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Impact of a Physical Activity Intervention With Motivational Support From Peers for Prostate Cancer Patients (ACTI-PAIR2)

Primary Purpose

Prostate Cancer

Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Acti-Pair program
Sponsored by
Centre Hospitalier Universitaire de Saint Etienne
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Prostate Cancer focused on measuring Physical activity, prostate cancer, interventional research

Eligibility Criteria

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

Inclusion Criteria: Patients: Age ≥ 18 years Diagnosed with prostate cancer for at least 1 year PA practice < 150 minutes per week (considered inactive according to WHO) Affiliated or entitled to a social security scheme Having received informed information about the study and having co-signed, with the investigator, a consent to participate in the study Exclusion Criteria: For patients: Undergoing treatment (except hormone therapy) Significant comorbidities contraindicating the practice of physical activity: associated cardiac pathologies, respiratory pathologies, disabling joint pathologies Deprived of liberty or under guardianship

Sites / Locations

  • CH Annonay
  • Activité Physique Adaptée - CDOS Savoie
  • CH Chambéry
  • Activité Physique Adaptée - DAHLIR 63
  • CHU Clermont-Ferrand - Oncologie
  • CHU Clermont-Ferrand - Urologie
  • Activité Physique Adaptée - CDOS Isère
  • CHU Grenoble - Urologie
  • Activité Physique Adaptée - DAHLIR 43
  • CH Le Puy en Velay
  • Activité Physique Adaptée - DAHLIR 69
  • CLB - Oncologie
  • CLB - Radiothérapie
  • HCL - CH Lyon Sud
  • Activité Physique Adaptée - CDOS Ardèche
  • CH Roanne
  • Activité Physique Adaptée - DAPAP 42
  • CHU Saint-Etienne - OncologieRecruiting
  • CHU Saint-Etienne - Radiothérapie
  • Hôpital Privé de la LoireRecruiting
  • Activité Physique Adaptée - CDOS Drôme
  • Hôpitaux Drôme Nord - Valence
  • Radiologie Drôme-Ardèche - Valence

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Acti-Pair program

Usual care

Arm Description

Motivational support by the peer (a patient with the same pathology who meets the WHO recommendations for physical activity), who will provide motivational follow-up The implementation of a personalized and realistic physical activity project for the patient via the physical activity support systems (sport health centers) Support from health professionals (GP) via the prescription of physical activity and from adapted physical activity (APA) professionals

The control group will be made up of patients followed up for prostate cancer and benefiting from usual care which consists of giving advice and recommendations for physical activity in consultation, aiming to make patients more active in their daily lives (=usual practice, physical activity to be carried out independently, at home).

Outcomes

Primary Outcome Measures

Objective measurement of physical activity (in MET-hr/week, Metabolic Equivalent of Task (MET), measures the intensity of physical activity)
via actimetry (Actigraph GT9x, Pensacola, Florida, USA) 12 months (+/- 1 month) after the patient's inclusion in the Acti-Pair program

Secondary Outcome Measures

Objective measurement of physical activity (in MET-hr/week, Metabolic Equivalent of Task (MET), measures intensity of physical activity)
via actimetry (Actigraph GT9x, Pensacola, Florida, USA) (at 3 and 6 months).
Objective measure of physical inactivity (in h/d)
via actimetry (Actigraph GT9x, Pensacola, Florida, USA)
Subjective measurement of physical activity (in Metabolic equivalent of task-h/week) and sedentary time (h/d)
Via the e-Adult Physical Activity Questionnaire (e-APAQ, EA SNA-EPIS, University of Jean Monnet, Saint-Etienne, France) e-Adult Physical Activity Questionnaire (e-APAQ) assesses the 5 categories of physical activity (work, travel, daily life, leisure and sport) and daily life, leisure and sport). The minimum value is 1 and the maximum value is 300. More the physical activity score is high, more the patient is active. This questionnaire authenticates the periods of sedentarity (at work, during travel and daily life, leisure and sport). The minimum value is 1 and the maximum value is 24. More the sedentarity score is high, more the patient is sedentary.
Measurement of physical capacity: walking distance (meters)
via the 6-minute walk test (6MWT).
Measurement of muscle strength: biceps muscle strength (kg)
via the handgrip (JAMAR Hand Dynamometer, Nottingham, UK).
Level of fatigue assessed by measuring heart rate variability (SDNN and RMSSD in ms)
via heart rate monitor connected to an actimeter (Actigraph GT3x, Pensacola, Florida, USA) for 24 hours
Level of fatigue
via the FACIT-F questionnaire (Functional Assessment of Chronic Illness Therapy - Fatigue Scale). This questionnaire asseses fatigue and it impacts. The score range is 0 to 160. More the score is higher, more the fatigue is high.
Health-related quality of life
via the EuroQol-5D questionnaire (EQ-5D-5L). The score range is -0.148 to 0.949. Mre the score is high, more the quality of life is good.
Adoption of Acti-Pair program by physicians
Number of physicians including patients
Adoption of Acti-Pair program by peers
Number of peers recruited
Adoption of Acti-Pair program by Adapted Physical Activity (APA) professionals
Number of patients followed by APA professionals
Time dedicated by peers, Adapted Physical Activity (APA) professionals and health professionals to the Acti-Pair program
Number of hours spend to follow-up patient specifically for the Acti-Pair program by peers, Adapted Physical Activity (APA) professionals and health professionals
Assessment of the context:factors favoring and hindering implementation, achievement, adaptation and sustainability of the programme ; compliance with the programme ; social representations
Semi-structured interviews
Percentage of adherence to the intervention
via the number of patients continuing the programme 12 months after initiation
Motivation to engage in physical activity for patients and peers
via the behavioural regulation in exercise questionnaire (BREQ-2). This questionnaire consists of 19 items includes 6 sub-scores of motivations : introjected regulation (3 items), external regulation (4 items), intrinsic regulation (4 items), integrated regulation, amotivation (4 items) and identified regulation (4 items) on a scale from 1 (Not at all true for me) to 5 (Absolutely true for me).
Alliance between the patient and the peer
via the Working Alliance Inventory - short version (WAI-SR). This questionnaire measures three dimensions: bonding (development of a positive interpersonal attachment between the patient and the peer including mutual trust and respect), tasks (each partner's perception of the appropriateness and effectiveness of the care tasks, as well as tasks, as well as shared responsibility for their execution) and goals (understanding, validation and acceptance by both partners of the objectives of change in physical activity management). Patients rate items on a 5-point Likert scale anchored at each end with 'rarely or never' (1) and 'always' (5). The Goal, Task and Bond domains each have scores ranging from 5 to 20. Higher scores indicate a better therapeutic alliance.
Patients, peers and professionals satisfaction
Via a satisfaction questionnaire constructed for the Acti-Pair programme. The proposed responses are a likert scale ranging from Strongly Agree to Strongly Disagree. Each item will be described with a percentage of Likert scale for each response. More participants will fill out they have been strongly agree, more they will be satisfied.This questionnaire does not have a score.
Cost per quality adjusted life year (QALY) gained through the intervention (quality adjusted life year)
Quality of life data will be collected (e.g. quality of life using the EQ-5D-5L questionnaire, Appendix 3), transformed into utilities to calculate quality adjusted life year (QALY), and the number of patients continuing physical activity at 12 months. Cost data will be collected throughout the study, in each of the 8 departments involved. The analysis will be carried out from the payer's (health insurance) perspective. The time horizon will be that of the study (12 months), and therefore in accordance with French guidelines (HAS), no discount rate will be applied
Cost per patient continuing physical activity at 12 months through the intervention
The costs will include : - direct medical costs : health professionals consultations, peer-to-peer, patient sessions with APA professionals - indirect costs of implementing the intervention: training, facility rental operating costs, investment in small equipment

Full Information

First Posted
January 26, 2023
Last Updated
June 13, 2023
Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Collaborators
Sport Health Center of Auvergne-Rhône Alpes, INSERM, SAINBIOSE U1059, INSERM, CIC1408, INSERM ECEVE 1123, Ministry of Health, France
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1. Study Identification

Unique Protocol Identification Number
NCT05739565
Brief Title
Impact of a Physical Activity Intervention With Motivational Support From Peers for Prostate Cancer Patients
Acronym
ACTI-PAIR2
Official Title
Title Impact of a Physical Activity Intervention With Motivational Support From Peers for Prostate Cancer Patients - ACTI-PAIR 2 Multicenter, Randomized Stepped-wedge Study
Study Type
Interventional

2. Study Status

Record Verification Date
June 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 25, 2023 (Actual)
Primary Completion Date
July 31, 2025 (Anticipated)
Study Completion Date
July 31, 2027 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Centre Hospitalier Universitaire de Saint Etienne
Collaborators
Sport Health Center of Auvergne-Rhône Alpes, INSERM, SAINBIOSE U1059, INSERM, CIC1408, INSERM ECEVE 1123, Ministry of Health, France

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Despite the recognized benefits of physical activity in tertiary prevention, 60-70% of prostate cancer patients are insufficiently active. Yet 150 minutes of brisk walking per week (new WHO recommendations) is associated with a 29% reduction in cancer mortality and a 57% reduction in recurrence. Increasing patients' adherence to regular physical activity appears to be a new challenge for personalized cancer care. Personalized physical activity programmes (1) at home, (2) supported by health professionals, or (3) by peers have shown the effectiveness of regular physical activity. However, these interventions last less than 6 months and do not allow for long-term sustainability of physical activity. This study proposes to combine 3 interventions, which aim to initiate and maintain regular physical activity in prostate cancer patients: 1-The realization of a personalized and realistic physical activity project via physical activity support devices (sport health centers) 2-Coaching by a peer (a patient with the same disease who has reached the WHO recommendations for physical activity), who will provide motivational follow-up 3-Support by health professionals (attending physician) through the prescription of physical activity. The feasibility of ACTI-PAIR program has been demonstrated, the investigators now wish to evaluate it effectiveness.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Physical activity, prostate cancer, interventional research

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
850 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Acti-Pair program
Arm Type
Experimental
Arm Description
Motivational support by the peer (a patient with the same pathology who meets the WHO recommendations for physical activity), who will provide motivational follow-up The implementation of a personalized and realistic physical activity project for the patient via the physical activity support systems (sport health centers) Support from health professionals (GP) via the prescription of physical activity and from adapted physical activity (APA) professionals
Arm Title
Usual care
Arm Type
No Intervention
Arm Description
The control group will be made up of patients followed up for prostate cancer and benefiting from usual care which consists of giving advice and recommendations for physical activity in consultation, aiming to make patients more active in their daily lives (=usual practice, physical activity to be carried out independently, at home).
Intervention Type
Behavioral
Intervention Name(s)
Acti-Pair program
Intervention Description
Motivational support by the peer (a patient with the same pathology who meets the WHO recommendations for physical activity), who will provide motivational follow-up The implementation of a personalized and realistic physical activity project for the patient via the physical activity support systems (sport health centers) Support from health professionals (GP) via the prescription of physical activity and from adapted physical activity (APA) professionals
Primary Outcome Measure Information:
Title
Objective measurement of physical activity (in MET-hr/week, Metabolic Equivalent of Task (MET), measures the intensity of physical activity)
Description
via actimetry (Actigraph GT9x, Pensacola, Florida, USA) 12 months (+/- 1 month) after the patient's inclusion in the Acti-Pair program
Time Frame
Month: 12
Secondary Outcome Measure Information:
Title
Objective measurement of physical activity (in MET-hr/week, Metabolic Equivalent of Task (MET), measures intensity of physical activity)
Description
via actimetry (Actigraph GT9x, Pensacola, Florida, USA) (at 3 and 6 months).
Time Frame
Inclusion, 3, 6 and 12 months
Title
Objective measure of physical inactivity (in h/d)
Description
via actimetry (Actigraph GT9x, Pensacola, Florida, USA)
Time Frame
Inclusion, 3, 6 and 12 months
Title
Subjective measurement of physical activity (in Metabolic equivalent of task-h/week) and sedentary time (h/d)
Description
Via the e-Adult Physical Activity Questionnaire (e-APAQ, EA SNA-EPIS, University of Jean Monnet, Saint-Etienne, France) e-Adult Physical Activity Questionnaire (e-APAQ) assesses the 5 categories of physical activity (work, travel, daily life, leisure and sport) and daily life, leisure and sport). The minimum value is 1 and the maximum value is 300. More the physical activity score is high, more the patient is active. This questionnaire authenticates the periods of sedentarity (at work, during travel and daily life, leisure and sport). The minimum value is 1 and the maximum value is 24. More the sedentarity score is high, more the patient is sedentary.
Time Frame
Inclusion, 3, 6 and 12 months
Title
Measurement of physical capacity: walking distance (meters)
Description
via the 6-minute walk test (6MWT).
Time Frame
Inclusion, 3, 6 and 12 months
Title
Measurement of muscle strength: biceps muscle strength (kg)
Description
via the handgrip (JAMAR Hand Dynamometer, Nottingham, UK).
Time Frame
Inclusion, 3, 6 and 12 months
Title
Level of fatigue assessed by measuring heart rate variability (SDNN and RMSSD in ms)
Description
via heart rate monitor connected to an actimeter (Actigraph GT3x, Pensacola, Florida, USA) for 24 hours
Time Frame
Inclusion, 3, 6 and 12 months
Title
Level of fatigue
Description
via the FACIT-F questionnaire (Functional Assessment of Chronic Illness Therapy - Fatigue Scale). This questionnaire asseses fatigue and it impacts. The score range is 0 to 160. More the score is higher, more the fatigue is high.
Time Frame
Inclusion, 3, 6 and 12 months
Title
Health-related quality of life
Description
via the EuroQol-5D questionnaire (EQ-5D-5L). The score range is -0.148 to 0.949. Mre the score is high, more the quality of life is good.
Time Frame
Inclusion, 3, 6 and 12 months
Title
Adoption of Acti-Pair program by physicians
Description
Number of physicians including patients
Time Frame
through end of inclusion, an average of 30 months
Title
Adoption of Acti-Pair program by peers
Description
Number of peers recruited
Time Frame
through end of inclusion, an average of 30 months
Title
Adoption of Acti-Pair program by Adapted Physical Activity (APA) professionals
Description
Number of patients followed by APA professionals
Time Frame
through study completion, an average of 42 Months
Title
Time dedicated by peers, Adapted Physical Activity (APA) professionals and health professionals to the Acti-Pair program
Description
Number of hours spend to follow-up patient specifically for the Acti-Pair program by peers, Adapted Physical Activity (APA) professionals and health professionals
Time Frame
through study completion, an average of 42 Months
Title
Assessment of the context:factors favoring and hindering implementation, achievement, adaptation and sustainability of the programme ; compliance with the programme ; social representations
Description
Semi-structured interviews
Time Frame
Before and after the implementation of the intervention
Title
Percentage of adherence to the intervention
Description
via the number of patients continuing the programme 12 months after initiation
Time Frame
12 months
Title
Motivation to engage in physical activity for patients and peers
Description
via the behavioural regulation in exercise questionnaire (BREQ-2). This questionnaire consists of 19 items includes 6 sub-scores of motivations : introjected regulation (3 items), external regulation (4 items), intrinsic regulation (4 items), integrated regulation, amotivation (4 items) and identified regulation (4 items) on a scale from 1 (Not at all true for me) to 5 (Absolutely true for me).
Time Frame
Inclusion, 3, 6 and 12 months
Title
Alliance between the patient and the peer
Description
via the Working Alliance Inventory - short version (WAI-SR). This questionnaire measures three dimensions: bonding (development of a positive interpersonal attachment between the patient and the peer including mutual trust and respect), tasks (each partner's perception of the appropriateness and effectiveness of the care tasks, as well as tasks, as well as shared responsibility for their execution) and goals (understanding, validation and acceptance by both partners of the objectives of change in physical activity management). Patients rate items on a 5-point Likert scale anchored at each end with 'rarely or never' (1) and 'always' (5). The Goal, Task and Bond domains each have scores ranging from 5 to 20. Higher scores indicate a better therapeutic alliance.
Time Frame
12 months
Title
Patients, peers and professionals satisfaction
Description
Via a satisfaction questionnaire constructed for the Acti-Pair programme. The proposed responses are a likert scale ranging from Strongly Agree to Strongly Disagree. Each item will be described with a percentage of Likert scale for each response. More participants will fill out they have been strongly agree, more they will be satisfied.This questionnaire does not have a score.
Time Frame
12 months
Title
Cost per quality adjusted life year (QALY) gained through the intervention (quality adjusted life year)
Description
Quality of life data will be collected (e.g. quality of life using the EQ-5D-5L questionnaire, Appendix 3), transformed into utilities to calculate quality adjusted life year (QALY), and the number of patients continuing physical activity at 12 months. Cost data will be collected throughout the study, in each of the 8 departments involved. The analysis will be carried out from the payer's (health insurance) perspective. The time horizon will be that of the study (12 months), and therefore in accordance with French guidelines (HAS), no discount rate will be applied
Time Frame
12 months
Title
Cost per patient continuing physical activity at 12 months through the intervention
Description
The costs will include : - direct medical costs : health professionals consultations, peer-to-peer, patient sessions with APA professionals - indirect costs of implementing the intervention: training, facility rental operating costs, investment in small equipment
Time Frame
12 months

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients: Age ≥ 18 years Diagnosed with prostate cancer for at least 1 year PA practice < 150 minutes per week (considered inactive according to WHO) Affiliated or entitled to a social security scheme Having received informed information about the study and having co-signed, with the investigator, a consent to participate in the study Exclusion Criteria: For patients: Undergoing treatment (except hormone therapy) Significant comorbidities contraindicating the practice of physical activity: associated cardiac pathologies, respiratory pathologies, disabling joint pathologies Deprived of liberty or under guardianship
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
HUPIN DAVID, MD
Phone
(0)477828413
Ext
+33
Email
David.Hupin@chu-st-etienne.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Amandine BAUDOT, CRA
Phone
(0)477829450
Ext
+33
Email
amandine.baudot@chu-st-etienne.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
David HUPIN, MD PhD
Organizational Affiliation
CHU de Saint-Etienne
Official's Role
Principal Investigator
Facility Information:
Facility Name
CH Annonay
City
Annonay
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Amine MESSAOUD, MD
Facility Name
Activité Physique Adaptée - CDOS Savoie
City
Chambéry
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fabrice DESCOMBES, MD
Facility Name
CH Chambéry
City
Chambéry
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Guillaume MORICEAU, MD
Facility Name
Activité Physique Adaptée - DAHLIR 63
City
Clermont-Ferrand
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joris MARTIN, MD
Facility Name
CHU Clermont-Ferrand - Oncologie
City
Clermont-Ferrand
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Florian CERUTI, MD
First Name & Middle Initial & Last Name & Degree
Florian CERUTI, MD
Facility Name
CHU Clermont-Ferrand - Urologie
City
Clermont-Ferrand
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Laurent GUY, MD
First Name & Middle Initial & Last Name & Degree
Laurent GUY, MD
Facility Name
Activité Physique Adaptée - CDOS Isère
City
Grenoble
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Manon GIRARD, MD
First Name & Middle Initial & Last Name & Degree
Manon GIRARD, MD
Facility Name
CHU Grenoble - Urologie
City
Grenoble
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean-Luc DESCOTES, MD
First Name & Middle Initial & Last Name & Degree
Jean-Luc DESCOTES, MD
Facility Name
Activité Physique Adaptée - DAHLIR 43
City
Le Puy-en-Velay
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anaïs CHARRA, MD
First Name & Middle Initial & Last Name & Degree
Anaïs CHARRA, MD
Facility Name
CH Le Puy en Velay
City
Le Puy-en-Velay
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Corinne BRUCHET, MD
First Name & Middle Initial & Last Name & Degree
Corinne BRUCHET, MD
Facility Name
Activité Physique Adaptée - DAHLIR 69
City
Lyon
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Julie Julie, MD
First Name & Middle Initial & Last Name & Degree
Julie Julie, MD
Facility Name
CLB - Oncologie
City
Lyon
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Cécile LAUDE, MD
First Name & Middle Initial & Last Name & Degree
Cécile LAUDE, MD
Facility Name
CLB - Radiothérapie
City
Lyon
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sofiane HANAYA, MD
First Name & Middle Initial & Last Name & Degree
Sofiane HANAYA, MD
Facility Name
HCL - CH Lyon Sud
City
Lyon
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alain RUFFION, MD
First Name & Middle Initial & Last Name & Degree
Alain RUFFION, MD
Facility Name
Activité Physique Adaptée - CDOS Ardèche
City
Privas
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jonathan BAZARD, MD
Facility Name
CH Roanne
City
Roanne
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lionel VINCENT, MD
First Name & Middle Initial & Last Name & Degree
Lionel VINCENT, MD
Facility Name
Activité Physique Adaptée - DAPAP 42
City
Saint-Étienne
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maël GARROS, MD
First Name & Middle Initial & Last Name & Degree
Maël GARROS, MD
Facility Name
CHU Saint-Etienne - Oncologie
City
Saint-Étienne
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Pierre CORNILLON, MD
First Name & Middle Initial & Last Name & Degree
Pierre CORNILLON, MD
Facility Name
CHU Saint-Etienne - Radiothérapie
City
Saint-Étienne
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anne-Laure BAREILLE, MD
First Name & Middle Initial & Last Name & Degree
Anne-Laure BAREILLE, MD
Facility Name
Hôpital Privé de la Loire
City
Saint-Étienne
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Stéphane LORIN, MD
First Name & Middle Initial & Last Name & Degree
Stéphane LORIN, MD
Facility Name
Activité Physique Adaptée - CDOS Drôme
City
Valence
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aline CARLIER, MD
Facility Name
Hôpitaux Drôme Nord - Valence
City
Valence
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thomas POLGUER, MD
Facility Name
Radiologie Drôme-Ardèche - Valence
City
Valence
Country
France
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean-Baptiste GUY, MD

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
25527697
Citation
Bonn SE, Sjolander A, Lagerros YT, Wiklund F, Stattin P, Holmberg E, Gronberg H, Balter K. Physical activity and survival among men diagnosed with prostate cancer. Cancer Epidemiol Biomarkers Prev. 2015 Jan;24(1):57-64. doi: 10.1158/1055-9965.EPI-14-0707. Epub 2014 Dec 19.
Results Reference
background
PubMed Identifier
21610110
Citation
Richman EL, Kenfield SA, Stampfer MJ, Paciorek A, Carroll PR, Chan JM. Physical activity after diagnosis and risk of prostate cancer progression: data from the cancer of the prostate strategic urologic research endeavor. Cancer Res. 2011 Jun 1;71(11):3889-95. doi: 10.1158/0008-5472.CAN-10-3932. Epub 2011 May 24.
Results Reference
background
PubMed Identifier
25876555
Citation
Phillips SM, Stampfer MJ, Chan JM, Giovannucci EL, Kenfield SA. Physical activity, sedentary behavior, and health-related quality of life in prostate cancer survivors in the health professionals follow-up study. J Cancer Surviv. 2015 Sep;9(3):500-11. doi: 10.1007/s11764-015-0426-2. Epub 2015 Apr 16.
Results Reference
background
PubMed Identifier
31720802
Citation
Steindorf K, Depenbusch J, Haussmann A, Tsiouris A, Schmidt L, Hermann S, Sieverding M, Wiskemann J, Ungar N. Change patterns and determinants of physical activity differ between breast, prostate, and colorectal cancer patients. Support Care Cancer. 2020 Jul;28(7):3207-3218. doi: 10.1007/s00520-019-05097-1. Epub 2019 Nov 13.
Results Reference
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PubMed Identifier
23296635
Citation
Blaney JM, Lowe-Strong A, Rankin-Watt J, Campbell A, Gracey JH. Cancer survivors' exercise barriers, facilitators and preferences in the context of fatigue, quality of life and physical activity participation: a questionnaire-survey. Psychooncology. 2013 Jan;22(1):186-94. doi: 10.1002/pon.2072. Epub 2011 Oct 6.
Results Reference
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PubMed Identifier
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Citation
Livingston PM, Craike MJ, Salmon J, Courneya KS, Gaskin CJ, Fraser SF, Mohebbi M, Broadbent S, Botti M, Kent B; ENGAGE Uro-Oncology Clinicians' Group. Effects of a clinician referral and exercise program for men who have completed active treatment for prostate cancer: A multicenter cluster randomized controlled trial (ENGAGE). Cancer. 2015 Aug 1;121(15):2646-54. doi: 10.1002/cncr.29385. Epub 2015 Apr 15.
Results Reference
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PubMed Identifier
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Citation
Tudor-Locke C, Lauzon N, Myers AM, Bell RC, Chan CB, McCargar L, Speechley M, Rodger NW. Effectiveness of the First step Program delivered by professionals versus peers. J Phys Act Health. 2009 Jul;6(4):456-62. doi: 10.1123/jpah.6.4.456.
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Impact of a Physical Activity Intervention With Motivational Support From Peers for Prostate Cancer Patients

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