Actively Recruiting

Phase Not Applicable
Age: 20Years - 90Years
All Genders
ID05584410

Digitalization of the Care for Patients With Hip and Knee Osteoarthritis

Led by Vastra Gotaland Region · Updated on 2025-05-31

315

Participants Needed

1

Research Sites

156 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating three different care models for patients with hip and knee osteoarthritis to see if an app-based care model improves daily function better than a web-based model or standard care. The study also looks at patient outcomes like quality of life, pain confidence, physical activity, care use, cost-effectiveness, and environmental impact over short-term (three months) and long-term (one and three years) periods. It aims to understand patient experiences and adherence to the app and identify characteristics linked to meaningful improvements. The study includes three groups: the app-based care group, which involves at least one physical clinic visit and mostly app-delivered treatment with exercises, information, progress tracking, and messaging with a physiotherapist; the web-based group, which receives osteoarthritis information and exercises via a web platform with possible individualization and contact with a physiotherapist; and the standard care group, which attends group education sessions and supervised exercise visits at the clinic. Treatments generally last about three months. Participants will be followed with questionnaires and functional tests every six months up to three years. Researchers will measure function in daily living using the HOOS/KOOS score at one and three years, along with pain, symptoms, quality of life, physical activity, self-efficacy, cost-effectiveness, and environmental impact. Progress reports and contact from coordinators occur if symptoms worsen. The total participation can last up to three years after treatment starts.

CONDITIONS

Brief Title

Digitalization of Osteoarthritis Care

Who Can Participate

Age: 20Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Written consent to participate in the study
  • Referral to the orthopaedic clinic for primary hip or knee osteoarthritis
  • Positive attitude toward using digital tools
  • Access to a smartphone or tablet
  • Assessed not to need hip or knee surgery based on patient-reported outcome
Not Eligible

You will not qualify if you...

  • Secondary osteoarthritis due to osteonecrosis
  • Referral to a specific orthopaedic surgeon
  • Impaired mental ability, reluctance, or language difficulties preventing understanding of participation
  • Receiving treatment or having disability or illness that could affect treatment or study results

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person or digital) for assessment and consent

Treatment

Duration - Approximately 3 months

Participants receive one of three care models for hip or knee osteoarthritis: an app-based care model with individualized exercises and daily motivational notifications, a web-based care model with online exercises and support, or standard care including group information sessions and supervised rehabilitation. Treatment lasts approximately three months.

At least 1 physical visit with additional digital interactions depending on care model

Long-term Monitoring

Duration - Up to 3 years after treatment start

Participants are followed up every six months with questionnaires and function tests for up to three years to monitor symptoms, function, and progression. Reports are provided and further treatment is discussed if symptoms worsen.

Follow-up assessments every 6 months

Trial Site Locations

Total: 1 location

1

Sahlgrenska University Hospital

Gothenburg, Västra Götaland County, Sweden

Actively Recruiting

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Research Team

S

Susanne Beischer, PhD

M

Maziar Mohaddes, Assoc Prof

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

3

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