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Efficacy of Pre-operative Prehabilitation in Patients With Limb Sarcoma

Study acronym: EPOP-SARCOMA
StatusRecruiting
PhasePhase 2
Started
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Record History

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  1. Primary and study completion dates: Nov 2027 to Nov 2029v11
  2. Re-verified, no change to tracked fieldsv10
  3. Primary and study completion dates: Nov 2025 to Nov 2027v9
  4. Re-verified, no change to tracked fieldsv8
  5. Start date changed from estimate of Sep 2022 to Sep 13, 2022v7
Show 5 earlier versionsHide 5 earlier versions
  1. Start date: May 2022 to Sep 2022
    • Primary and study completion dates: Jul 2025 to Nov 2025
    v6
  2. Primary and study completion dates: Sep 2023 to Jul 2025
    • Start date: Mar 2021 to May 2022
    • Secondary endpoints: details revised at 10 of 10 entries
    • Eligibility criteria expanded, about 4 words
    v5
  3. Start date: Jan 2021 to Mar 2021v4
  4. Start date: Dec 2020 to Jan 2021v3
  5. Trial status: Not Yet Recruiting to Recruiting
    • Start date: Sep 2020 to Dec 2020
    • Site details revised
    v2
  1. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
Institut Claudius Regaud
76 trials monitored
See 4 trials at risk
Sarcoma
1,026 trials monitored
See 67 trials at risk
This Phase II feasibility study, prospective, interventional, monocentric aiming to assess the interest of pre-operative rehabilitation in patients treated for bone or soft-tissue sarcoma of the limbs. This protocol will be based on the realisation of a surgical prehabilitation program adapted to the patient. This strategy will involve a team of several health professionals: rehabilitation doctor, physiotherapist, occupational therapist, specialised nurse, dietician and adapted physical activity teacher. The aim of an adapted surgical prehabilitation program is to improve the functional recovery of the treated limb and the patient's autonomy after surgery. Each patient will be followed until 24 months post surgery.
Trial Details
NCT Number NCT04515459
Lead Sponsor Institut Claudius Regaud
Conditions
(from sponsor)		 Sarcoma
Related terms Bone Neoplasms, Sarcoma
Enrollment 53 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov