Cancer Clinical Trial
— APA2Official title:
Adaptated Physical Activity During Chemotherapy: Evaluation of the Psychological, Physiological and Biological Impact
Although treatments significantly increase the life expectancy of cancer patients, their
quality of life is more or less reduced. The development of supportive care, such as
physical activity, is one of the tools that should be promoted to maintain quality of life
and reduce treatment side effects, including fatigue.
This study was developed to understand the different biopsychosocial effects of a physical
activity program carried out with patients suffering from various types of cancers, and to
facilitate and improve the implementation of this type of activity in health care
facilities.
Study randomized, controlled, cross-over intervention evaluating a 12-week supervised and
adapted physical activity program.
Participants were assigned to one of two groups: Group A which first follows a 12-week
physical activity program, then undergoes usual care for 12 additional weeks, or Group B,
which continues usual care for 12 weeks (control group) and then starts the physical
activity program for 12 additional weeks. Quality of life (with questionnaires for 2 groups)
, well-being, fatigue, physical capacity, leptin concentration, goal setting and level of
physical activity are evaluated during this protocol.
By understanding the multidimensional effects of a physical activity program for various
cancer types, depending on the time of proposing the program, by evaluating the correlations
among all these variables, and by evaluating long-term effects, the IPCAPA study contributes
to identifying the physical activity program which will be effective, viable and feasible
for all patients undergoing chemotherapy, whatever the type of cancer.
Status | Terminated |
Enrollment | 5 |
Est. completion date | August 2015 |
Est. primary completion date | August 2015 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patient aged 18 years or more, - Performance status (WHO) = 2 - Ability to participate in the IPCAPA program and medical certification of no contraindications to exercise - Availability and willingness to participate in the IPCAPA study for the duration of the protocol - Affiliated to a social security system - Signed informed consent. Exclusion Criteria: - Pregnant or breastfeeding woman. - Woman with childbirth ability without effective contraception. - Patient in emergency situations, adult subject to a measure of legal protection (major trusteeship, guardianship or ward of court), or unable to consent. - Inability to undergo medical monitoring of the trial for geographical, social or psychological reasons. - Inability to practice physical activity. - Planned surgery within 24 weeks of inclusion. |
Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Institut Paoli-Calmettes |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Impact of physical activity on fatigue during chemotherapy | Questionnaire MFI 20 (Multidimensional Fatigue Inventory) | From the inclusion in the protocol until week 24 | No |
Secondary | Physiological evaluation | 6-minute walk test | From the inclusion in the protocol until week 24 | No |
Secondary | Biological evaluation | Leptin level with a blood test | Leptin concentration realized from inclusion (week 1) then week 12 and week 24 | No |
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