Connected Prehabilitation Program During Neo Adjuvant Chemotherapy

NCT ID: NCT04451369

Last Updated: 2021-02-10

Basic Information

• Recruitment Status: NOT_YET_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 136 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-05-31
• Study Completion Date: 2027-09-30

Brief Summary

NACT is a heavy oncologic treatment, which can impair functional capacity, nutritional and emotional status. These three impairments are often ignored and not taken into account in the pre-therapeutic evaluations but are correlated with postoperative morbidity and mortality after major surgery.

Recently, a prehabilitation before surgery, including physical, nutritional and psycho-social support, has been defined. From a literature review, the maximum oxygen uptake (VO2 max) seems to constitute a strong evaluation factor reflecting physical fitness, easily measured with a cardiopulmonary exercise test (CPET) at maximal effort.

Several studies have shown beneficial effects of trimodal prehabilitation programs on postoperative functional capacity, return to daily activities and pain relief.

Home-based program and connected devices may improve the feasibility and the compliance to this program.

The hypothesis of this study is that performing a connected supervised home-based and patient-tailored multimodal prehabilitation program from diagnosis to surgery (with or without ERAS program) during NACRT, for patients managed for ovarian cancer, will limit physical fitness alteration and will positively affect postoperative outcomes.

Our study consists in an early and multidimensional (combining nutritional, physical, emotional and medical support) prehabilitation program during NACT for patients with ovarian cancer, in order to limit physical alteration before surgical treatment, and therefore improve postoperative outcomes. It will include a home-based prehabilitation program, in order to allow care access to all eligible patients.

Detailed Description

The main objective will be to determine if a prehabilitation program during NACT, for patients treated for an advanced ovarian cancer will limit physical alteration before major abdomino-pelvic surgery, compared to a control group without prehabilitation program. The primary endpoint will be the comparison of the variation of VO2 max, between baseline and surgery, in the prehabilitation group vs control group: VO2 max will be measured with a cardiopulmonary exercise test (CPET) at maximal effort.

This prospective, multicentric randomized control trial will be conducted in 7 French comprehensive cancer Centers or University Hospital, in compliance with inclusion criteria. After an initial evaluation, patients will be randomized in two groups: Prehabilitation group (P group) and a Control group (C group).

For the P group, after baseline evaluation, we will be offering from diagnosis to surgery, during the NACT:

• A standardized, patient-tailored preoperative physical activity training program will be performed at home, from diagnosis to surgery. Supervision will be done with connected device (connected watches) and activity will be adapted,
• A nutritional care established in respect of the SFNEP-SFNCM guidelines. Nutritional support will be adapted by a dietician according to information transmitted daily (connected body fat weight scale),
• A psychological support with coping strategies.

For the C group: Patients with ovarian cancer will undergo NACT after baseline evaluation without prehabilitation program.

After NACT, for both groups, major abdomino-pelvic surgery will be done with or without ERAS pathway, according to the practice in each center.

Conditions

Ovarian Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: NONE

Study Groups

Control group

Group without prehabilitation program before surgery

Group Type: NO_INTERVENTION

No interventions assigned to this group

Prehabilitation group

Group will follows a prehabilitation program before surgery

Group Type: EXPERIMENTAL

Prehabilitation program

Intervention Type: OTHER

physical, nutritional and psycho-social supports before surgery

Interventions

Prehabilitation program

physical, nutritional and psycho-social supports before surgery

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Patient must have signed the written consent,

2. Age ≥ 18 years,

3. Patient with advanced ovarian cancer (AOC), FIGO Stage III - IV, undergoing surgery,

4. Patient with neo adjuvant chemotherapy (min 3 cycles, max 6 cycles),

5. Capability to perform a cardiopulmonary exercise test (CPET)

6. Patient affiliated to the national "Social Security" regimen or beneficiary of this regimen.

Exclusion Criteria

1. Patient with cognitive impairment,

2. Pregnancy,

3. Neoadjuvant treatment contraindications,

4. Physical adapted activity program contraindication,

5. No possibility to have access to connected devices or do not have a smartphone or a computer

6. Patient deprived of liberty or placed under the authority of a tutor,

7. Patient considered socially or psychologically unable to comply with the procedure and the required medical follow-up.

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Institut Paoli-Calmettes

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Central Contacts

Dominique GENRE, Dr

Role: CONTACT

drci.up@ipc.unicancer.fr

+33 4 91 22 37 78

References

Lambaudie E, Bannier/Braticevic C, Villaron/Goetgheluck C, Zemmour C, Boher JM, Ben Soussan P, Pakradouni J, Brun C, Lopez Almeida L, Marino P. TRAINING-Ovary 01 (connecTed pRehabiliAtIoN pelvIc caNcer surGery): multicenter randomized study comparing neoadjuvant chemotherapy for patients managed for ovarian cancer with or without a connected pre-habilitation program. Int J Gynecol Cancer. 2021 Jun;31(6):920-924. doi: 10.1136/ijgc-2020-002128. Epub 2020 Dec 1.

Reference Type: DERIVED

PMID: 33262113 (View on PubMed)

Other Identifiers

TRAINING-01-IPC 2018-039

Identifier Type: -

Identifier Source: org_study_id