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临床试验/NCT04245943
NCT04245943Unknown不适用

Rehabilitation - Physical Activity and Coping

Haukeland University Hospital2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2019年7月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
20
试验地点
2
主要终点
Objectively recorded physical activity level

研究概览

简要总结

The project is a non-randomized intervention study with group-based physical exercise. Cancer survivors who have participated in the rehabilitation program at the Center for Education and Rehabilitation are included in the study.

The cancer and cancer treatment have led to patients struggling with physical, mental and social late effects which prevent them from functioning in everyday life and return to work. The purpose of the project is to investigate whether one municipal group training measure can help to lower the threshold for the user to maintain good exercise habits and return to work / everyday life, as well as the effect on the user's physical form and quality of life and the transition between health level and the body itself measure.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

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

入选标准

  • Women and men
  • Regardless of cancer diagnosis
  • Resident in Bergen municipality
  • Finishes their rehabilitation at The Cancer Center for Education and Rehabilitation spring/summer 2019.

排除标准

  • Patients who do not speak or understand Norwegian
  • Unable to express themselves in writing
  • Unable to perform basic daily tasks
  • Display cognitive disorder or severe emotional instability
  • Suffer from other debilitating illnesses / conditions that may inhibit physical exercise (heart failure, chronic obstructive pulmonary disease, orthopedic conditions, neurological disorders or the like) will be excluded from the study. -

研究组 & 干预措施

Exercise

Experimental

18 weeks supervised strength and aerobic exercise training

干预措施: Exercise training (Behavioral)

结局指标

主要结局

Objectively recorded physical activity level

时间窗: 18 weeks

Change in objectively recorded physical activity level, measured with the SenseWear ™ Mini Armband (SWA) (BodyMedia Inc. Pittsburgh, PA, USA) as average minutes of moderate- to vigorous intensity physical activity (MVPA) from before intervention to after completion of the intervention.

次要结局

  • Change in maximal oxygen uptake measured by VO2max(18 weeks)
  • Change in maximal strength(18 weeks)
  • Change in quality of life measured by Short Form Health Survey (SF-36)(18 weeks)
  • Change in fatigue scores using the Chalder Fatigue Questionaire (FQ)(18 weeks)

研究者

发起方
Haukeland University Hospital
申办方类型
Other
责任方
Sponsor

研究点 (2)

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