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NCT05287087

My Symptoms - Feasibility Study

Completed NA Last updated 23 February 2024
What this trial tests

NA trial testing My Symptoms 1 (MySt-1) in Persistent Physical Symptoms in 40 participants. Completed in 30 June 2023.

Timeline
31 March 2022
Primary endpoint
30 September 2022
30 June 2023

Quick facts

Lead sponsorAarhus University Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingdouble
Primary purposeother
Enrollment40
Start date31 March 2022
Primary completion30 September 2022
Estimated completion30 June 2023
Sites1 location across Denmark

Drugs / interventions tested

Conditions studied

Sponsor

Aarhus University Hospital

Who can join

Adults 18 to 65, any sex, with Persistent Physical Symptoms. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The proposed project 'My Symptoms' is part of a large research programme: eHealth and GP-assisted self-help interventions for persistent physical symptoms (eASY). See www.minesymptomer.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. In order to improve health care for patients with PPS, the investigators have developed a web-based selfhelp programme for symptoms. As part of the intervention, this programme is prescribed by the patient's general practitioner (GP). 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 and how it affects GPs in routine care and patients in daily life. With this study, the investigators wish to take the first step towards a comprehensive and rigorous evaluation. Results from this feasibility study will both qualify a subsequent randomised controlled trial (RCT) in a larger pilot study and provide information for a potential national dissemination.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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