About this trial
The academic community generally believes that cancer symptom clusters (CSCs) are not independent diseases, but a group of symptoms that accompany cancer patients. Based on etiology, they can be classified into CSCs related to tumor progression, CSCs related to cancer treatment, or a combination of both. According to symptom manifestations, they can be divided into psychological symptom CSCs, somatic symptom CSCs, and CSCs with coexisting psychological and somatic symptoms. CSCs are universally present during the progression or treatment of cancer. Traditional Chinese medicine (TCM) can leverage its unique characteristics in the intervention of symptom clusters and symptom management. This study is planned to conduct a high-level, prospective, multicenter, randomized, double-blind, placebo-controlled trial to evaluate the efficacy and safety of a TCM regimen for cancer symptom clusters (CSCs), and to simultaneously analyze the characteristics of the population that may benefit most from TCM treatment for CSCs.
Eligibility criteria
Qualifiers
Histologically or cytologically confirmed primary epithelial ovarian cancer
Meet diagnostic criteria for chronic insomnia defined by the Sleep Disorders Group of the Neurology Branch of the Chinese Medical Association: Pittsburgh Sleep Quality Index (PSQI) total score >8 Piper Fatigue Scale total score >4 and Patient Health Questionnaire-9 (PHQ-9) total score >5
Moderate-to-severe symptom severity (average score ≥4 on the MD Anderson Symptom Inventory for Ovarian Cancer [MDASI-OC] subscale assessing sleep disturbance-fatigue-distress-sadness)
Eastern Cooperative Oncology Group Performance Status (ECOG-PS) score 0-2;
Disqualifiers
Patients scheduled to undergo radiotherapy within the next 4 treatment cycles
Comorbid severe primary diseases of the heart, brain, liver, kidney, or hematopoietic system, including hepatic dysfunction (AST/ALT >1.5 times the upper limit of normal [ULN]) or renal impairment (serum creatinine [Cr] >1.2 times ULN)
Pregnant or lactating women, individuals with psychiatric disorders (e.g., schizophrenia, bipolar disorder, mania, depression, anxiety disorders, phobias), intellectual/language impairments, or other mental health conditions;
Scores ≥15 on the Patient Health Questionnaire (PHQ-9) for depression or ≥15 on the Generalized Anxiety Disorder-7 (GAD-7) at screening
Trial design
Treatments tested in this trial
- Compound Ciwujia Granules
- Placebo granules
- Standard treatment protocol for ovarian cancer combined with psychological intervention.
Treatment groups
Locations
Sponsors and collaborators
Shanghai Municipal Hospital of Traditional Chinese Medicine
Lead sponsor
Guangdong Provincial Hospital of Traditional Chinese Medicine
Collaborator
Affiliated Hospital of Qinghai University
Collaborator
Obstetrics & Gynecology Hospital of Fudan University
Collaborator
Fudan University
Collaborator
Beijing Hospital of Traditional Chinese Medicine
Collaborator