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Clinical Trials/NCT05103553
NCT05103553Not yet recruitingNot Applicable

Value Based Health Care in Systemic Sclerosis: What is the Optimal Follow-up for Patients With Systemic Sclerosis?

Leiden University Medical Center0 sites250 target enrollmentStarted: January 1, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
Enrollment
250
Primary Endpoint
Health care utilization Baseline

Study Overview

Brief Summary

Systemic sclerosis (SSc) is a complex multisystem rheumatic autoimmune disease. Currently, evidence based guidelines for frequency and intensity of follow-up of SSc patients are not available. Based on expert consensus annual extensive evaluation is recommended. To provide comprehensive multidisciplinary care integrated with evaluation of organ involvement and as such, reducing health care utilization while improving the quality of care for the patient, the "Leiden Combined Care in SSc (CCISS) pathway" was started in 2009. Data collected on disease progression in the patients that participate in this care pathway show that 50% of the patients have relatively mild disease, without any disease progression over time. Therefore there is a need for tailor made care in SSc patients in accordance to disease activity. To enable this, a prediction model was developed that can identify patients with low risk for disease progression.

Detailed Description

Objectives: To evaluate in SSc patients with low risk for disease progression 1) whether assessment in an outpatient clinic setting is an acceptable alternative for evaluation in the Care Pathway. Outcome parameters we will evaluate include 1) health care utilization, 2) patients' perception of the disease and delivery of care, 3) health-related quality of life and 4) disease progression. Health care utilization as primary outcome is defined as number of contacts with heath care providers during 12 months.

Study population: Patients with a clinical diagnosis of SSc that participated in the Combined Care in Systemic Sclerosis cohort from Leiden University Medical Center (LUMC), or in the comparable care pathway of the Haga hospital and Haaglanden Medical Center (HMC), and that have had at least two care pathway evaluations are eligible to participate in this study.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Participation in the prospective Haga, HMC or LUMC cohort
  • Clinical diagnosis of SSc
  • Age of ≥18 years
  • >= two evaluations in the Care Pathway
  • Low or intermediate risk for disease progression according to the prediction model
  • Written informed consent

Exclusion Criteria

  • Patients with SSc who are part of ongoing (randomized) trials
  • Patients who have had an autologous stem cell transplantation in the past five years
  • Patients with SSc who were categorized as high risk for disease progression according to the prediction model.

Outcomes

Primary Outcomes

Health care utilization Baseline

Time Frame: Baseline

Includes different health-care services: rheumatologist, other medical specialists, General Practioner (GP), health professionals, hospital admission, hospital based day-care. Number of contacts/visits within previous 6 months will be counted.

Health care utilization after 6 months

Time Frame: 6 months

Includes different health-care services: rheumatologist, other medical specialists, General Practioner (GP), health professionals, hospital admission, hospital based day-care. Number of contacts/visits within previous 6 months will be counted.

Health care utilization after 12 months

Time Frame: 12 months

Includes different health-care services: rheumatologist, other medical specialists, General Practioner (GP), health professionals, hospital admission, hospital based day-care. Number of contacts/visits within previous 6 months will be counted.

Health care utilization after 18 months

Time Frame: 18 months

Includes different health-care services: rheumatologist, other medical specialists, General Practioner (GP), health professionals, hospital admission, hospital based day-care. Number of contacts/visits within previous 6 months will be counted.

Health care utilization after 24 months

Time Frame: 24 months

Includes different health-care services: rheumatologist, other medical specialists, General Practioner (GP), health professionals, hospital admission, hospital based day-care. Number of contacts/visits within previous 6 months will be counted.

Secondary Outcomes

  • health-related quality of life using 36-item short form survey (SF-36)(Baseline, 6 months, 12 months, 18 months, 24 months)
  • health-related quality of life using EuroQol 5D (EQ5D)(Baseline, 6 months, 12 months, 18 months, 24 months)
  • Disease progression(Baseline, 6 months, 12 months, 18 months, 24 months)
  • Illness perception using the validated instrument Brief Illness Perception Questionnaire (BIPQ )(Baseline, 6 months, 12 months, 18 months, 24 months)

Investigators

Sponsor
Leiden University Medical Center
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Jeska K. de Vries-Bouwstra

Dr. / Principal Investigator

Leiden University Medical Center

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