1. Electroacupuncture for the management of symptom clusters in cancer patients and survivors (EAST)
- Author
-
Xie, Lifang, Ng, Ding Quan, Heshmatipour, Matthew, Acharya, Munjal, Coluzzi, Paul, Guerrero, Nerida, Lee, Sanghoon, Malik, Shaista, Parajuli, Ritesh, Stark, Craig, Tain, Rongwen, Zabokrtsky, Keri, Torno, Lilibeth, and Chan, Alexandre
- Subjects
Health Services and Systems ,Nursing ,Health Sciences ,Traditional ,Complementary and Integrative Medicine ,Clinical Trials and Supportive Activities ,Complementary and Integrative Health ,Brain Disorders ,Neurosciences ,Mental Health ,Mind and Body ,Clinical Research ,Cancer ,Management of diseases and conditions ,7.1 Individual care needs ,Good Health and Well Being ,Child ,Humans ,Electroacupuncture ,Syndrome ,Treatment Outcome ,Neoplasms ,Survivors ,Symptom cluster ,Integrative oncology ,Randomized controlled trial ,Complementary and Alternative Medicine ,Complementary & Alternative Medicine ,Traditional ,complementary and integrative medicine - Abstract
BackgroundNeuropsychiatric symptoms, comprising cognitive impairment, fatigue, insomnia, depression, and anxiety, are prevalent and may co-occur during and after chemotherapy treatment for cancer. Electroacupuncture (EA), which involves mild electrical stimulation with acupuncture, holds great potential in addressing the management of individual symptoms. However, there is a lack of studies evaluating if EA can manage concurrent neuropsychiatric symptoms in cancer (i.e., symptom cluster). Hence, we designed a trial to evaluate the efficacy, safety, and feasibility of administering EA as an intervention to mitigate neuropsychiatric symptom clusters amongst cancer patients and survivors.MethodsThe EAST study is a randomized, sham-controlled, patient- and assessor-blinded clinical trial. Sixty-four cancer patients and survivors with complaints of one or more neuropsychiatric symptom(s) in the seven days prior to enrollment are recruited from the University of California Irvine (UCI) and Children's Hospital of Orange County (CHOC). Individuals with needle phobia, metastases, bleeding disorders, electronic implants, epilepsy, exposure to acupuncture in the three months prior to enrollment, and who are breastfeeding, pregnant, or planning to get pregnant during the duration of the study will be excluded. Screening for metal fragments and claustrophobia are performed prior to the optional neuroimaging procedures. Recruited patients will be randomized (1:1) in random blocks of four or six to receive either ten weekly verum EA (treatment arm, vEA) or weekly sham EA (control arm, sEA) treatment visits with a follow-up appointment four to twelve weeks after their last treatment visit. The treatment arm will receive EA at 13 acupuncture points (acupoints) chosen for their therapeutic effects, while the control arm receives minimal EA at 7 non-disease-related acupoints. Questionnaires and cognitive assessments are administered, and blood drawn to assess changes in symptom clusters and biomarkers, respectively.ConclusionThe EAST study can provide insight into the efficacy of EA, an integrative medicine modality, in the management of cancer symptom clusters in routine clinical practice.Trial registrationThis trial is registered with clinicaltrials.gov NCT05283577.
- Published
- 2023