A Pain Self-management Program for Older Adults: Online vs. Workbook Delivery
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 121
- 试验地点
- 2
- 主要终点
- Change in chronic pain severity
研究概览
简要总结
It is well documented that severe pain is more common in older adults than it is younger persons. Of concern, older adults may not have access to traditional face-to-face self-management programs, which are recognized to be valuable in chronic pain management. Access to effective self-management approaches is particularly important for older adults who may have mobility limitations or live in remote areas, or have difficulty accessing health care services. The development of effective pain self-management programs for older adults who cannot access traditional psychological interventions is of significant importance. Internet self-management programs have the potential to address pain undermanagement. As technology advances, the digital divide between the older and younger demographic continues to progress. Given the known difficulties with treatment access, the purpose of this study is to explore the efficacy and acceptability of a remotely-delivered chronic pain self-management program tailored to older adults, the Pain Course, when delivered in online and workbook formats. The program was previously shown to be effective among younger persons but has not been tested with older adults.
详细描述
The program is delivered through a secure platform administered by the Online Therapy Unit for Service Education and Research at the University of Regina. Using a patient preference randomized control trial (RCT) design, participants (n = 120) will be enrolled in either the online group or workbook group, or to a wait list control group. The content of both programs will be identical and contain 5 core lessons, which participants will be encouraged to work through over an 8-week period. By exploring the efficacy of an online vs. workbook group, the results from this study may serve as a stepping-stone for improved self-management of chronic pain in older adults.
A patient preference randomized controlled trial (RCT) was chosen for this study. The goal is to have most participants accept randomization by emphasizing they are equally acceptable, so only those with a very strong preference or no access to Internet aren't randomized. According to the preliminary power analysis, a total of 120 participants will be randomly assigned to be enrolled in the online group or workbook group, or be placed on a twelve-week wait list control, which will serve as a control group to control for the influence of time on symptom change between groups.
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
- None
入排标准
- 年龄范围
- 65 Years 至 —（Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •are residents of Canada
- •are 65 years of age or older
- •report experiencing pain for more than three months
- •are not experiencing very severe symptoms of depression or anxiety
- •have regular access to a computer and the internet
- •are proficient in writing and speaking the English language
排除标准
- •high suicide risk
- •concerns about online therapy
- •not present in the country during treatment
- •are younger than 65 years of age
结局指标
主要结局
Change in chronic pain severity
时间窗: baseline, 8 weeks, 3 months
Measured by Brief Pain Inventory (BPI)
Change in depression
时间窗: baseline, 8 weeks, 3 months
Measured by Geriatric Depression Scale-30 (GDS-30)
Change in anxiety
时间窗: baseline, 8 weeks, 3 months
Measured by Generalized Anxiety Disorder Scale 7-Item (GAD-7)
Change in the impact of pain in several areas of life
时间窗: baseline, 8 weeks, 3 months
Measured by Pain Disability Index (PDI)
次要结局
- Change in tendency to amplify the threat value of constant pain(baseline, 8 weeks, 3 months)
- Treatment satisfaction(8 weeks)
- Change in acceptance of chronic pain(baseline, 8 weeks, 3 months)
- Change in beliefs about one's ability to perform every day tasks regardless of chronic pain(baseline, 8 weeks, 3 months)
- Change in fear of movement or re-injury(baseline, 8 weeks, 3 months)