search
Back to results

Clinical Trial: Effectiveness and Efficiency of Physical Exercise in Cancer Patients (EFICANCER)

Primary Purpose

Non-Small-Cell Lung Carcinoma, Digestive System Neoplasms, Breast Neoplasms

Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Supervised Physical activity
education program on healthy habits
Sponsored by
Basque Health Service
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Non-Small-Cell Lung Carcinoma focused on measuring physical exercise, Health Related Quality of Life, Non-Small-Cell Lung Carcinoma, digestive system neoplasms, breast neoplasms

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age between 18-70 years
  • Diagnosis of digestive system cancer , breast cancer or histologically confirmed NSCLC stage IV Physical Status (PS) 0 or 1.
  • First-line chemotherapy treatment for each type of standard tumor
  • Adequate renal, liver and blood function.

Exclusion Criteria:

  • Brain metastases
  • Risk of fracture (bone metastases)
  • Unstable heart disease, uncontrolled BP Systolic Blood Pressure((SBP)> 200 or Diastolic Blood Pressure (DBP)> 110), heart failure (NYHA II or greater), constrictive pericarditis
  • Other diseases at the discretion of the investigator to be a contraindication for physical exercise.
  • Perform regular physical activity (150 minutes / week of moderate or vigorous 75)

Sites / Locations

  • Primary Care Research Unit of BizkaiaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Exercise group

control group

Arm Description

supervised exercise program education program on healthy habits Pharmacological treatment and selfcare encouragement

Pharmacological treatment and selfcare encouragement.

Outcomes

Primary Outcome Measures

Changes in Health Related Quality of Life (EORTC QLQ-C30)

Secondary Outcome Measures

asthenia measurement with FACIT-F (Functional Assessment of Chronic Illness Therapy-Fatigue) questionaire
Functional Capacity-6 minute Walking test
cardiorespiratory test
Changes in Muscular Strenght-Dynamometer
progression-free survival

Full Information

First Posted
February 5, 2013
Last Updated
July 22, 2014
Sponsor
Basque Health Service
search

1. Study Identification

Unique Protocol Identification Number
NCT01786122
Brief Title
Clinical Trial: Effectiveness and Efficiency of Physical Exercise in Cancer Patients
Acronym
EFICANCER
Official Title
PHYSICAL EXERCISE TO IMPROVE THE QUALITY OF LIFE OF CANCER PATIENTS DURING TREATMENT PROCESS: EFICANCER STUDY
Study Type
Interventional

2. Study Status

Record Verification Date
July 2014
Overall Recruitment Status
Unknown status
Study Start Date
April 2013 (undefined)
Primary Completion Date
January 2015 (Anticipated)
Study Completion Date
December 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Basque Health Service

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
AIM: To evaluate the effectiveness and efficiency of an innovative exercise program (EP) for patients during treatment for gastrointestinal tumors, breast and non small cells lung cancer, in terms of improved quality of life (QOL), fatigue and functional capacity respect the usual standard treatment (ST). DESIGN: Pragmatic randomized clinical trial in two parallel groups: EP and ST. SETTING: 7 Primary Health Centers (PHC) of the redIAPPISCIII, in coordination with oncology services. PARTICIPANTS: 250 patients with the above tumors, locally advanced or with metastatic disease, in adjuvant treatment, with Performance Status(PS) PS1-PS0. INTERVENTION: Both groups received standardized usual care. The EP group will receive, in addition, a nurse supervised exercise program for 2 months in the PHC and a second phase in community facilities during the remaining 10 months. MEASUREMENTS: The primary outcome measure is the change from baseline in the QOL+66 treatment, as measured by the specific questionnaire for patients with cancer EORTC QLQ-C-30 and Short Form(SF-36) overall. Secondary: fatigue (FACIT-F), radiological response, functional capacity (6 minutes walking and cardiopulmonary test), muscle strength and progression-free survival and overall. Predictors and confounders: age, sex, stage and tumor type, histology, treatment. ANALYSIS: We will compare between groups mean changes from baseline measurement of quality of life questionnaire (QOL) and other variables, on an intention to treat basis, using longitudinal mixed-effects models for repeated measures at 2, 6 and 12 months follow-up. Cost / effectiveness and cost / incremental utility associated to the program wil be estimated.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Non-Small-Cell Lung Carcinoma, Digestive System Neoplasms, Breast Neoplasms
Keywords
physical exercise, Health Related Quality of Life, Non-Small-Cell Lung Carcinoma, digestive system neoplasms, breast neoplasms

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Exercise group
Arm Type
Experimental
Arm Description
supervised exercise program education program on healthy habits Pharmacological treatment and selfcare encouragement
Arm Title
control group
Arm Type
No Intervention
Arm Description
Pharmacological treatment and selfcare encouragement.
Intervention Type
Other
Intervention Name(s)
Supervised Physical activity
Intervention Description
Both groups received standardized usual care. The EP group will receive, in addition, a nurse supervised exercise program for 2 months in the PHC and a second phase in community facilities during the remaining 10 month
Intervention Type
Behavioral
Intervention Name(s)
education program on healthy habits
Intervention Description
education program on healthy habits for 2 months in the PHC and a second phase in community facilities during the remaining 10 months
Primary Outcome Measure Information:
Title
Changes in Health Related Quality of Life (EORTC QLQ-C30)
Time Frame
basal,2,6,12 months fllow up
Secondary Outcome Measure Information:
Title
asthenia measurement with FACIT-F (Functional Assessment of Chronic Illness Therapy-Fatigue) questionaire
Time Frame
Basal, 2,6 and12 months
Title
Functional Capacity-6 minute Walking test
Time Frame
basal, 2,6 and 12 months
Title
cardiorespiratory test
Time Frame
basal, 2, 6 and12 months
Title
Changes in Muscular Strenght-Dynamometer
Time Frame
basal, 2,6 nad 12 months
Title
progression-free survival
Time Frame
basal, 2, 6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age between 18-70 years Diagnosis of digestive system cancer , breast cancer or histologically confirmed NSCLC stage IV Physical Status (PS) 0 or 1. First-line chemotherapy treatment for each type of standard tumor Adequate renal, liver and blood function. Exclusion Criteria: Brain metastases Risk of fracture (bone metastases) Unstable heart disease, uncontrolled BP Systolic Blood Pressure((SBP)> 200 or Diastolic Blood Pressure (DBP)> 110), heart failure (NYHA II or greater), constrictive pericarditis Other diseases at the discretion of the investigator to be a contraindication for physical exercise. Perform regular physical activity (150 minutes / week of moderate or vigorous 75)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Gonzalo Grandes, Medicine
Phone
0034946006637
Email
GONZALO.GRANDESODRIOZOLA@osakidetza.net
First Name & Middle Initial & Last Name or Official Title & Degree
Maria Soledad Arietaleanisbeaskoa, Nurse
Phone
0034946006637
Email
MARIASOLEDAD.ARIETALEANIZBEASCOASARABIA@osakidetza.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
GRANDES GONZALO, Medicine
Organizational Affiliation
Primary Care Research Unit of Bizkaia (Basque Health Service)
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
ARIETALEANIZBEASCOA MARIA SOLEDAD, NURSE
Organizational Affiliation
Primary Care Research Unit of Bizkaia (Basque Health Service)
Official's Role
Study Director
Facility Information:
Facility Name
Primary Care Research Unit of Bizkaia
City
Bilbao
State/Province
Bizkaia
ZIP/Postal Code
48014
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
ARIETALEANIZBEASCOA MARISOL, NURSE
Phone
946006637
Email
MARIASOLEDAD.ARIETALEANIZBEASCOASARABIA@osakidetza.net
First Name & Middle Initial & Last Name & Degree
ARCE ARANA, NURSE
Phone
946006637
Email
VERONICA.ARCEARANA@osakidetza.net

12. IPD Sharing Statement

Citations:
PubMed Identifier
25655792
Citation
Sancho A, Carrera S, Arietaleanizbeascoa M, Arce V, Gallastegui NM, Gine March A, Sanz-Guinea A, Eskisabel A, Rodriguez AL, Martin RA, Lopez-Vivanco G, Grandes G. Supervised physical exercise to improve the quality of life of cancer patients: the EFICANCER randomised controlled trial. BMC Cancer. 2015 Feb 6;15:40. doi: 10.1186/s12885-015-1055-x.
Results Reference
derived

Learn more about this trial

Clinical Trial: Effectiveness and Efficiency of Physical Exercise in Cancer Patients

We'll reach out to this number within 24 hrs