Skip to main content
Clinical Trials/NCT02382081
NCT02382081
Completed
N/A

A Randomized Control Trial of Patient-initiated Hospital Follow-up for Patients With Psoriasis

University Hospital, Gentofte, Copenhagen1 site in 1 country150 target enrollmentMay 2, 2015
ConditionsPsoriasis

Overview

Phase
N/A
Intervention
Not specified
Conditions
Psoriasis
Sponsor
University Hospital, Gentofte, Copenhagen
Enrollment
150
Locations
1
Primary Endpoint
Dermatology life quality index (DLQI)
Status
Completed
Last Updated
8 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
May 2, 2015
End Date
February 17, 2018
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Gentofte, Copenhagen
Responsible Party
Principal Investigator
Principal Investigator

Lina R. Khoury

B.N., stud.cand.scient.sant

University Hospital, Gentofte, Copenhagen

Eligibility Criteria

Inclusion Criteria

  • Patients in stable systemic psoriasis treatment defined as having received treatment for more then 12 weeks without complication and being adherence to medication administration.

Exclusion Criteria

  • Patients not able to give informed consent
  • Patients not able to follow the program
  • Patient with server psychiatric diseases

Outcomes

Primary Outcomes

Dermatology life quality index (DLQI)

Time Frame: 2 years

Evaluation of quality of life

Secondary Outcomes

  • 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)

Study Sites (1)

Loading locations...

Similar Trials