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Trial Title: Using Combine Walking and Elastic Band to Decrease Fatigue

NCT ID: NCT05696275

Condition: Cancer Related Fatigue

Conditions: Official terms:
Fatigue

Study type: Interventional

Study phase: N/A

Overall status: Not yet recruiting

Study design:

Allocation: Randomized

Intervention model: Parallel Assignment

Primary purpose: Supportive Care

Masking: Single (Outcomes Assessor)

Intervention:

Intervention type: Behavioral
Intervention name: exercise
Description: 20-30 minutes of walking and elastic band exercise per day
Arm group label: exercise

Summary: This study is expected to propose an industry-university cooperation research case for the next two years. When cancer patients use ePRO to record subjective fatigue, and smart watches with 4G communication record objective fatigue, they will be given according to the patient's current degree of mild, moderate and severe fatigue. Suffer from 'exercise or activity' advice and lead the implementation of appropriate exercise advice. This study is expected to design aerobic + anaerobic exercise suitable for mild or moderate patients, and use the sensor of the smart watch to monitor the effect of exercise and fatigue. To sum up, the first-year plan is expected to use the established ePRO electronic records, combined with the LINE communication system, to integrate into a "cancer-related fatigue electronic registration and care system"; the second-year plan will integrate objective fatigue classifiers, Establish the exercise care option in the fatigue care system, and use the smart watch to establish a technology record function of the exercise process to help track the fatigue level of cancer patients.

Criteria for eligibility:
Criteria:
Inclusion Criteria: 1. age 20 years old; 2. diagnosis of cancer; 3. can continuous wearing bracelet for 14 days or more Exclusion Criteria: 1. Unclear and unable to answer the questionnaire; 2. Not able to walk; 3. platelet <50,000/mm3; 4. ANC 500/cumm

Gender: All

Minimum age: 20 Years

Maximum age: N/A

Healthy volunteers: No

Start date: January 16, 2023

Completion date: December 31, 2024

Lead sponsor:
Agency: Taipei Medical University
Agency class: Other

Source: Taipei Medical University

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT05696275

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