Recruiting NCT06201884
Efficacy of Adapted Physical Activity on a Walking Platform in Elderly Patients HOspitalized for Cancer Surgery
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Early rehabilitation through Adapted Physical Activity.
- Who it may be relevant to
- Registry conditions: Oncology, Elderly Patients, Surgery. Basic parameters: from 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The aim of this study was to evaluate the efficacy of daily use of a walking platform to improve recovery of preoperative walking speed at hospital discharge following oncological surgery in patients aged 65 or older.
Interventions
- Device Early rehabilitation through Adapted Physical Activity
From the day after surgery, 1 to 2 walking sessions with walking platform, lasting 6 to 30 minutes (min-max), will be proposed daily until the day of discharge.
Primary outcome measures
- To evaluate the efficacy of daily use of a walking platform to improve recovery of preoperative walking speed at hospital discharge following oncological surgery in patients aged 65 or older. [Time frame: at hospital discharge (approximately 15 to 30 days after surgery)]
Eligibility criteria
Inclusion criteria
- Men or women aged 65 or over
- Candidate for scheduled major oncological surgery and/or surgery with high morbidity
- Patient able to walk for 10 minutes on the walking platform at the time of the test
- Patient affiliated to a social security system
- Signature of informed consent prior to any specific study-related procedure
Exclusion criteria
- Patient with severe undernutrition (BMI<18, and/or weight loss >15% in 6 months or >10% in 1 month)
- Emergency surgery
- Physical contraindications preventing use of the platform
- Simultaneous participation in another clinical study that could compromise the conduct of this study
- Patients deprived of their liberty, under guardianship or subject to a legal protection measure, or unable to express their consent.
- Patient unable to undergo trial follow-up for geographical, social or psychopathological reasons.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
France · 2 centers
- Centre Francois Baclesse — Caen
- CHU CAEN — Caen
Identifiers
NCT: NCT06201884 · 2023-A01292-43