About this trial
This randomized controlled study will evaluate the effectiveness of real-time digital intelligence in the treatment of chronic pain. A total of 80 adult patients enrolled in a four-week multidisciplinary chronic pain programme will be randomly assigned to either standard treatment alone or standard treatment supported by a smartwatch and a mobile application for real-time monitoring of pain intensity, analgesic use, physical activity, and heart rate.
Both groups will complete validated questionnaires assessing pain intensity, disability, quality of life, sleep, anxiety, depression, and treatment satisfaction at baseline, two weeks, and four weeks. The intervention group will additionally record daily pain scores and medication use via a mobile application and wear a smartwatch for continuous activity and heart rate monitoring.
The study aims to determine whether real-time digital monitoring and physician availability improve clinical outcomes compared with standard multidisciplinary care alone.
Eligibility criteria
Qualifiers
Age 18-65 years Chronic low back pain significantly affecting disability and/or emotional distress
Active use of Croatian language
Signed informed consent
Disqualifiers
Age <18 or >65
Acute pain
Previous participation in multidisciplinary program
Pregnancy or cancer-related pain
Trial design
Treatments tested in this trial
- tandard Treatment + Digital Monitoring (Intervention Group)
- Standard Multidisciplinary Treatment (Control Group)