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Promoting Walking in Older Adults Living in Independent Living Communities in Northern Ireland: A Feasibility Study.

2017年9月18日 更新者:Dr Mark Tully、Queen's University, Belfast
The multi-level 12 week peer-led walking intervention incorporates aspects from all three levels of the ecological model (with the aim of producing sustained (>6months) physical activity behaviour change in older adults living in independent living communities.

研究概览

详细说明

The proposed study is a cluster randomized controlled feasibility trial of a multi-level peer-led walking intervention. The socio-ecological model and social cognitive theory provides the framework that will help inform and test the feasibility of a multi-level peer-led walking intervention for inactive older adults living in independent living communities in Northern Ireland. The behaviour change techniques identified and extracted from a previous systematic review on the effectiveness of peer-led physical activity interventions helped guide the decision-making process of which behavior change strategies should be included in this study. The logic model helped inform the design and development of the 12 week peer-led walking programme.

研究类型

介入性

注册 (预期的)

60

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Belfast、英国、BT12 6BJ
        • Centre for Public Health, Queen's University Belfast

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

55年 及以上 (成人、年长者)

接受健康志愿者

是的

有资格学习的性别

全部

描述

Inclusion Criteria:

  1. Adults over the age of 60 years recruited from fold housing associations, dependent on site; those receiving nursing care will not be included.
  2. Inactive/not regularly walking (less than 30 minutes
  3. Have the ability to read, write, understand and speak English.
  4. Can walk freely without human assistance (residents will be included they use a walking stick/walking aid.)

Exclusion Criteria:

  1. If they have fallen in the last 6 months
  2. Have regular nursing assistance/care within the fold
  3. Residents with dementia or other cognitive challenges will be excluded.

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:预防
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:Intervention
They will complete a 12-week peer-led walking programme. Participants will be paired together as walking partners and will be given a pedometer and step count logs for self-monitoring. The walking co-ordinators will facilitate walking groups two times a week in the local areas, lasting for 30 minutes. The nature of the walks will be tailored to the participants stated preferences of types of activity. Participants will also receive local walking route maps. After 12 weeks, the formal peer-led component will finish and participants will be encouraged to continue walking with their walking partners other activity programmes organised in the fold in order to maintain activity levels.
A 12 week peer led walking group for adults and older adults (> 55 years) living in independent living communities in Northern Ireland. Designed to increase physical activity levels of inactive older adults and measure sustained changes in physical behaviour 6 months after the intervention ends.
无干预:Control

Folds assigned to the control group will not receive any additional support to change their physical activity behaviour over the course of the intervention period.

At the six-month data collection point they will be offered a referral to a local walking group in their area or advice on beginning a self-directed walking programme (similar to Public Health Agency www.choosetolivebetter.com/content/getting-active). They will be asked to complete outcome measures at baseline and follow up time-points. Post-study a sample of control participants will be asked to attend a focus group, exploring their views on social activity as form of physical activity for older adults in folds.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Moderate-to-vigorous physical activity (MVPA)
大体时间:Baseline, 12 weeks and 6 months
Changes from baseline MVPA as assessed by Actigraph accelerometer
Baseline, 12 weeks and 6 months

次要结果测量

结果测量
措施说明
大体时间
Quality of Life
大体时间:Baseline, 12 weeks and 6 months
To explore changes in health-related quality of life, a validated self-reported questionnaire EuroQol-5D will be completed by study participants.
Baseline, 12 weeks and 6 months
Self-efficacy
大体时间:Baseline, 12 weeks and 6 months
Changes in self-efficacy will be measured using a short version of exercise behaviour self-confidence questionnaire.
Baseline, 12 weeks and 6 months
Physical and Mental Health
大体时间:Baseline, 12 weeks and 6 months
Changes in other health-related and well-being outcomes will include completing the (7 item) Warwick-Edinburgh Mental Well-being score.
Baseline, 12 weeks and 6 months
Social Engagement
大体时间:Baseline, 12 weeks and 6 months
Changes in social engagement will be measured using the Lubben social network scale
Baseline, 12 weeks and 6 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Mark A Tully, PhD、Queen's University, Belfast

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始

2015年9月1日

初级完成 (实际的)

2016年9月1日

研究完成 (实际的)

2016年9月1日

研究注册日期

首次提交

2015年11月2日

首先提交符合 QC 标准的

2015年11月2日

首次发布 (估计)

2015年11月4日

研究记录更新

最后更新发布 (实际的)

2017年9月19日

上次提交的符合 QC 标准的更新

2017年9月18日

最后验证

2017年9月1日

更多信息

与本研究相关的术语

其他研究编号

  • 15.30

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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