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The project 'My Symptoms' is part of a large research programme: eHealth and GP-assisted self-help interventions for persistent physical symptoms (eASY). See www.mine-symptomer.dk.
The research programme is an ambitious and dedicated effort aiming at improvement of functioning and quality of life for individuals with persistent physical symptoms (PPS) and prevention of the development of chronic functional disorders and associated loss of working capacity and high use of health care. At present, access to specialized treatment of PPS is very limited and treatment capacity in general practice is restricted to brief consultations - often with poor opportunity to make a treatment plan for symptoms. As part of the research programme, the investigators have developed a web-based self-help programme for patient with PPS. This treatment programme is prescribed by the patient's general practitioner (GP). Only GPs who have participated in a short introduction course will be allowed for prescriptions.
The investigators have applied a high degree of user involvement (GPs and patients) in the development process but there is a need to evaluate how the new treatment programme is in fact adopted by GPs and patients.
With this study, the investigators wish to follow the national implementation using a before-after study design describing uptake and effects on GPs, patients and the health care system.
Full description
The project aims to evaluate the uptake and effects of the new self-help programme for PPS, the My Symptoms programme, prescribed and followed up by GPs.
Specific objectives are to:
Describe the use of the programme during routine care. This includes
Explore patient characteristics (appropriateness)
Describe patients' engagement with the programme with regard to time and frequency of access to modules and tools (fidelity)
Evaluate effects on patients' health, quality of life, functioning and satisfaction with care
Estimate effects on patients' use of health care services
Estimate effects on patients' work productivity
Estimate possible effects on health care costs provided the intervention is fully disseminated nationally.
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120 participants in 1 patient group
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Central trial contact
Lisbeth Frostholm, PhD; Marianne Rosendal, PhD
Data sourced from clinicaltrials.gov
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