Track this trial free. DataLookout checks ClinicalTrials.gov daily and emails you which fields changed on NCT06290336 (status, enrollment, completion dates, endpoints, sites) when this record is updated. Free accounts track up to 5 trials.

Track this trial

Pre-Operative Exercise Therapy and Patient Education Before Total Knee Replacement

Study acronym: PROTEKT
StatusRecruiting
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Minor Re-verified, no change to tracked fieldsv4
  2. Notable Primary completion date: Dec 30, 2025 to Dec 30, 2027 Start date: Dec 20, 2023 to Feb 26, 2024 · Primary endpoints: 3 to 2 · Completion date: Dec 30, 2026 to Dec 30, 2027 · 1 morev3 Show 4 more changesShow less
    • Start date: Dec 20, 2023 to Feb 26, 2024
    • Primary endpoints: 3 to 2
    • Completion date: Dec 30, 2026 to Dec 30, 2027
    • Secondary endpoints: 12 to 13

    See this version in full on ClinicalTrials.gov ↗

  3. Notable Primary endpoints: 6 to 3 Eligibility criteria shortened, about 8 words · Secondary endpoints: 8 to 12v2 Show 2 more changesShow less
    • Eligibility criteria shortened, about 8 words
    • Secondary endpoints: 8 to 12

    See this version in full on ClinicalTrials.gov ↗

  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this multi-center randomized controlled trial is to investigate the effect of pre-operative exercise therapy and education for patients awaiting knee replacement surgery on subjective knee function, patient satisfaction and enablement compared to standard care. The main questions it aims to answer are: * Does pre-operative exercise therapy and education lead to better subjective knee function compared to standard care one year after surgery? * Does pre-operative exercise therapy and education lead to a higher level of patient satisfaction compared to standard care one year after surgery? * Does pre-operative exercise therapy and education lead to better patient enablement compared to standard care six weeks after surgery? * Does pre-operative exercise therapy and education lead to better objective knee function compared to standard care six weeks after surgery? Participants will be randomized stratified by age (≤ 67 years, \> 67 years) to either pre-operative supervised individualized exercise therapy combined with education two sessions/week (intervention group) or to standard care (control group). The intervention will be continuously ongoing for at least eight weeks from the point of decision for surgery until as close to the surgery as possible.
Trial Details
NCT Number NCT06290336
Lead Sponsor Linkoeping University
Collaborators: Region Östergötland, Region Jönköping County
Conditions Knee Osteoarthritis
Enrollment 110 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov