Feasibility of a Modular mHealth for Tailored Rehabilitation of Breast Cancer (MMHTR)
Status
Conditions
Treatments
Details and patient eligibility
About
This study investigated the feasibility of the novel modular mobile health (mHealth) for personalized rehabilitation and explored the participants' satisfaction and app data during treatment of breast cancer.
Full description
This is prospective, feasible, parallel study in post-operative patients with breast cancer and during treatment. Disability of Arm, Shoulder, Hands (DASH), Physical activity data (IPAQ-SF), Physical measurement such as hand grip strength, body mass index (BMI), muscle mass, and differences in arm circumference, PRO-CTCAE, Distress Thermometer, needs and satisfaction in app, personal health record of app (exercise, daily step count, etc.) Measure will be evaluated on 1-month, 2-month, 4-month, 6-month, 9-month, and 12-month after POD.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Unilateral breast cancer at TNM stage 0 ~ III
- Patients who will undergo the treatment (chemotherapy, radiation therapy, and hormone therapy) after surgery
- Patients who had a mobile phone (Android or iOS)
Exclusion criteria
- Patients who have metastases or recurrence to other organs were excluded
Trial design
Primary purpose
Allocation
Interventional model
Masking
44 participants in 2 patient groups
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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