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Multiple Interactive With Nutrition and Exercise Strategies in Frailty Cancer Patients

T

Tzu Chi University

Status

Unknown

Conditions

Cancer

Treatments

Behavioral: Nutrition and Exercise Strategies

Study type

Interventional

Funder types

Other

Identifiers

NCT04654637
TCU-CHHuang

Details and patient eligibility

About

Due to the changes in lifestyle caused by the COVID-19, it is a priority to provide multi-interactive digital platforms and social media for nutrition and exercise programs for cancer patients. A two-year serial program uses mixed study methods of longitudinal combined experimental study. We will investigate cancer frailty's current situation and track the frailty trends after cancer patients received different treatments. We will also invite experts to develop multi-interactive digital platforms of nutrition and performance-based tailored circuit training programs according to the cancer frailty survey. We will recruit 20-85 years of newly diagnosed or first-time recurrence cancer patients and stratified randomization assigned to evaluate nutrition and physical exercise intervention effectiveness. The measure indicators were treatment-related adverse events, nutritional status, frailty status, survival rate, and life quality.

Enrollment

128 estimated patients

Sex

All

Ages

20 to 85 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Aged from 20-85 years with histological confirmation malignancy.
  • Requiring treatment by surgery, chemotherapy, hormonotherapy, radiotherapy, or targeted therapy with a curative intention as estimated by oncologists.
  • First diagnosed or recurrence of head and neck cancer, esophageal cancer, colon/rectum cancer, lung cancer, AML, ALL, lymphoma, multiple myeloma.

Exclusion criteria

  • Non-head and neck cancer, esophageal cancer, colon/rectum cancer, lung cancer, AML, ALL, lymphoma, multiple myeloma with first diagnosis or recurrence patients.
  • Eastern Cooperative Oncology Group test score>2.
  • Serious psychiatric or cognitive problems, and functional disability leading to a total inability to walk.

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Single Blind

128 participants in 4 patient groups

Arm A
Experimental group
Description:
fix model of cycle exercise(online supervise) and routine nutrition consult
Treatment:
Behavioral: Nutrition and Exercise Strategies
Arm B
Experimental group
Description:
fix model of cycle exercise(online supervise) and online nutrition consult
Treatment:
Behavioral: Nutrition and Exercise Strategies
Arm C
Experimental group
Description:
individualize cycle exercise(online supervise) and routine nutrition consult
Treatment:
Behavioral: Nutrition and Exercise Strategies
Arm D
Experimental group
Description:
individualize cycle exercise(online supervise) and online nutrition consult
Treatment:
Behavioral: Nutrition and Exercise Strategies

Trial contacts and locations

1

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Central trial contact

Chu Hou Huang, PhD

Data sourced from clinicaltrials.gov

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