Evaluation of the Benefits of a Prehabilitation Program : Pilot Study

Not Applicable

Completed

• Conditions: Cancer; Surgery
• Interventions: Other: Prehabilitation program

• Registration Number: NCT02878551
• Lead Sponsor: Hopital Foch

Brief Summary

The process of enhancing functional capacity of the individual in anticipation of an upcoming stressor has been termed "prehabilitation". In the present pilot trial, the impact of a multimodal prehabilitation intervention composed of exercise, nutritional supplement and psychological well-being begun in the preoperative period will be evaluated.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2016-08-22
• Study First Submitted QC: 2016-08-24
• Study First Posted: 2016-08-25
• Study Start: 2016-10-07
• Primary Completion: 2017-06-23
• Study Completion: 2017-06-23
• Status Verified: 2021-03
• Last Update Submitted: 2021-03-05
• Last Update Posted: 2021-03-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• Patients over 18 years old
• 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

Non-inclusion criteria:

• 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:

• Cognitive disorders detected by the geriatric consultation
• Lost
• Death before surgery or chemotherapy or radiotherapy
• Shortened preoperative preparation time (<18 days)

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Exclusion Criteria

Not provided

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Prehabilitation program	Prehabilitation program	Multimodal prehabilitation intervention composed of exercise, nutritional supplement and psychological well-being

Primary Outcome Measures

Name	Time	Method
6 minutes walk test	7 months

Trial Locations

Locations (1)

Hopital Foch; 🇫🇷 Suresnes, France