Early Accessible Person-centred Rehabilitation for Patients With Chronic Pain
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 e
| Condition(s) | Chronic Pain |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | 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. |
| Who can participate | Inclusion Criteria: * 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 Exclusion Criteria: * 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 und |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Lead sponsor | Göteborg University |
| Locations | Gothenburg, Sweden |
| Start date | 2021-08-15 |
| NCT ID | NCT04706195 |
| Official listing | https://clinicaltrials.gov/study/NCT04706195 |