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Trial Title:
Effects of an Exercise Intervention on Taxane-induced Peripheral Neuropathy in Breast Cancer Survivors
NCT ID:
NCT05641571
Condition:
CIPN - Chemotherapy-Induced Peripheral Neuropathy
Conditions: Official terms:
Peripheral Nervous System Diseases
Conditions: Keywords:
Taxane-induced peripheral neuropathy, extremity exercise
Study type:
Interventional
Study phase:
N/A
Overall status:
Unknown status
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Intervention model description:
The 3~6 months home-based extremity exercise program will be intervened between newly
diagnosed with breast cancer to the completion of chemotherapy. Participants have to
perform a total of 50 minutes of exercise including the Ten Skilled Hand exercise fourth
a day, 5 minutes each time and Buerger Allen exercise twice a day, 15 minutes each time.
The observational group will need to record the extra exercise performed and the exercise
prescription will be distributed after the study.
Primary purpose:
Prevention
Masking:
None (Open Label)
Intervention:
Intervention type:
Behavioral
Intervention name:
The home-based extremity exercise program
Description:
Participants have to perform a total of 50 minutes of exercise including the Ten Skilled
Hand exercise fourth a day, 5 minutes each time and Buerger Allen exercise twice a day,
15 minutes each time before chemotherapy to the completion of chemotherapy.
Arm group label:
Exercise group
Summary:
The purpose of this study is to examine the effects of an exercise program on the
management of TIPN in breast cancer survivors. This experimental study utilizes purposive
sampling to recruit 88 adults, newly diagnosed with stage I~III breast cancer women, who
are expected to be treated with Taxane chemotherapy in a medical center located in
central Taiwan. Participants will be randomly allocated to the experimental or
observational group. The main outcomes are peripheral neuropathy and neuropathic pain.
The 3~6 months home-based extremity exercise program will be intervened between newly
diagnosed with breast cancer to the completion of chemotherapy. Participants have to
perform a total of 50 minutes of exercise including the Ten Skilled Hand exercise fourth
a day, 5 minutes each time and Buerger Allen exercise twice a day, 15 minutes each time.
This study expects that the extremity exercise program will be able to prevent and manage
peripheral neuropathy and neuropathic pain via increasing blood circulation. Moreover,
the exercise program may also improve functioning and QOL in breast cancer survivors
receiving Taxane chemotherapy.
Detailed description:
The incidence of breast cancer increases yearly. Taxane is one of the main chemotherapy
drugs for breast cancer treatment. Taxane-induced peripheral neuropathy (TIPN) impairs
breast cancer survivors' functioning, increases the risk of falls, and impacts quality of
life (QOL). As TIPN worsens, there is a need to decrease chemotherapy dosage or terminate
treatment. This may reduce the effect of chemotherapy, in addition, to increasing
survivor's mortality. Up to date, no evidence-based, effective nonpharmacologic
intervention to prevent or manage TIPN. Furthermore, no interventions were recommended by
the U.S. Food and Drug Administration or TIPN expert organizations to prevent or treat
TIPN. Therefore, the purpose of this study is to examine the effects of an exercise
program on the management of TIPN in breast cancer survivors.
This experimental study utilizes purposive sampling to recruit 88 adults, newly diagnosed
with stage I~III breast cancer women, who are expected to be treated with Taxane
chemotherapy in a medical center located in central Taiwan. Participants will be randomly
allocated to the experimental or observational group using the two strata: (1) adjuvant
or neoadjuvant and (2) paclitaxel, docetaxel, or Taxane plus Platinum. Participants who
have peripheral neuropathy before chemotherapy or regular exercise are excluded. The
four-measure points are as the followings: (T1) before chemotherapy, (T2) after the
completion of the first Taxane, (T3) the completion of half chemotherapy regimen, and
(T4) the completion of chemotherapy. The main outcomes are peripheral neuropathy and
neuropathic pain. The blood circulation of extremities, functional status, falls and QOL
are also measured. SPSS 22 is used to enter and analyze data. Mean, standard deviation,
frequency, and percentage are utilized to describe the distribution of the sample and
research variables. Chi-squared and generalized estimating equation is used to detect the
difference and change over time between the two groups.
The 3~6 months home-based extremity exercise program will be intervened between newly
diagnosed with breast cancer to the completion of chemotherapy. Participants have to
perform a total of 50 minutes of exercise including the Ten Skilled Hand exercise fourth
a day, 5 minutes each time and Buerger Allen exercise twice a day, 15 minutes each time.
The observational group will need to record the extra exercise performed and the exercise
prescription will be distributed after the study. This study expects that the extremity
exercise program will be able to prevent and manage peripheral neuropathy and neuropathic
pain via increasing blood circulation. Moreover, the exercise program may also improve
functioning and QOL in breast cancer survivors receiving Taxane chemotherapy.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- Participants will be randomly allocated to the experimental or observational group
using the two strata: (1) adjuvant or neoadjuvant and (2) paclitaxel, docetaxel, or
Taxane plus Platinum.
Exclusion Criteria:
- Participants who have peripheral neuropathy before chemotherapy or regular exercise
are excluded.
Gender:
Female
Minimum age:
20 Years
Maximum age:
99 Years
Healthy volunteers:
No
Start date:
December 1, 2022
Completion date:
December 31, 2023
Lead sponsor:
Agency:
Taichung Veterans General Hospital
Agency class:
Other
Source:
Taichung Veterans General Hospital
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05641571