup of patients that require special attention. This project intends to carry out an experimental randomized controlled study with 84 patients treated of head and neck cancer who will be assigned randomly to the study groups: a) manual therapy program or, b) control group. The assessment refers to a baseline form (at the beginning of the study), at 6 weeks and at 6 months of patient follow-up.

详细描述

Manual therapy program consists of 3 sessions a week during 6 weeks, with a total of 18 appointments. Measurements are done before starting, after the last intervention and 6 months after finishing the treatment.

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
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • To have ended their treatment in the previous 6-24 months
  • To have no metastasis or active cancer
  • To have cervical and/or temporomandibular joint pain >3 in a Visual Analogue Scale

排除标准

  • Mental or physical illness preventing subjects from participating in the study
  • Previous chronic pain conditions
  • Previous cervical or temporomandibular joint pain
  • Previous dysphagia disorders

结局指标

主要结局

Health-related quality of life

时间窗: 6 weeks

Questionnaire EORTC QLQ-C30 was used for measuring quality of life

Pain Intensity

时间窗: 6 weeks

Visual Analogue Scale was used for evaluating pain intensity at cervical, temporomandibular joint, face and shoulder levels bilaterally. This consisted of a 10 cm horizontal line with the words "no pain" at the left extreme (0) and "pain as bad as it could be" at the right extreme (10)

Health-related quality of life - 2

时间窗: 6 weeks

Questionnaire EORTC QLQ-H\&N-35 was used for measuring quality of life specifically in survivors of head and neck cancer

Pressure pain thresholds

时间窗: 6 weeks

Pressure algometry (Force Dial DFK 20 analogue algometer, Wagner, Greenwich, USA) was assessed over the temporalis, masseter, upper trapezius and levator scapulae muscles and the C5-C6 zygapophyseal joint, the sternoclavicular joint and the tibialis anterior muscle as a distant reference muscle.

Shoulder and cervical active range of motion

时间窗: 6 weeks

Shoulder active range of motion (AROM) was assessed with a two-arms goniometer joined by a 360º protractor with the patient lying on a supine position. Cervical AROM was measured in a upright sitting position with a range of motion instrument (Performance Attainment Associates, Spine Products)

次要结局

  • Deep cervical flexors endurance(6 weeks)
  • Maximal mouth opening(6 weeks)
  • Perceived fatigue(6 weeks)
  • Sleep quality(6 weeks)
  • Sleeping disorders(6 weeks)
  • Anxiety(6 weeks)
  • Physical Fitness(6 weeks)
  • Temporomandibular disorders(6 weeks)
  • Shoulder pain and disability perception(6 weeks)
  • Isometric handgrip strength(6 weeks)
  • Fatigue(6 weeks)
  • Swallowing function(6 weeks)
  • Swallowing difficulty(6 weeks)

研究者

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

Carolina Fernández Lao

Dr. Carolina Fernández-Lao

Universidad de Granada

研究点 (2)

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