Breast Cancer Clinical Trial
Official title:
An Assessor-Blinded, Randomised Controlled Trial of Acupuncture to Prevent Chemobrain in Breast Cancer Patients
NCT number | NCT02457039 |
Other study ID # | UW 14-206 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | October 2015 |
Est. completion date | March 2019 |
Verified date | May 2019 |
Source | The University of Hong Kong |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Chemobrain is an expression used to describe a cluster of chemotherapy-induced cognitive
impairment symptoms, including problems with visual and verbal memory, forgetfulness,
difficulty in learning, attention, concentration and coordination of multitasking and
organization. Over 75% cancer patients experienced acute cognitive symptoms during
chemotherapy and 17%-34% of them have long-term post-treatment cognitive deficits which can
persist up to 10 years. Breast cancer survivors even display as high as 50%-75% prevalence of
post-treatment cognitive impairment. Chemobrain has become an apparent quality-of-life issue
for cancer survivors and will be encountered more frequently with the rise of the number of
cancer survivors. There are no effective interventions available for preventing and treating
chemobrain.
Acupuncture is beneficial in reducing various side effects of anti-cancer treatment. It also
shows the efficacy in improving mild cognitive impairment and other dementia disorders;
facilitates the recovery of pathological microstructural changes of the brain. These results
have led to the hypothesis that acupuncture is effective in preventing chemobrain and this
preventive effect may be associated with the protection against cytokine production,
epigenetic modification and microstructural changes of the brain.
To test this hypothesis, an assessor-blinded, randomised controlled trial will be conducted
to determine if a combination of DCEAS and body acupuncture could reduce the incidence and
symptoms of chemobrain in breast cancer patients under chemotherapy compared to least
acupuncture stimulation (LAS) as controls.
A total of 168 breast cancer patients who are ready for chemotherapy will be randomly
assigned to comprehensive acupuncture intervention (combined DCEAS and body acupuncture
regimen + chemotherapy) (CAI) (n = 84) for 2 sessions per week for 8 weeks or least
acupuncture stimulation (LAS) (minimal acupuncture + chemotherapy) (n = 84). All patients
receive the standard chemotherapy of breast cancer. Treatment outcomes on cognitive
performance, fatigue and the depression will be assessed.
Status | Completed |
Enrollment | 93 |
Est. completion date | March 2019 |
Est. primary completion date | December 2018 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: 1. Chinese females aged 18 to 65 years; 2. have a diagnosis of stage I-IIIa breast cancer; and 3. are ready for orally administered or vein injection or both with Cytoxan-containing regimens as adjuvant chemotherapy before or after surgical treatment or in combination with other pharmacotherapy. Exclusion Criteria: 1. had chemotherapy in the last 2 years; 2. have cardiac pacemakers, epilepsy or other unstable medical conditions; 3. had investigational drug treatment within the past 6 months; 4. alcoholism or drug abuse within the past 1 year; or 5. have severe needle phobia. |
Country | Name | City | State |
---|---|---|---|
China | Department of Chinese Medicine, The University of Hong Kong - Shenzhen Hospital | Shenzhen | Guangdong |
China | Department of Clinical Oncology, The University of Hong Kong - Shenzhen Hospital | Shenzhen | Guangdong |
Hong Kong | Department of Clinical Oncology, Queen Mary Hospital | Hong Kong | |
Hong Kong | Department of Surgery, Queen Mary Hospital | Hong kong | |
Hong Kong | Department of Surgery, Tung Wah Hospital | Sai Ying Pun | |
Hong Kong | The Nethersole School of Nursing, The Chinese University of Hong Kong | Sha Tin | N.t. |
Lead Sponsor | Collaborator |
---|---|
The University of Hong Kong | Chinese University of Hong Kong |
China, Hong Kong,
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* Note: There are 39 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in cognitive function (objective measurement) | The Montreal Cognitive Assessment (MoCA) of corresponding dialects will be used as an objective measurement for subjects' cognitive function. Assessments will be conducted at baseline and every 2 weeks thereafter. | Baseline, 2 week, 4 week, 6 week, 8 week | |
Primary | Changes in cognitive function (subjective measurement) | The Functional Assessment of Cancer Therapy-Cognitive Function (FACT-Cog) of corresponding dialects will be used as a subjective measurement for subjects' cognitive function. Assessments will be conducted at baseline and every 2 weeks thereafter. | Baseline, 2 week, 4 week, 6 week, 8 week | |
Secondary | Changes in quality of Life - composite measure | The European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (QLQ-C30+BR23) and Functional Assessment of Cancer Therapy-Breast (FACT-B) of corresponding dialects will be used for assessment on quality of life. Both of them will be used as the former focuses on physical function, while the latter emphasizes on emotional well-being. Assessments will be conducted at baseline and every 4 weeks thereafter. | Baseline, 4 week, 8 week | |
Secondary | Changes in illness related fatigue measured by FACIT-Fatigue | As fatigue is a common co-morbidity observed in patients receiving chemotherapy, it will be measured using the Functional Assessment of Chronic Illness Therapy-Fatigue (FACIT-Fatigue) of corresponding dialects. Assessments will be conducted at baseline and every 4 weeks thereafter. | Baseline, 4 week, 8 week | |
Secondary | Changes in chemo adverse effects - composite measure | Adverse side effects will be assessed using Functional Assessment of Cancer Therapy questionnaires (FACT-Taxane, FACT-BRM) of corresponding dialects. Assessments will be conducted at baseline and every 4 weeks thereafter. | Baseline, 4 week, 8 week | |
Secondary | Changes in subject perception of chemotherapy treatment measured by FACIT-TS-G | To determine whether acupuncture can reduce the adverse effects of chemo-therapy treatment and therefore increase subject acceptance, subject treatment satisfaction will be assessed using Functional Assessment of Chronic Illness Therapy questionnaire (FACIT-TS-G). Assessments will be conducted at baseline and every 4 weeks thereafter. | Baseline, 4 week, 8 week |
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