Title

Health-related Quality of Life-intervention in Survivors of Breast and Other Cancers Experiencing Cancer-related Fatigue Using Traditional Chinese Medicine: The HERBAL Trial
HEalth-Related Quality of Life-intervention in Survivors of Breast and Other Cancers Experiencing Cancer-related Fatigue Using TraditionAL Chinese Medicine: The HERBAL Trial
  • Phase

    Phase 2
  • Study Type

    Interventional
  • Status

    Unknown status
  • Study Participants

    80
This study is a phase 2, randomized, double-blinded, placebo-controlled trial to evaluate the efficacy and safety of a Traditional Chinese Medicine decoction, the modified Xiang Bei Yang Rong Tang, in alleviating cancer related fatigue in cancer survivors.
Cancer-related fatigue (CRF) is a distressing, persistent and subjective sense of physical, emotional, or cognitive tiredness related to cancer or its treatment. Currently there is a lack of effective conventional pharmacological intervention for treating this condition. Traditional Chinese Medicine (TCM) could be alternative therapy for managing CRF.

This study is a phase 2, randomized, double-blinded, placebo-controlled trial to examine the efficacy and safety of a TCM decoction, the modified Xiang Bei Yang Rong Tang (XBYRT) in alleviating CRF in cancer survivors. Study participants recruited from National Cancer Centre Singapore (NCCS) will be randomized to receive either the XBYRT or placebo decoction. Participants will take their assigned decoction daily for a duration of 8 weeks and will be assessed using patient reported outcome (PRO) questionnaires. PROs used are the European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC-QLQ 30) for QOL, the Multidimensional Fatigue Symptom Inventory Short Form (MFSI-SF) for fatigue and Functional Assessment of Cancer Therapy-Cognitive Function (FACT-Cog) Version 3 for cognitive abilities. The changes in scores measured by these assessment tools will be compared between the XBYRT intervention and placebo groups. Blood biomarkers such as inflammatory cytokines, mitochondrial DNA and oxidative stress markers will also be evaluated in the study participants. Additionally, adverse events or serious adverse events in participants will be monitored for safety.

Results from this study will provide a better understanding on the role of TCM in managing CRF.
Study Started
Oct 24
2019
Primary Completion
May 30
2021
Anticipated
Study Completion
Jun 09
2022
Anticipated
Last Update
Jun 16
2020

Other Modified Xiang Bei Yang Rong Tang

Modified Xiang Bei Yang Rong Tang is a combination of 15 herbal components and it is available in granules form to be dissolved in hot water for consumption

Other Placebo

Placebo granules contain 5% XBYRT, colourant, bitterant and 95% starch filler

XBYRT decoction Experimental

Participants assigned to receive the modifed Xiang Bei Yang Rong Tang granules

Placebo Placebo Comparator

Participants assigned to receive placebo (contains 5% of XBYRT) granules

Criteria

Inclusion Criteria:

Age ≥21 years
Clinically diagnosed cancer (Stages I-III)
Completed surgery/chemotherapy/radiotherapy for at least 1 month
At least one month after starting on aromatase inhibitors or ovarian suppression for breast cancer survivors
Not expected to receive surgery/chemotherapy/radiotherapy next 10 weeks
Fatigue screening score ≥4 for past 7 days
Life expectancy ≥3 months
Patients satisfy TCM syndrome differentiation as qi and blood deficiency Experience 2 major symptoms coupled with typical tongue and pulse conditions; 2 major symptoms and 1 possible symptom coupled with tongue and pulse conditions; 1 major symptom and at least 2 possible symptoms coupled with tongue and pulse conditions
Able to read and understand English or Mandarin

Exclusion Criteria:

Cancer recurrence and/or metastasis
Untreated co-morbidities causing fatigue (e.g. Severe anaemia, thyroid disorder)
On medications that cause fatigue (e.g. beta blockers)
Patients on warfarin
Cancer survivors receiving adjuvant therapy during the study period. Aromatase inhibitors and anti-HER2 monoclonal antibodies are acceptable.
Receiving or planning to receive treatment from other TCM practitioners during the study period
Breast feeding or intending to conceive/get pregnant during the study treatment period
Patients who present with yin deficiency and deficiency syndromes (e.g. phlegm-dampness, blood stasis, toxic-heat and qi stagnation)
No Results Posted