A Randomized Control Trial of Patient-initiated Hospital Follow-up for Patients With Psoriasis
- Conditions
- Psoriasis
- Interventions
- Procedure: Patient-initiated shared care
- Registration Number
- NCT02382081
- Lead Sponsor
- University Hospital, Gentofte, Copenhagen
- Brief Summary
The primary objective of this research protocol is to evaluate the health related quality of life and efficacy of patient-initiated hospital follow-up for patients with moderate to severe psoriasis.
- Detailed Description
Psoriasis is a chronic inflammatory skin disease affecting 1 to 3% of the European population. Treatment of moderate to severe psoriasis often requires lifetime routine reviews by hospital dermatologist. Patterns of hospital review vary, but most patients attend follow-up every 12-16 week by dermatologist. At routine reviews the patient disease is often quiet and little intervention or no intervention is required, and times were the patient need help the time is limited for in-depth consultation. Both patient and healthcare professional requested more time. In-depth consultation is important in the care of psoriasis, because moderate to severe psoriasis has a significant impact on quality of life and patient have an increased incidence of cardiovascular risk factors such as hypertension, overweight, hyperlipidemia and exposure to tobacco and alcohol. These comorbidities and the psychosocial burden must be addressed by clinicians to help patients to acquire or to maintain competencies that are required to live with a chronic disease.
Patient-initiated hospital follow-up for patients with moderate to severe psoriasis might reduce inappropriate follow-up appointments, improve rapid access to specialist care and release resource to further in-depth consultation. If the patient is empowered to initiate hospital review thus patient's individual needs dictate the content, duration and contact with clinicians. It is our goal that an individual needs-based patient involvement in the shape of patient-initiated hospital follow-up,will be perceived as a benefit of the patients who 1) meets a high safety in the patient's own provision of medical treatment, 2) increase the patient's knowledge of the lifestyle and prevention of comorbidities and 3) strengths patient's overall satisfaction with treatment.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 150
• Patients in stable systemic psoriasis treatment defined as having received treatment for more then 12 weeks without complication and being adherence to medication administration.
- Patients not able to give informed consent
- Patients not able to follow the program
- Patient with server psychiatric diseases
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Patient-initiated shared care Patient-initiated shared care Patient-initiated shared care hospital reviews in which there were one planed hospital review every year and if needed additional reviews initiated by the patient. Access to nurse-run telephone helpline with direct access to a contact nurse.
- Primary Outcome Measures
Name Time Method Dermatology life quality index (DLQI) 2 years Evaluation of quality of life
- Secondary Outcome Measures
Name Time Method SF36 - Short Form 36 (SF-36) 2 years Psoriasis Area and Severity Index (PASI 2 years Hospital Anxiety and Depression Scale (HADS) 2 years Body Image Scale (BIS) 2 years Self-developed patient safety scale 2 years Hospital visits 2 years Numbers of phone calls to the nurse-run telephone helpline 2 years Adherence to medicine treatment 2 years Charlson Comorbidity Index 2 years
Trial Locations
- Locations (1)
Gentofte Hospital, University of Copenhagen
🇩🇰Copenhagen, Denmark