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临床试验/NCT04168658
NCT04168658Unknown不适用

A Pilot and Feasibility Cluster Randomized Controlled Trial of Physical Activity Program for Female Nursing Home Residents at Risk of Osteoporosis

Chengdu Jinjiang Maternity and Child Health Hospital0 个研究点目标入组 80 人开始时间: 2020年2月10日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
80
主要终点
Change of habitual physical activity

研究概览

简要总结

Worldwide, osteoporosis causes more than 8.9 million fractures per annum. Osteoporosis used to be a significant public health concern that most commonly affected Caucasian women in Northern Europe and the United States. Recently, it has become a major public health problem in Asia, most notably among Chinese women.

We intend to conduct a cluster randomized controlled trial (RCT) to examine if a physical activity and education intervention, compared with an education-only intervention (waiting list for physical activity), can result in improved physical activity, reduced falls, and maintaining bone mass, among female nursing home residents in China. The aim of the current pilot and feasibility trial is to test the feasibility and acceptability of conducting these interventions.

A pilot and feasibility cluster RCT will be conducted for females aged 60 to 75 years living in nursing homes in Chengdu, the capital of Sichuan Province, Western China. The unit of cluster randomization is the nursing home. A total of four nursing homes (two state-owned and two private-owned) will be involved in the pilot and feasibility trial. They will be randomly selected and afterwards randomly assigned to either the intervention group (2 nursing homes) or control group (2 nursing homes). We seek to recruit 20 women from each nursing home.

The intervention group participants will exercise with the research staff or under supervision of the trained nursing home staff, and will receive face-to-face workshops, booklet, newsletters, phone calls, and short message service (SMS) reminders. Participants in the control group will only receive educational materials (i.e. face-to-face workshops and booklet) and will be wait listed to receive no other interventions of this study until after the post-intervention. All participants will be referred to doctors for advice and standard care as usual.

The primary outcome is the change of habitual physical activity from baseline to 12 months, which will be measured using the International Physical Activity Questionnaire - Short Form (IPAQ-SF). Secondary outcomes include incidental falls and change in bone mineral density (BMD) from baseline to 12 months. The study results will serve to provide an estimate of the effect size, intraclass correlation coefficient (ICC) and rates of eligibility, recruitment and attrition, which may enable a more accurate sample size calculation for a definitive RCT.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Single (Outcomes Assessor)

入排标准

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

入选标准

  • (cluster level-nursing home):
  • have at least 100 female residents aged 60 to 75 years

排除标准

  • (cluster level-nursing home):
  • are participating in any other clinical trials
  • Inclusion Criteria (participant level):
  • aged 60 to 75 years
  • Exclusion Criteria (participant level):
  • have a previous diagnosis of osteoporosis
  • are osteoporotic
  • are taking medicines that would affect calcium or bone metabolism
  • are already physically active (i.e. exercise at least three times a week at a moderate or higher intensity for ≥ 30 min)
  • have taken part in any physical activity program within the past year
  • sustain any medical condition that would put them at risk by taking part in moderate intensity exercises

结局指标

主要结局

Change of habitual physical activity

时间窗: Baseline to 12 months post-baseline

The primary outcome is the change of habitual physical activity from baseline to 12 months, which will be measured using the International Physical Activity Questionnaire - Short Form (IPAQ-SF).

次要结局

  • Incidental falls(12 months starting from the baseline)
  • Change in bone mineral density (BMD)(Baseline to 12 months post-baseline)

研究者

发起方
Chengdu Jinjiang Maternity and Child Health Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Li Tang

Assistant Professor

Chengdu Jinjiang Maternity and Child Health Hospital

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