跳至主要内容
临床试验/NCT03952910
NCT03952910Unknown不适用

An Online Pain Education Program for Working Adults: a Pilot Randomized Controlled Trial With One-month Follow-up

The Hong Kong Polytechnic University1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2019年7月5日最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
60
试验地点
1
主要终点
Pain intensity and pain interference

研究概览

简要总结

Pain is popular among working population and it is a strong predictor of poor quality of life. In this study, an internet-delivered pain education program will be provided to working adults aims at helping patients equip with pain-related knowledge and useful skills and evaluate the effectiveness of the internet-delivered program. Participants will be recruited follow snowball sampling and will be randomly allocated to experimental group and control group by 1:1 ratio. The internet-delivered pain education will last for 4 weeks with one-month follow-up. Basic knowledge of pain, pharmacological and non-pharmacological treatment and related resources will be introduced in the program. Pain intensity, pain-related disability, anxiety, depression and self-efficacy will be measured in baseline post-treatment and at one-month follow-up. Acceptability and satisfaction to the program will also collected.

详细描述

Participants' eligibility will be accessed based on the following details:

  1. Inclusion criteria:

  2. . Age between 16 to 60;

  3. . Have a full-time job;

  4. . Resident of China;

  5. . Can read and understand Chinese;

  6. . History with non-cancer pain in past 6 months(Nicholas et al., 2013);

  7. . Pain score should be at least 2 when using Numeric Rating Scale, a 11-point numeric scale (Pieh et al., 2012);

  8. . Own a mobile phone and can access to mobile phone, computer and the internet.

  9. Exclusion criteria

  10. . Hospitalized patients;

  11. . Experiencing a drug addiction problem;

  12. . Further medical and surgical treatments or interventions is planned.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Age between 16 to 60;
  • Have a full-time job;
  • Resident of China;
  • Can read and understand Chinese;
  • History with non-cancer pain in past 6 months;
  • Pain score should be at least 2 when using Numeric Rating Scale, a 11-point numeric scale;
  • Own a mobile phone and can access to mobile phone, computer and the internet.

排除标准

  • Hospitalized patients;
  • Experiencing a drug addiction problem;
  • Further medical and surgical treatments or interventions is planned.

研究组 & 干预措施

Experimental group

Experimental

Online pain education program will be accessible by the intervention group

干预措施: Online pain education program (Other)

Control group

No Intervention

No intervention for the control group, only one-page simple material related to pain will be provided.

结局指标

主要结局

Pain intensity and pain interference

时间窗: Baseline, Week 4, one-month after intervention

Changes from baseline to Week 4 and one-month after the intervention in pain intensity and pain interference using Brief Pain Inventory

次要结局

  • Depression, Anxiety and Stress(Baseline, Week 4, one-month after intervention)
  • Pain self-efficacy(Baseline, Week 4, one-month after intervention)
  • Participant's Satisfaction and acceptability to the program(Week 4)

研究者

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

TSE Mun Yee Mimi

Associate professor

The Hong Kong Polytechnic University

研究点 (1)

Loading locations...

相似试验

An Online Pain Education Program for Working Adults | 临床试验