NCT07875647

Brief Summary

This study aims to improve our understanding of how people with knee osteoarthritis think about, regulate, and adapt their physical activity while participating in Joint Academy's digital osteoarthritis programme for knee osteoarthritis. The study will investigate how understanding of the regulation of physical activity, psychological factors, and patterns of daily activity are related to participation in rehabilitation and changes in physical function over time. By gaining a better understanding of how people experience and manage physical activity in the context of knee osteoarthritis, we hope to improve the knee osteoarthritis programme and support rehabilitation that is better tailored to individual needs.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
500

participants targeted

Target at P75+ for all trials

Timeline
11mo left

Started Nov 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

October 9, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

October 15, 2026

Completed
17 days until next milestone

Study Start

First participant enrolled

November 1, 2026

Expected
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2027

29 days until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2027

Last Updated

October 15, 2026

Status Verified

October 1, 2026

Enrollment Period

10 months

First QC Date

October 9, 2026

Last Update Submit

October 9, 2026

Conditions

Outcome Measures

Primary Outcomes (2)

  • Patient Specific Functional Scale

    The Patient-Specific Functional Scale (PSFS) is a patient-reported outcome measure in which individuals identify activities that are important to them but are limited by their condition. Each activity is rated on a scale from 0 to 10, where 0 indicates inability to perform the activity and 10 indicates the ability to perform the activity at the pre-injury or pre-condition level. The PSFS is commonly used to monitor changes in function over time.

    From enrollment to the end of the treatment at 12 weeks

  • KOOS-12 Function subscale

    The functional subscale of the 12-items Knee injury and Osteoarthritis Outcome Score (KOOS-12) assesses knee-related physical function. Higher scores indicate better status. The baseline score will be used as the primary functional outcome in cross sectional analysis of activity patterns and psychological factors.

    From enrollment to the end of the treatment at 12 weeks.

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Patients with knee osteoarthritis enrolled in Joint Academy's rehabilitation programme in Sweden.

You may not qualify if:

  • Another serious primary condition is judged to be the main cause of the participant's symptoms (e.g., cancer, inflammatory joint disease, neurological disease, or persistent disability following hip fracture).
  • Physical exercise is contraindicated. Another health condition currently causes more severe symptoms than the knee condition for which treatment is sought (e.g., chronic widespread pain or fibromyalgia).
  • Age below 18 years. Inability to understand or communicate in Swedish or English.
  • In addition, individuals will be excluded from the research project if they:
  • Have cognitive or intellectual impairments that prevent the provision of informed consent.
  • Have disabilities or medical conditions that substantially limit independent performance of daily activities.
  • Have speech, visual, or hearing impairments that cannot be adequately compensated for by assistive devices and therefore prevent participation in data collection or, where applicable, qualitative interviews.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Joint Academy

Malmö, Sweden

Location

Related Publications (1)

  • Soderberg J, Holmstrom IK, Ehn M, Florin U, Von Heideken Wagert P. Ways of understanding the regulation of physical activity among persons with knee osteoarthritis in digital rehabilitation: a phenomenographic study. BMJ Open. 2026 Sep 23;16(9):e124247. doi: 10.1136/bmjopen-2026-124247.

    PMID: 42778241BACKGROUND

Related Links

MeSH Terms

Conditions

Osteoarthritis, Knee

Condition Hierarchy (Ancestors)

OsteoarthritisArthritisJoint DiseasesMusculoskeletal DiseasesRheumatic Diseases

Study Officials

  • Petra von Heideken Wågert, Prof.

    Department of Health Sciences, Innovation and Design, Mälardalen University, Västerås, Sweden

    STUDY CHAIR
  • Johan Söderberg, PhD Student

    Department of Health Sciences, Innovation and Design, Mälardalen University, Sweden

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Johan H Söderberg, PhD student

CONTACT

Petra von Heideken Wågert, Prof.

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

October 9, 2026

First Posted

October 15, 2026

Study Start (Estimated)

November 1, 2026

Primary Completion (Estimated)

September 1, 2027

Study Completion (Estimated)

September 30, 2027

Last Updated

October 15, 2026

Record last verified: 2026-10

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be made publicly available due to the sensitive nature of the health data and restrictions related to ethical approval, data protection requirements and data sharing agreements. Study material that do not contain individual-level participant data, such as the study protocol, statistical analysis plan and aggregated results may be made available where appropriate.

Locations