search
Back to results

Evaluation of an Adapted Physical Activity Program in Patients With Unresectable Pancreatic Cancer

Primary Purpose

Unresectable Locally Advanced Cancer, Metastatic Pancreatic Cancer

Status
Active
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
without APA program
APA program
Sponsored by
GERCOR - Multidisciplinary Oncology Cooperative Group
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Unresectable Locally Advanced Cancer focused on measuring Unresectable, Pancreatic cancer, GERCOR, Adapted physical activity (APA), Quality of life, Fatigue

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Histologically proven non resectable pancreatic adenocarcinoma
  • Indication of palliative chemotherapy
  • Life expectancy ≥ 3 months
  • Eastern Cooperative oncology group (ECOG) - Performance status ≤2
  • Age ≥18 years old
  • At least one measurable lesion as assessed by CT-scan or MRI (Magnetic resonance Imaging)
  • Identified Accompanying partner Adapted Physical Activity (AAPA)
  • Signed and dated informed consent
  • Registration in a National Health Care System (CMU included for France)

Exclusion Criteria:

  • Previous Cerebrovascular accident or myocardial infarction <6months
  • Uncontrolled hypertension.
  • Severe cardiovascular or respiratory disease
  • Severe cognitive or psychiatric disorder
  • Severe motor and/or sensory neuropathy
  • Rheumatologic or orthopedic problem or bone lesions with a fracture risk
  • Others comorbidities contra-indicated physical exercises
  • Patient protected by the law - Guardianship and trusteeship

Sites / Locations

  • Polyclinique Bordeaux Nord Aquitaine
  • CHU Morvan
  • Hôpital Beaujon
  • Hôpital Henri Mondor
  • Centre Georges François Leclerc
  • CHD Vendée
  • Institut Hospitalier Franco-Britannique
  • Centre Léon Bérard
  • CH Saint Joseph Saint Luc
  • Hôpital Européen
  • CH Mont de Marsan
  • Centre Hospitalier de Belfort
  • Hôpital Cochin
  • Hôpital Saint Antoine
  • CHU Robert Debré
  • Hôpital FOCH
  • Institut de cancérologie de Lorraine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Standard care without APA program

Standard care with APA program

Arm Description

The control arm corresponds to usual care (without APA), including : Weekday hospital chemotherapy (every 7 or 14 days, depending on chemotherapy protocol) Evaluation by the oncologist at the usual rate Assessment every 8 weeks (TAP scan + CA-19.9) Nutritional, psychological and pain management as recommended, according to the usual schedule.

The experimental arm corresponds to usual care, combined with a 16-week APA program. The APA program consisted of personalized aerobic and resistance exercises, with a weekly remote supervision by an APA professional trainer, and unsupervised sessions with a family member or friend (APA partner).

Outcomes

Primary Outcome Measures

Health-related quality of life (HRQoL) at 16 weeks
HRQoL at week 16 according to the EORTC Core Quality of Life questionnaire (EORTC QLQ-C30) with three targeted dimensions: global health status, physical function and fatigue.

Secondary Outcome Measures

Time To deterioration (TTD)
Brief Pain Inventory Short form questionnaire
Patient depression scale - HADS questionnaire
Nutritional status evaluation
Nutritional Status will be measured by weigth, Body Mass Index, body composition, EVA ingests, caloric intake and protidic, albumin/prealbumin, inflammation markers (PNN and CRP)
Physical Activity evaluation - IPAQ questionnaire
Six minutes walk test, dyspnea scale, Borg scale, muscular pain, strength test with bands and compliance program
Number of Adverse events (AE) grade 3 -4
Progression free survival (PFS)
Overall Survival (OS)
Accompanying partner depression scale (HADS questionnaire)
General state - Performance status OMS
Fatigue scale (EVA fatigue)
MFI-20 and EORTC QLQ C-30 evaluation
medico-economic evaluation
visual analog scale for pain
analgesic consumption
anxiolytic / antidepressant consumption

Full Information

First Posted
July 2, 2014
Last Updated
September 26, 2023
Sponsor
GERCOR - Multidisciplinary Oncology Cooperative Group
search

1. Study Identification

Unique Protocol Identification Number
NCT02184663
Brief Title
Evaluation of an Adapted Physical Activity Program in Patients With Unresectable Pancreatic Cancer
Official Title
Multicenter, Randomized Study, Evaluation of Adapted Physical Activity Program in Patients With Unresectable, Locally Advanced or Metastatic Pancreatic Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
November 20, 2014 (Actual)
Primary Completion Date
April 21, 2022 (Actual)
Study Completion Date
December 30, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
GERCOR - Multidisciplinary Oncology Cooperative Group

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Adapted Physical Activity (APA) program may provide an opportunity to improve symptoms for patients with unresectable pancreatic cancer. Thereby, it is proposed to conduct an open trial to assess effects of the APA program in such population
Detailed Description
The benefit of Adapted Physical Activity (APA) has been demonstrated after cancer diagnosis in term of symptomatic improvement: reducing fatigue, pain and improving the quality of life, psychological and emotional state, and adherence to treatment. The aim of the study is to assess the effects of an APA program in pancreatic cancer population treated by usual chemotherapy. 200 randomized patients are required. The program is organized in 16 weeks. During the trial, assessments include: aerobic exercises, muscular strength, six-minute walk test, body composition (bioimpedance, L3 CT-scan), level of physical activity - International Physical Activity Questionnaire - (IPAQ questionnaire), fatigue - Multidimensional Fatigue Inventory - (MFI-20 questionnaire), quality of life - EORTC Quality of Life questionnaire C-30 - (EORTC QLQ-30 questionnaire), depression symptom - Hospital Anxiety and depression scale - (HADS questionnaire), pain (Brief Pain Inventory Short form), and nutritional evaluation (BMI, ingests EVA). Furthermore, relationships between insulin resistance, insulin secretion, Insulin like Growth Factor 1 (IGF-1) and pancreatic carcinogenesis exist. APA may improve the quality of life in decreasing insulin-resistance, insulin secretion and IGF-1.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Unresectable Locally Advanced Cancer, Metastatic Pancreatic Cancer
Keywords
Unresectable, Pancreatic cancer, GERCOR, Adapted physical activity (APA), Quality of life, Fatigue

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
313 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Standard care without APA program
Arm Type
Active Comparator
Arm Description
The control arm corresponds to usual care (without APA), including : Weekday hospital chemotherapy (every 7 or 14 days, depending on chemotherapy protocol) Evaluation by the oncologist at the usual rate Assessment every 8 weeks (TAP scan + CA-19.9) Nutritional, psychological and pain management as recommended, according to the usual schedule.
Arm Title
Standard care with APA program
Arm Type
Experimental
Arm Description
The experimental arm corresponds to usual care, combined with a 16-week APA program. The APA program consisted of personalized aerobic and resistance exercises, with a weekly remote supervision by an APA professional trainer, and unsupervised sessions with a family member or friend (APA partner).
Intervention Type
Other
Intervention Name(s)
without APA program
Intervention Description
Control Arm : chemotherapy alone
Intervention Type
Other
Intervention Name(s)
APA program
Intervention Description
Experimental Arm : chemotherapy + APA program during 16 weeks (aerobic and muscular strength exercises)
Primary Outcome Measure Information:
Title
Health-related quality of life (HRQoL) at 16 weeks
Description
HRQoL at week 16 according to the EORTC Core Quality of Life questionnaire (EORTC QLQ-C30) with three targeted dimensions: global health status, physical function and fatigue.
Time Frame
At 16 weeks
Secondary Outcome Measure Information:
Title
Time To deterioration (TTD)
Time Frame
Up to 24 months
Title
Brief Pain Inventory Short form questionnaire
Time Frame
Up to 24 months
Title
Patient depression scale - HADS questionnaire
Time Frame
Up to 24 months
Title
Nutritional status evaluation
Description
Nutritional Status will be measured by weigth, Body Mass Index, body composition, EVA ingests, caloric intake and protidic, albumin/prealbumin, inflammation markers (PNN and CRP)
Time Frame
up to 24 months
Title
Physical Activity evaluation - IPAQ questionnaire
Description
Six minutes walk test, dyspnea scale, Borg scale, muscular pain, strength test with bands and compliance program
Time Frame
up to 24 months
Title
Number of Adverse events (AE) grade 3 -4
Time Frame
up to 24 months
Title
Progression free survival (PFS)
Time Frame
2 years
Title
Overall Survival (OS)
Time Frame
2 years
Title
Accompanying partner depression scale (HADS questionnaire)
Time Frame
up to 24 months
Title
General state - Performance status OMS
Time Frame
up to 24 months
Title
Fatigue scale (EVA fatigue)
Time Frame
up to 24 months
Title
MFI-20 and EORTC QLQ C-30 evaluation
Time Frame
at 6, 12 et 24 months
Title
medico-economic evaluation
Time Frame
up to 24 months
Title
visual analog scale for pain
Time Frame
up to 24 months
Title
analgesic consumption
Time Frame
up to 24 months
Title
anxiolytic / antidepressant consumption
Time Frame
up to 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically proven non resectable pancreatic adenocarcinoma Indication of palliative chemotherapy Life expectancy ≥ 3 months Eastern Cooperative oncology group (ECOG) - Performance status ≤2 Age ≥18 years old At least one measurable lesion as assessed by CT-scan or MRI (Magnetic resonance Imaging) Identified Accompanying partner Adapted Physical Activity (AAPA) Signed and dated informed consent Registration in a National Health Care System (CMU included for France) Exclusion Criteria: Previous Cerebrovascular accident or myocardial infarction <6months Uncontrolled hypertension. Severe cardiovascular or respiratory disease Severe cognitive or psychiatric disorder Severe motor and/or sensory neuropathy Rheumatologic or orthopedic problem or bone lesions with a fracture risk Others comorbidities contra-indicated physical exercises Patient protected by the law - Guardianship and trusteeship
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Pascal Hammel, MD
Organizational Affiliation
Hôpital Beaujon
Official's Role
Principal Investigator
Facility Information:
Facility Name
Polyclinique Bordeaux Nord Aquitaine
City
Bordeaux
Country
France
Facility Name
CHU Morvan
City
Brest
Country
France
Facility Name
Hôpital Beaujon
City
Clichy
Country
France
Facility Name
Hôpital Henri Mondor
City
Creteil
Country
France
Facility Name
Centre Georges François Leclerc
City
Dijon
Country
France
Facility Name
CHD Vendée
City
La Roche Sur Yon
Country
France
Facility Name
Institut Hospitalier Franco-Britannique
City
Levallois Perret
Country
France
Facility Name
Centre Léon Bérard
City
Lyon
Country
France
Facility Name
CH Saint Joseph Saint Luc
City
Lyon
Country
France
Facility Name
Hôpital Européen
City
Marseille
Country
France
Facility Name
CH Mont de Marsan
City
Mont de Marsan
Country
France
Facility Name
Centre Hospitalier de Belfort
City
Montbéliard
Country
France
Facility Name
Hôpital Cochin
City
Paris
Country
France
Facility Name
Hôpital Saint Antoine
City
Paris
Country
France
Facility Name
CHU Robert Debré
City
Reims
Country
France
Facility Name
Hôpital FOCH
City
Suresnes
Country
France
Facility Name
Institut de cancérologie de Lorraine
City
Vandoeuvre Les Nancy
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
26458923
Citation
Neuzillet C, Vergnault M, Bonnetain F, Hammel P. Rationale and design of the Adapted Physical Activity in advanced Pancreatic Cancer patients (APACaP) GERCOR (Groupe Cooperateur Multidisciplinaire en Oncologie) trial: study protocol for a randomized controlled trial. Trials. 2015 Oct 12;16:454. doi: 10.1186/s13063-015-0983-8.
Results Reference
derived

Learn more about this trial

Evaluation of an Adapted Physical Activity Program in Patients With Unresectable Pancreatic Cancer

We'll reach out to this number within 24 hrs