ClinicalTrials.gg
CompletedNCT07445243Updated Mar 3, 2026

Integrated Chinese and Western Therapy for Cancer-Related Fatigue

An interventional study of Integrated Chinese and Western Holistic Care Program in Cancer-related Fatigue and Neoplasms (Cancer / Tumors), sponsored by Taichung Tzu Chi Hospital. Completed at 1 site in Taiwan. Open to participants aged 20 Years to 95 Years. Per ClinicalTrials.gov, last updated 2026-03-03.

Sponsored by Taichung Tzu Chi Hospital · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 6 years 3 months after the study started (first participant enrolled Nov 2019, registered Feb 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
86
Allocation
Not applicable
Ages
20 Years to 95 Years
Sex
All
01

Study summary

Cancer-related fatigue (CRF) is a common and debilitating symptom in patients with cancer. Evidence-based non-pharmacological approaches include sleep hygiene, physical activity, nutritional management, and traditional Chinese medicine (TCM). This study evaluates the clinical effectiveness of an interdisciplinary holistic program integrating Chinese and Western therapies for CRF among hospitalized cancer patients receiving integrated care. Approximately 100 participants will be enrolled and followed for up to 3 months.

Read the detailed description

Eligible hospitalized cancer patients receiving integrated Chinese and Western care will be enrolled after providing informed consent. Participants will complete a CRF questionnaire and receive a non-invasive holistic integrative care program, including patient education, sleep hygiene, exercise guidance, nutritional assessment/intervention, and TCM-related care. The primary endpoint is change in CRF score. Secondary endpoints include TCM constitution assessment, vital signs, anthropometrics, complete blood count, and liver/renal function tests. Participants will be followed for 3 months from enrollment.

02

Conditions studied

  • Cancer-related Fatigue
  • Neoplasms (Cancer / Tumors)

Keywords

  • Holistic care
  • Integrative medicine
  • Integrated Chinese and Western medicine
  • Traditional Chinese Medicine
  • Chinese herbal medicine
  • Sleep hygiene
  • Aromatherapy
  • Nutrition counseling
  • Oncology nursing
  • Cancer-related fatigue
03

In context

Neoplasms

10,818 studies on the registry are indexed under Neoplasms; 2,324 are open to participants now.

This study's enrollment of 86 is above the median of 60 across 7,703 interventional studies indexed under Neoplasms.

Browse Neoplasms studies →

Lead sponsor

Taichung Tzu Chi Hospital is the lead sponsor of 17 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 95 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:

  • Inclusion Criteria:

Signed form.

Age 20 to 95 years.

Receiving integrated Chinese and Western holistic care.

Agree to provide data for this study.

Exclusion Criteria:

Refuse to continue participation during the study period, or the family requests discontinuation (withdrawal).

Psychiatric disorder that makes the participant unable to cooperate.

Exclusion Criteria:

-

Terms in these criteria, in plain language(2)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
86 participants (actual)

Study arms

  • Experimental
    Integrated Chinese and Western Holistic Care

    All participants receive an integrated Chinese and Western holistic care program during hospitalization for cancer-related fatigue management. The program includes routine fatigue assessment and individualized supportive care measures (education, sleep hygiene, exercise encouragement, aromatherapy and/or massage, nutrition consultation, and shared decision-making). Traditional Chinese Medicine consultation (e.g., acupuncture and/or Chinese herbal medicine) may be provided when clinically indicated.

    Other: Integrated Chinese and Western Holistic Care Program

Interventions

  • OtherIntegrated Chinese and Western Holistic Care Program

    An interdisciplinary integrative care program combining Western supportive care and Traditional Chinese Medicine to manage cancer-related fatigue in hospitalized oncology patients. Core components include fatigue assessment, patient education and symptom management guidance, sleep hygiene, exercise encouragement, aromatherapy and/or massage, nutrition assessment and counseling, and shared decision-making. Traditional Chinese Medicine consultation may provide acupuncture and/or Chinese herbal medicine according to patient needs and clinical judgment.

06

What researchers measure

Primary outcomes

  1. Change in Cancer-Related Fatigue (CRF) Score (0-10)

    CRF is assessed using the Taiwan Society of Cancer Palliative Medicine fatigue scale (0-10) during hospitalization. Peak CRF score is defined as the maximum recorded CRF score from admission to discharge. Discharge CRF score is defined as the last in-hospital CRF assessment prior to discharge. The primary outcome is the within-participant change in CRF score from peak to discharge.

    Time frame: From admission (baseline) through discharge (last in-hospital assessment; up to 30 days)

Secondary outcomes

  1. Proportion of Participants With Moderate-to-Profound CRF at Discharge (CRF Score ≥4)

    Percentage of participants whose discharge CRF score is ≥4 (moderate or above) on the Taiwan Society of Cancer Palliative Medicine fatigue scale (0-10).

    Time frame: At discharge (last in-hospital assessment; up to 30 days after admission)

  2. Distribution of CRF Severity Categories at Discharge (0, 1-3, 4-6, 7-8, 9-10)

    Distribution of discharge CRF scores categorized as 0, 1-3, 4-6, 7-8, and 9-10 on the Taiwan Society of Cancer Palliative Medicine fatigue scale.

    Time frame: At discharge (last in-hospital assessment; up to 30 days after admission)

07

Study locations

1 site
  • Taichung Tzu Chi Hospital
    Taichung, 42743, Taiwan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 3, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07445243
Lead sponsor
Taichung Tzu Chi Hospital
Responsible party
Chia-Ying Chuang (Attending Physician, Taichung Tzu Chi Hospital) — Principal investigator
First posted
Mar 3, 2026
Start date
Nov 8, 2019
Primary completion
Apr 22, 2020
Completion
Apr 22, 2020
Last update
Mar 3, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion