Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT04706195

Early Accessible Person-centred Rehabilitation for Patients With Chronic Pain

Led by Göteborg University · Updated on 2023-07-05

220

Participants Needed

1

Research Sites

343 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of the research project EAPER-P is to evaluate PCC person-centred care (PCC) in the form of a combined eHealth and telephone support for patents with chronic pain. A developed PCC eHealth platform, together with person-centred telephone conversations, will be used as a tool to identify patients´ resources to enhance coping and living with their illness by means of a dialog and partnership with staff and relatives. PCC in the form of a combined eHealth and telephone support will not replace, but instead be used as add on treatment to usual care (guideline directed care). In addition, a process evaluation of the intervention will be performed in order to evaluate the mechanisms behind the intervention and evaluate which parts of the interventions the participants find useful.

CONDITIONS

Official Title

Early Accessible Person-centred Rehabilitation for Patients With Chronic Pain

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Men and women 18-65 years old.
  • Living with chronic, non-malignant, pain with any of the following diagnoses: M25, M54, M79 and R52
  • On sick leave (full or part time) from paid professional work.
  • Willing to participate
Not Eligible

You will not qualify if you...

  • Full time sick leave >24 months (part time sick leave >24 months can be included).
  • Severe impairment (cognitive or other) that prevents patient from using the eHealth support
  • No registered address
  • Not willing to participate
  • Any severe disease with an expected survival <12 months
  • Ongoing documented diagnosis of alcohol or drug abuse
  • Other severe disease that can interfere with follow-up or if the intervention is assessed as a burden
  • Patient participating in another conflicting randomized study
  • Patients not understanding spoken and written Swedish
  • Patient not having access to a device with internet access

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

Primary care

Gothenburg, Sweden

Actively Recruiting

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Research Team

S

Sara Wallström, PhD

CONTACT

L

Lilas Ali, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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