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AsseSSing Impact in pSoriatic Treatment (ASSIST)

18 maj 2022 uppdaterad av: University of Oxford

How Does PsAID Implementation Affect Treatment Intensification and Patient Satisfaction in PsA

Psoriatic arthritis (PsA) is a form of inflammatory arthritis associated with the skin condition psoriasis. A variety of different treatments are used to try to control arthritis and skin psoriasis and management often involves trial and error to find the right medication for the right person. Very little is known about the decisions made to increase treatment in individual patients. Previous research in rheumatoid arthritis found that clinical measures of disease activity, patient reported outcomes and characteristics of the treating doctor all influenced the decision to change therapy in routine practice.

This investigators particularly want to establish whether routine use of the psoriatic arthritis impact of disease (PsAID-12) questionnaire in the clinic setting can enable a better understanding of the impact of PsA on each individual, improve physician-patient communication and lead to appropriate interventions. The PsAID-12 questionnaire is a relatively new European developed questionnaire measuring patient impact across 12 different domains in PsA.

This study will use routine implementation of the PsAID-12 questionnaire and see if this is related to treatment decisions and patient satisfaction. The investigators will also examine other factors that may influence treatment decisions including patient characteristics, physician characteristics, disease activity and quality of patient-physician interactions.

Studieöversikt

Status

Rekrytering

Betingelser

Intervention / Behandling

Detaljerad beskrivning

This is an observational, cross-sectional study addressing the factors influencing treatment decisions in patients with PsA. Participants will be treated as usual in their routine clinical practice, but decisions on treatment will be recorded - whether treatment is escalated, unchanged or reduced, and why.

The study will be conducted in 25 rheumatology centres in Europe (UK, France, Germany, Spain and Italy) with five centres in each country. Each participant will only attend for one single study visit which is likely to last around 30 minutes in total. This will be alongside the participant's routine clinic visit. The PsAID-12 questionnaire will be implemented on a tablet computer but the remaining outcomes will be collected on paper CRFs and transferred to a database for analysis.

Studietyp

Observationell

Inskrivning (Förväntat)

500

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studera Kontakt Backup

Studieorter

      • Clermont-Ferrand, Frankrike, 63000
      • Le Mans, Frankrike
      • Marseille, Frankrike
      • Paris, Frankrike, 75651
      • Toulouse, Frankrike
      • Barcelona, Spanien
        • Har inte rekryterat ännu
        • Hospital Clinic (Barcelona)
        • Kontakt:
      • Coruña, Spanien
      • Madrid, Spanien
        • Har inte rekryterat ännu
        • Hospital Universitario 12 de Octubre
        • Kontakt:
      • Oviedo, Spanien
        • Har inte rekryterat ännu
        • Hospital Universitario Central de Asturias
        • Kontakt:
      • Salamanca, Spanien
    • Greater Manchester
      • Manchester, Greater Manchester, Storbritannien, M13 9WL
        • Rekrytering
        • Manchester University NHS Foundation Trust
        • Kontakt:
    • Oxfordshire
      • Oxford, Oxfordshire, Storbritannien, OX39DU
        • Rekrytering
        • Oxford University Hospital NHS Foundation Trust
        • Kontakt:
    • Staffordshire
      • Stafford, Staffordshire, Storbritannien, ST16 3SR
        • Har inte rekryterat ännu
        • Midlands Partnership NHS Foundation Trust
        • Kontakt:
    • Wales
      • Cardiff, Wales, Storbritannien, CF14 4HH
    • Yorkshire
      • Bradford, Yorkshire, Storbritannien, BD9 6RJ
      • Bamberg, Tyskland
        • Rekrytering
        • Klinikum Bamburg
        • Kontakt:
          • Axel Hueber
      • Berlin, Tyskland
        • Rekrytering
        • Rheumatologische Schwerpunktpraxis
        • Kontakt:
          • Jan Brandt-Jurgens
      • Frankfurt, Tyskland
        • Rekrytering
        • Universitätsklinik Frankfurt
        • Kontakt:
          • Michaela Kohm
      • Herne, Tyskland
      • Planegg, Tyskland
        • Rekrytering
        • MVZ für Rheumatologie Dr. Martin Welcker GmbH
        • Kontakt:
          • Martin Welcker

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Testmetod

Icke-sannolikhetsprov

Studera befolkning

Adult participants with a diagnosis of PsA

Beskrivning

Inclusion Criteria:

  • Participant is willing and able to give informed consent for participation in the study and complete questionnaires in the local language.
  • Aged 18 years or above.
  • Diagnosed with PsA according to the ClASification of Psoriatic ARthritis (CASPAR) criteria and diagnosis confirmed by a rheumatologist (Taylor 2006).

Exclusion Criteria:

  • Patients who don't speak or read the local language
  • Patients who are not comfortable filling in an app-based questionnaire or paper CRF.
  • Patients with a new diagnosis of PsA at the current clinic visit

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

Kohorter och interventioner

Grupp / Kohort
Intervention / Behandling
Psoriatic arthritis
Psoriatic arthritis Impact of Disease questionnaires (PsAID) used within routine clinic consultation.
PsAID questionnaire

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Proportion of patients undergoing treatment escalation
Tidsram: During the consultation (cross sectional study so only one timepoint)
Treatment escalation definition includes increase in dose, frequency, change of route, new medication
During the consultation (cross sectional study so only one timepoint)

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Reduction of therapy
Tidsram: During the consultation (cross sectional study so only one timepoint)
Treatment reduction definition includes decrease in dose, frequency, change in route, stopping medication
During the consultation (cross sectional study so only one timepoint)
PsAID-12 scores
Tidsram: During the consultation (cross sectional study so only one timepoint)
PsA impact of disease score (scale 0-10 where higher score is worse)
During the consultation (cross sectional study so only one timepoint)
CollaboRATE score
Tidsram: During the consultation (cross sectional study so only one timepoint)
Patient satisfaction with consultation (scale 0-9 where higher score is better)
During the consultation (cross sectional study so only one timepoint)
Perceived efficacy on Patient-physician interaction score (PEPPI)
Tidsram: During the consultation (cross sectional study so only one timepoint)
Perceived efficacy in consultation (scale 5-25 where higher score is better)
During the consultation (cross sectional study so only one timepoint)
Physicians opinion of how much arthritis is driving treatment decision
Tidsram: During the consultation (cross sectional study so only one timepoint)
Visual Analogue Scale 0-10 (scale 0-10 where higher score is worse)
During the consultation (cross sectional study so only one timepoint)
Physicians opinion of how PsAID 12 influenced treatment decision
Tidsram: During the consultation (cross sectional study so only one timepoint)
Likert scale 1-5 (scale 0-5 where higher score is worse)
During the consultation (cross sectional study so only one timepoint)
Physicians opinion of how much enthesitis is driving treatment decision
Tidsram: During the consultation (cross sectional study so only one timepoint)
Visual Analogue Scale 0-10 (scale 0-10 where higher score is worse)
During the consultation (cross sectional study so only one timepoint)
Physicians opinion of how much psoriasis is driving treatment decision
Tidsram: During the consultation (cross sectional study so only one timepoint)
Visual Analogue Scale 0-10 (scale 0-10 where higher score is worse)
During the consultation (cross sectional study so only one timepoint)
Physicians opinion of how much systemic inflammation marker (CRP) is driving treatment decision
Tidsram: During the consultation (cross sectional study so only one timepoint)
Visual Analogue Scale 0-10 (scale 0-10 where higher score is worse)
During the consultation (cross sectional study so only one timepoint)
Physicians opinion of how much PROs are driving treatment decision
Tidsram: During the consultation (cross sectional study so only one timepoint)
Visual Analogue Scale 0-10 (scale 0-10 where higher score is worse)
During the consultation (cross sectional study so only one timepoint)

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Samarbetspartners

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

12 juli 2021

Primärt slutförande (Faktisk)

22 mars 2022

Avslutad studie (Förväntat)

31 december 2022

Studieregistreringsdatum

Först inskickad

24 november 2021

Först inskickad som uppfyllde QC-kriterierna

9 december 2021

Första postat (Faktisk)

28 december 2021

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

19 maj 2022

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

18 maj 2022

Senast verifierad

1 november 2021

Mer information

Termer relaterade till denna studie

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IPD-planbeskrivning

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