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临床试验/NCT05287932
NCT05287932已完成不适用

A Pilot Randomised Controlled Trial of a Brief Physical Activity Intervention in Older People With Multimorbidity

Northumbria University1 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2022年5月9日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
1
主要终点
Average daily acceleration

研究概览

简要总结

Physical activity is an important determinant of health and well-being in older people. However, many older people do not achieve recommended physical activity levels and increasing older people's physical activity is challenging. This preliminary study will explore the effects of a brief physical activity intervention on physical activity and physical function in older people with multimorbidity. The findings will be used to inform the design of a subsequent adequately-powered randomised controlled trial.

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 (Outcomes Assessor)

盲法说明

Outcome assessors will be blinded to group allocation, and participants will be asked to not disclose their allocation

入排标准

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

入选标准

  • aged ≥60 years
  • 2 or more chronic conditions
  • able to walk outside the home
  • able to attend the study visits

排除标准

  • living in a residential or nursing home
  • housebound
  • ≥3 falls in previous year
  • dementia or significant cognitive impairment (unable to follow simple instructions)
  • contraindication to increasing physical activity
  • unable to read or speak English
  • unable to provide consent
  • no more than one person per household

研究组 & 干预措施

Intervention

Experimental

Brief physical activity intervention including an initial 45-minute physical activity consultation, telephone support after 2 weeks (approx. 15-minute call), and provision of a pedometer, written information, and a physical activity diary. Embedded behaviour change techniques will include goal setting, self-monitoring, building self-efficacy and social support, and overcoming barriers.

干预措施: Brief physical activity intervention (Behavioral)

Wait-list control

No Intervention

The control group will not receive any active or placebo intervention during the 4-week study period. They will also not receive any trial contacts during this period. They will however continue to be able to access their usual care from primary, secondary, community, and social services. After the final (4-week) follow-up assessment, this group will receive the full physical activity intervention.

结局指标

主要结局

Average daily acceleration

时间窗: 4 weeks

Average acceleration from wrist accelerometry

次要结局

  • Intensity gradient(4 weeks)
  • Time in MVPA(4 weeks)
  • Steps(4 weeks)
  • 30-second chair rise performance(4 weeks)
  • Timed 8ft up and go performance(4 weeks)
  • Timed single-leg balance performance(4 weeks)
  • Muscle strengthening exercise(4 weeks)
  • Handgrip strength(4 weeks)
  • 6-minute walk test performance(4 weeks)

研究者

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

Garry Tew

Professor Garry Tew

Northumbria University

研究点 (1)

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