Actively Recruiting

Phase Not Applicable
Age: 18Years - 67Years
All Genders
NCT05009459

eVISualisation of Physical Activity and Pain (eVIS) for Patients With Chronic Pain

Led by Dalarna University · Updated on 2025-08-28

280

Participants Needed

1

Research Sites

270 weeks

Total Duration

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Sponsors

D

Dalarna University

Lead Sponsor

S

Swedish Council for Working Life and Social Research

Collaborating Sponsor

AI-Summary

What this Trial Is About

Introduction: Living with chronic pain often involves negative consequences. Interdisciplinary Pain Rehabilitation Programs (IPRPs), a subset of Interdisciplinary Treatment (IDT) includes physical activity and exercise and is considered superior to single-treatment measures in patients with chronic pain. However, effects emerge sub-optimal and as many as 30% of patients deteriorate in some outcomes. A novel intervention, eVISualisation (eVIS) of physical activity and pain, has been systematically developed to facilitate patients in reaching and maintaining recommended individualized physical activity levels. The aim is to transparently report on methodology, outcome assessments, and processes for a registry-based randomized controlled trial (R-RCT) initiated as an internal pilot study. Methods and analysis: The R-RCT will recruit approximately 400 patients with chronic pain who are registered at primary and specialized IPRP units (n=15) in Sweden. Participants will be randomly allocated to either an IPRP + eVIS or the control group that will receive only IPRP treatment. eVIS entails objectively measured physical activity (steps) and patient-reported outcomes (pain intensity, affect on daily activities, pharmaceutical consumption) collected and visualized in the web application PATRON. Data from an initial 30 participants completing the study period (6 months) will be included in a pilot study designed to evaluate recruitment- and randomization processes, standardized effect size, sample size, characteristics of outcomes, follow-up rates of the R-RCT. Outcome variables will be extracted from PATRON and from six national registries. Multivariate statistics and repeated measures analyses will be performed. Quality Adjusted Life Years (QALYs) and Incremental Cost Effectiveness Ratio (ICER) will be calculated for cost effectiveness evaluation. Ethics/dissemination: The Swedish Ethics Review Board granted approval (Dnr 2021/02109). Results will be disseminated through peer-review journals.

CONDITIONS

Official Title

eVISualisation of Physical Activity and Pain (eVIS) for Patients With Chronic Pain

Who Can Participate

Age: 18Years - 67Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients have persistent or intermittent pain lasting 3 months or more
  • Pain greatly affects daily activities
  • Completed systematic assessment and non-pharmacological optimization
  • Screening for psychosocial risk factors and differential diagnosis completed
  • Aged between 18 and 67 years
  • Able to hear, see, and understand spoken and written Swedish
  • Have daily access to a computer, smartphone, or tablet
Not Eligible

You will not qualify if you...

  • Need to use a walking aid indoors
  • Have pain caused by systemic disease or malignancies

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Dalarna University

Falun, Sweden, SE-791 88

Actively Recruiting

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Research Team

V

Veronica Sjöberg, Phd

CONTACT

E

Elena Tseli, Dr

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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