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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)

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