Evaluation of the Benefits of a Prehabilitation Program : Pilot Study
NCT ID: NCT02878551
Last Updated: 2021-03-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
50 participants
INTERVENTIONAL
2016-10-07
2017-06-23
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
SUPPORTIVE_CARE
NONE
Study Groups
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Prehabilitation program
Multimodal prehabilitation intervention composed of exercise, nutritional supplement and psychological well-being
Prehabilitation program
multimodal prehabilitation intervention composed of exercise, nutritional supplement and psychological well-being
Interventions
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Prehabilitation program
multimodal prehabilitation intervention composed of exercise, nutritional supplement and psychological well-being
Eligibility Criteria
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Inclusion Criteria
* Affiliated with a social security system
* Having indicated their non-opposition
* Must undergo a surgical intervention within a period of at least one month after the completion of the initial inclusion assessment and / or chemotherapy and / or radiotherapy
* Refusal of participation
* Pregnant or breastfeeding woman
* Inability to walk or initial physical assessment
* Patient under guardianship or curatorship
* Inability to complete questionnaires
Exclusion Criteria
* Lost
* Death before surgery or chemotherapy or radiotherapy
* Shortened preoperative preparation time (\<18 days)
18 Years
ALL
No
Sponsors
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Hopital Foch
OTHER
Responsible Party
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Principal Investigators
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Morgan Le Guen, MD
Role: PRINCIPAL_INVESTIGATOR
Hopital Foch
Locations
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Hopital Foch
Suresnes, , France
Countries
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Other Identifiers
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2016-A00981-50
Identifier Type: OTHER
Identifier Source: secondary_id
2016/29
Identifier Type: -
Identifier Source: org_study_id
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