An eHealth program for managing persistent physical symptoms
My Symptoms: a Before-After Evaluation of an eHealth and GP Assisted Programme for Persistent Symptoms in Primary Care (eASY)
This study tests a web-based self-help program for people with ongoing physical symptoms to see if it can improve their health and quality of life.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 120 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Aarhus University Hospital Academic / other |
| Locations | 1 site (Aarhus) |
| Trial ID | NCT06163014 on ClinicalTrials.gov |
What this trial studies
The 'My Symptoms' project is part of a larger initiative aimed at improving the quality of life for individuals with persistent physical symptoms (PPS) through a web-based self-help program. This program is prescribed by general practitioners (GPs) who have undergone a specialized training course. The study will evaluate how well patients engage with the program, the effects on their health and quality of life, and the impact on healthcare utilization and work productivity. By assessing these factors, the project aims to provide insights into the effectiveness of eHealth interventions in primary care settings.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18-65 experiencing persistent physical symptoms who are registered with a participating GP.
Not a fit: Patients with acute symptoms, those requiring surgical or medicinal treatment, or individuals with severe comorbidities may not benefit from this program.
Why it matters
Potential benefit: If successful, this program could significantly enhance the management of persistent physical symptoms, leading to improved patient outcomes and reduced healthcare costs.
How similar studies have performed: Other studies have shown promise in using eHealth interventions for similar conditions, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 18-65 (target population for the programme) * The consultation targets symptom complaints * Listed with participating practice. Exclusion Criteria: * Symptoms are acute (not persistent) and there is no need for this intervention * Symptoms must primarily be treated by medicine or surgery * Patient severely affected by other disease * Not eligible due to language or cognitive problems
Where this trial is running
Aarhus
- Aarhus University Hospital — Aarhus, Denmark (Recruiting)
Study contacts
- Study coordinator: Marianne Rosendal, PhD
- Email: marose@rm.dk
- Phone: +4521476826
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.