Clinical trial · Interventional
Real-time Interactive Digital Healthcare System in Post Operation Patients With Breast Cancer; Pilot Study
Hospital-home Linkage Short-term Rehabilitation Therapy Using Real-time Interactive Digital Healthcare System in Post Operation Patients With Breast Cancer; Pilot Study
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This study aims to examine the effect of hospital-home linkage short-term rehabilitation therapy using real-time interactive digital healthcare system (Uincare Homeplus) in post-operative patients with breast cancer. This is prospective pilot study. 20 breast cancer patients who underwent wide local excision-axillary lymph node diessection or modified radical mastectomy will be examined, and those with limited range of motion (ROM) of affected shoulder will be enrolled in the study. Shoulder ROM, Quick-DASH, pain evaluation with NRS, quality of life evaluation with FACT-B and EQ-5D will be evaluated on enrollment, 4-week, 8-week, and 12-weeks after enrollment.
Conditions
Conditions (2)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Rehabilitation | — | UNRESOLVED | — |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Uincare | Device | — | UNRESOLVED |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Uincare
- description
- Exercise using Uincare
- interventionNames
- Device: Uincare
Primary outcomes (1)
- measure
- Range of motion of affected shoulder
- timeFrame
- Enrollment, 4 week, 8 week, 12 week
- description
- Evaluation of change of range of motion of the affected shoulder from baseline to 12 weeks
Secondary outcomes (4)
- measure
- Numerical rating scale of affected shoulder
- timeFrame
- Enrollment, 4 week, 8 week, 12 week
- description
Eligibility
Eligibility (as posted)
- Sex
- Female
- Minimum age
- 30 Years
- Maximum age
- 70 Years
Show eligibility criteria text
Inclusion Criteria: * Patients who underwent breast cancer surgery (wide local excision-axillary lymph node dissection or modified radical mastectomy) * Limited active/passive range of motion of the affected shoulder (Flexion \<160' or Abduction \<160') * post-operative day not exceeding 8 week * Patients who agreed informed consent Exclusion Criteria: * Bilateral breast cancer surgery * Patients with shoulder pain of limited ROM before breast cancer surgery * Those unable to perform exercise due to general deconditioning * Those with communication difficulty
References
Publications (0)
Data not yet available