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临床试验/NCT05691803
NCT05691803已完成不适用

Understanding Motivation Towards Exercise to Enhance Physical Activity on Prescription Adherence - Feasibility Study

Umeå University2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2023年2月3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
20
试验地点
2
主要终点
Adherence to the exercise intervention

研究概览

简要总结

The goal of this clinical trial is to explore feasibility and evaluate methods to investigate changes in physical activity, function and psychometrics in relation to an exercise intervention in physically inactive middle-aged men and women. The main questions it aims to answer are:

  • Is the exercise intervention feasible regarding retention and user experience?
  • Is the evaluation methods on physical activity, function and psychometrics suitable for the present study?
  • Is there an intervention effect in physical activity, function and psychometrics at three and six month post baseline?
  • Can barriers and facilitators towards increased physical activity be identified in the two groups of the study?

All participants will first receive standard care for physically inactive patients, i.e. Physical activity on Prescription (PaP), followed by allocation to an exercise intervention (EI) group. The EI group will be offered an additional exercise intervention for 12 weeks consisting of 1-2 training sessions per week of a combination of aerobic and resistance training at a private fitness center.

Feasibility of the exercise intervention will be evaluated based on retention rates and user experience.

Additionally, researchers will assess physical activity, function and psychometrics in the EI group at three and six months to evaluate the suitability of the chosen methods and to get preliminary data on the intervention effect. Finally, interviews with the participants in the control and EI groups will be performed at the end of the study in order to explore barriers and facilitators towards increased physical activity in formally inactive patients.

Edit after registration of the study: Due to a lower number of recruited participants than expected (20 instead of the anticipated 30), the protocol was updated by removing the control group that would initially consist of 10 participants. The remaining 20 participants were all allocated to the exercise intervention group to assess feasibility of the intervention.

研究设计

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

入排标准

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

入选标准

  • Physically inactive persons as defined as not meeting the current recommendations of at least 150 minutes of moderate to vigorous physical activity per week. This criterion is self-assessed by potential participants.
  • Age 40-60 years

排除标准

  • Physical disability that affects the ability to perform the exercise intervention.
  • Heart failure or severe degenerative disease, e.g. malignant cancer, multiple sclerosis etc.
  • Myocardial infarction or stroke during the last 12 months.
  • Heart conditions including angina pectoris that is worsened with exercise.
  • Neuromuscular, musculoskeletal, or rheumatic conditions that is worsened with exercise.
  • Hypertension grade III, i.e. systolic blood pressure above 180 mmHg and/or diastolic blood pressure over 110 mmHg.

结局指标

主要结局

Adherence to the exercise intervention

时间窗: Documented continuously during the 12 week intervention period

Number of completed training sessions in the exercise intervention group

Retention rate

时间窗: 3 months post baseline

The proportion of participants starting the intervention that completes outcome assessment in either group

次要结局

  • Daily step-count(Baseline, 3 months and 6 months)
  • Time spent in moderate and vigorous physical activity(Baseline, 3 months and 6 months)
  • Health related quality of life(Baseline, 3 months and 6 months)
  • Motivational stages of self-determination for exercise(Baseline, 3 months and 6 months)
  • Lower limb muscle strength(Baseline, 3 months and 6 months)
  • Confidence in one's own ability to exercise(Baseline, 3 months and 6 months)
  • Cardio-respiratory capacity(Baseline, 3 months and 6 months)
  • Upper limb strength(Baseline, 3 months and 6 months)
  • Self-reported exercise and physical activity(Baseline, 3 months and 6 months)
  • Basic psychological needs connected to physical activity satisfaction(3 months and 6 months)

研究者

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

Andreas Hult

Associate Professor

Umeå University

研究点 (2)

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