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Tele-patient-reported Outcomes (telePRO) in Clinical Practice

University of Aarhus logo

University of Aarhus

Status

Completed

Conditions

Epilepsy

Treatments

Other: Open Access telePRO
Other: Standard telePRO

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT02673580
TELEPRO

Details and patient eligibility

About

The aim of this study is to compare quality of care and patient experiences in two outpatients follow-up activities: 1) Standard telePRO (fixed interval telePRO follow-up) and 2) Open Access telePRO (patient-initiated telePRO follow-up)

Full description

The traditional system of routine outpatient follow-up of chronic disease in secondary care may involve a waste of resources if patients are well. The use of patient-reported outcomes (PRO) could support more flexible, cost-saving follow-up activities. AmbuFlex is a PRO system used in outpatient follow-up in the Central Denmark Region. PRO questionnaires are sent to patients at fixed intervals. The clinicians use the PRO data to decide whether a patient needs a visit or not (standard telePRO). PRO may make patients become more involved in their own care pathway, which may improve their self-management. Better self-management may also be achieved by letting patients initiate contact. The aim of this study is to obtain data on the effects of patient-initiated follow-up (open access telePRO) on resource utilisation, quality of care, and the patient perspective.

Enrollment

593 patients

Sex

All

Ages

15+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Males and females from Age 15 years
  • Diagnosis of epilepsy
  • Referred to standard telePRO by a clinician
  • Access to internet (web-responders in standard telePRO)
  • Can speak and understand Danish

Exclusion criteria

  • Paper responders
  • Referred to telePRO proxy questionnaire

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

593 participants in 2 patient groups

Open Access telePRO
Other group
Description:
Intervention: In open access, contact to the outpatient clinic is initiated by the patient by filling in a PRO questionnaire.
Treatment:
Other: Open Access telePRO
Standard telePRO
Other group
Description:
No intervention: In standard telePRO, outpatient follow-up activity is determined by a clinician and patients receive a questionnaire at fixed intervals.
Treatment:
Other: Standard telePRO

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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