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Digital exercise program to test activity and sleep in spondyloarthritis

Tests a digital exercise program for adults with spondyloarthritis, a joint disease.

Plain-language title generated from the registry record
Registry title: Effects of a Digital Exercise Intervention on Sleep and Physical Activity in Patients With Spondyloarthritis

Key facts

Where
Bordeaux, Clermont-Ferrand, and Saint-Etienne, FranceSee the 3 sites

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 18 and 80 years old?

Source: NCT07034404, who can take part

Where in France

  • CHU de BordeauxBordeaux, FranceNo longer taking part
  • CHU Clermont-FerrandClermont-Ferrand, FranceNo longer taking part
  • CHU Saint-EtienneSaint-Etienne, FranceNo longer taking part

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University Hospital, Grenoble
Trial code
NCT07034404
Record updated
29 June 2025
Original description
The goal of this clinical trial is to assess whether a tailored digital Adapted Physical Activity (APA) program can improve physical activity levels and sleep quality in adults diagnosed with spondyloarthritis (SpA).Read full original descriptionShow less

Effects of a Digital Adapted Physical Activity Program on Physical Activity Levels and Sleep Quality in Patients With Spondyloarthritis: A Randomized, Controlled, Multicenter Study.

The goal of this clinical trial is to assess whether a tailored digital Adapted Physical Activity (APA) program can improve physical activity levels and sleep quality in adults diagnosed with spondyloarthritis (SpA).

The main questions it aims to answer are:

Does participation in a 6-month digital APA program increase average daily step count (measured with an activity tracker)? Does the program improve sleep quality (measured with the Pittsburgh Sleep Quality Index)? Researchers will compare participants receiving general physical activity advice (control group) to those following a structured digital APA program (intervention group) to see if the tailored digital support leads to better outcomes.

Participants will:

Complete baseline assessments including physical activity, sleep, pain, and quality of life measures.

Be randomly assigned to a control group or intervention group. For the intervention group, follow an individualized exercise program delivered through a virtual platform with support from an APA professional over 10 virtual sessions.

Wear a connected activity tracker (Withings) to monitor physical activity throughout the study.

Complete follow-up assessments at 6 and 12 months.

Inclusion: Adults aged 18 to 80; Followed in rheumatology for axial spondyloarthritis validating the ASAS or modified New York criteria at all stages of progression,; Physically inactive (less than 150 minutes of moderate-intensity leisure-time physical activity per week), assessed at inclusion using the Global Physical Activity Questionnaire (GPAQ); With stable treatment for 3 months; Signed informed consent; Membership of a social security scheme; Have access to a digital tool with an internet connection (tablet or smartphone).

Exclusion: Concurrent impairment by another osteoarticular pathology interfering with mobility of the spine or lower limbs,; Any contraindication to physical activity (unstable or poorly controlled coronary ischaemia, severe asthma or significant obstructive ventilatory disorder (FEV1/FVC < 70%, FEV1 < 60% predicted), musculoskeletal pathology interfering with physical activity, proliferative retinopathy, macroscopic proteinuria, poorly controlled hypertension, etc.); History of chest pain during physical activity; History of sudden death in a first-degree relative; History of thoracic irradiation; Central or peripheral neurological damage,; Hip, knee or ankle arthroplasty performed or scheduled within 18 months,; Patients who do more than 150 minutes of moderate-intensity vigorous physical activity per week as part of their leisure activities; Persons covered by articles L1121-5 to L1121-8 of the Public Health Code; Staff with a hierarchical link to the principal investigator; Non-inclusion criteria related to physical activity :; Body mass index >35 kg/m2.

ClinicalTrials.gov NCT07034404