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E-health Tool for Management of Chronic Pain Patients.

Evaluation of the Feasibility of an E-health Tool in the Follow-up and Characterization of Chronic Pain Patients.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03931694
Acronym
e-DOL
Enrollment
113
Registered
2019-04-30
Start date
2019-02-06
Completion date
2020-06-04
Last updated
2026-08-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pain

Keywords

Chronic pain, e-Health

Brief summary

Chronic pain affects approximately 20% of adults, 50% of the elderly population and over 1.5 billion people worldwide. Societal and economic issues are also crucial, as 60% of people with pain are less able or unable to work and 20% say they have lost their jobs because of pain. The overall cost of chronic pain is estimated at around 300 billion euros in the EU. Unfortunately, current treatments for chronic pain have limited effectiveness. Pain clinics, which support the most complex and refractory cases of chronic pain, as well as general practitioners and patients expect improvements, both in terms of therapeutic efficacy and organization of care. In order to allow the characterization and a personalized follow-up of chronic pain patients, Investigator has created e-DOL, a smartphone application for patients and a web platform for physicians. The purpose of this study is to evaluate the feasibility and clinical interest of an e-Health smartphone application for the characterization and follow-up of chronic pain patients..

Detailed description

This first clinical study will assess the acceptability of the tool both by caregivers at the 13 pain clinics and by a panel of 300 patients followed for 6 months. Based on the results of the study (end 2019), investigator will improve the tool in a version 2.0, which will then be evaluated in a large impact study, measuring the intrinsic therapeutic effect of eDOL.

Interventions

DEVICEe-DOL

e-health program (smartphone and web platform)

Sponsors

University Hospital, Clermont-Ferrand
Lead SponsorOTHER
Institut ANALGESIA
CollaboratorUNKNOWN

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* All patients with chronic pain * patients with and regular users of a smartphone * Non-opposition to participation in the study

Exclusion criteria

* Patient unable to understand or answer questionnaires

Design outcomes

Primary

MeasureTime frameDescription
Feasibility of the e-health toolOnce, up to 12 monthsFeasibility evaluated by analysis of user acceptability (custom questionnaire: ease of use, utility...)

Secondary

MeasureTime frameDescription
Typology of patient responsesWeekly, up to 6 monthsTemporal evolution of the pain intensity using 0-10 VAS
impact of the eHealth toolOnce, Up to 12 months.evaluation of the impact of the eHealth tool on current practices (clinician's opinion)

Countries

France

Contacts

PRINCIPAL_INVESTIGATORNoémie DELAGE

University Hospital, Clermont-Ferrand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 11, 2026