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NCT06772896Completed

Evaluating the Effect of Questionnaire Context on the Reporting of Somatic Items Among People With Systemic Sclerosis

Evaluating the Effect of Questionnaire Context on the Reporting of Somatic Items in the 8-item Patient Health Questionnaire Among People With Systemic Sclerosis: A Scleroderma Patient-centered Intervention Network (SPIN) Study

Source: ClinicalTrials.gov · Last updated 9 Sept 2025

Brief summary (registry, in English)

There is concern that self-reported depression questionnaires that contain items assessing somatic symptoms may result in biased scores in people with a chronic disease due to symptoms that overlap with their physical disease. However, it has been shown in previous studies that biases associated with somatic items do not affect total depression scores. The reason for this is still unclear but could be associated with the context in which these items are presented. The goal of this experiment is to learn whether the way people with systemic sclerosis answer somatic items on a depression questionnaire is influenced by the fact that they are aware they are being assessed for depressive symptoms. The main question it aims to answer is: Do people with systemic sclerosis score somatic items differently when they are administered outside the context of a depression questionnaire? Participants will be randomly assigned to complete the 8-item Patient Health Questionnaire as part of their routine cohort assessments either with the items in their standard order or with somatic items presented first and separately from psychological items.

Status (registry)
Completed
Study type
Interventional
Enrollment
851 (actual)
First submitted
7 Jan 2025
Start date
17 Jan 2025
Primary completion date
17 Apr 2025
Lead sponsor
Lady Davis Institute
NCT number
NCT06772896

What you commit to

  • Study type: Interventional
  • Participants enrolled: 851
  • From 17 Jan 2025 to the primary completion date, 17 Apr 2025
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • None.

Who the study is looking for

  • SPIN Cohort patients must have a systemic sclerosis (SSc) diagnosis based on 2013 American College of Rheumatology/European League Against Rheumatism criteria confirmed by a SPIN physician, be ≥18 years old, be able to give informed consent, and be fluent in English, French or Spanish.
  • Participants must have access to a computer or tablet with internet access.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Jewish General Hospital
Coordinator of this site? Confirm its status
MontrealCanadaUnknown status
Lady Davis Institute for Medical Research
Coordinator of this site? Confirm its status
MontrealCanadaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.