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Real-time Interactive Digital Healthcare System in Patients With Breast Cancer; Randomized Controlled Trial

Primary Purpose

Breast Cancer

Status
Completed
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Uincare Homeplus
Brochure
Sponsored by
Samsung Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Breast Cancer

Eligibility Criteria

20 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients who underwent breast cancer surgery (axillary lymph node dissection or breast reconstruction following 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 and limited ROM before breast cancer surgery
  • Those unable to perform exercise due to general deconditioning
  • Those with communication difficulty

Sites / Locations

  • Samsung Medical Center
  • Department of rehabilitation, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Exercise using Uincare Homeplus

Exercise using brochure

Arm Description

Uincare Homeplus

brochure

Outcomes

Primary Outcome Measures

Range of motion in affected shoulder
Evaluation of change in range of motion of the affected shoulder from baseline to 12 weeks

Secondary Outcome Measures

Numerical rating scale of affected shoulder
Evaluation of pain in the affected shoulder using numerical rating scale minimum ~ maximum value: 0 ~ 10, higher scores mean worse outcome.
Functional outcome (Quick Disability of Arm, Shoulder, Hand)
Evaluation of shoulder function using Quick Disability of Arm, Shoulder, Hand (Quick DASH) ranging from 0 (no disability) to 100 (most severe disability).
Quality of life in the patient with breast cancer (1)
Evaluation of quality of life using Functional Assessment of Cancer Therapy - Breast Cancer (FACT-B) The total FACT-B score ranges from 0 to 123, and is calculated by adding the scores from each of these subscales. Lower scores indicate better health.
Quality of life in the patient with breast cancer (2)
Evaluation of quality of life using EQ-5D-5L. This scale is numbered from -0.066 to 0.904. lower value means the worst quality of life you can imagine.

Full Information

First Posted
March 18, 2020
Last Updated
December 14, 2021
Sponsor
Samsung Medical Center
Collaborators
Ministry of Health, Republic of Korea
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1. Study Identification

Unique Protocol Identification Number
NCT04316156
Brief Title
Real-time Interactive Digital Healthcare System in Patients With Breast Cancer; Randomized Controlled Trial
Official Title
Hospital-home Linkage Short-term Rehabilitation Therapy Using Real-time Interactive Digital Healthcare System in Patients With Breast Cancer; Randomized Controlled Trial, Assessor Blinding, Multi-center Study
Study Type
Interventional

2. Study Status

Record Verification Date
December 2021
Overall Recruitment Status
Completed
Study Start Date
April 1, 2020 (Actual)
Primary Completion Date
November 17, 2021 (Actual)
Study Completion Date
November 17, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Samsung Medical Center
Collaborators
Ministry of Health, Republic of Korea

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
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 study. 100 breast cancer patients who underwent axillary lymph node diessection or breast reconstruction following 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.
Detailed Description
The limited range of motion (ROM) of the shoulder occur often after receiving breast cancer surgery, which may be due to post-operative pain, stiffness of shoulder girdle muscle, and etc. Due to this limited ROM, the patients may have difficulty with activities of daily life and quality of life may be reduced. Uincare Homeplus is software manufactured in Korea, which uses infrared, kinect camera and motion capture technology to track 3D motion of the patients' articulation. Using this technology, the patients can receive feedback of their motion immediately. The objective of the study is 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Range of motion
Allocation
Randomized
Enrollment
100 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exercise using Uincare Homeplus
Arm Type
Experimental
Arm Description
Uincare Homeplus
Arm Title
Exercise using brochure
Arm Type
Active Comparator
Arm Description
brochure
Intervention Type
Device
Intervention Name(s)
Uincare Homeplus
Other Intervention Name(s)
digital healthcare
Intervention Description
Interactive digital healthcare system
Intervention Type
Other
Intervention Name(s)
Brochure
Intervention Description
Brochure
Primary Outcome Measure Information:
Title
Range of motion in affected shoulder
Description
Evaluation of change in range of motion of the affected shoulder from baseline to 12 weeks
Time Frame
Enrollment, 4 week, 8 week, 12 week
Secondary Outcome Measure Information:
Title
Numerical rating scale of affected shoulder
Description
Evaluation of pain in the affected shoulder using numerical rating scale minimum ~ maximum value: 0 ~ 10, higher scores mean worse outcome.
Time Frame
Enrollment, 4 week, 8 week, 12 week
Title
Functional outcome (Quick Disability of Arm, Shoulder, Hand)
Description
Evaluation of shoulder function using Quick Disability of Arm, Shoulder, Hand (Quick DASH) ranging from 0 (no disability) to 100 (most severe disability).
Time Frame
Enrollment, 4 week, 8 week, 12 week
Title
Quality of life in the patient with breast cancer (1)
Description
Evaluation of quality of life using Functional Assessment of Cancer Therapy - Breast Cancer (FACT-B) The total FACT-B score ranges from 0 to 123, and is calculated by adding the scores from each of these subscales. Lower scores indicate better health.
Time Frame
Enrollment, 4 week, 8 week, 12 week
Title
Quality of life in the patient with breast cancer (2)
Description
Evaluation of quality of life using EQ-5D-5L. This scale is numbered from -0.066 to 0.904. lower value means the worst quality of life you can imagine.
Time Frame
Enrollment, 4 week, 8 week, 12 week

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients who underwent breast cancer surgery (axillary lymph node dissection or breast reconstruction following 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 and limited ROM before breast cancer surgery Those unable to perform exercise due to general deconditioning Those with communication difficulty
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
JIHYE HWANG, Professor
Organizational Affiliation
Physical & Rehabilitation Medicine Samsung Medical Center
Official's Role
Study Chair
Facility Information:
Facility Name
Samsung Medical Center
City
Seoul
State/Province
Gangnam-gu
ZIP/Postal Code
06351
Country
Korea, Republic of
Facility Name
Department of rehabilitation, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea
City
Seoul
State/Province
Seocho-gu
ZIP/Postal Code
06591
Country
Korea, Republic of

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
34412658
Citation
Park HY, Nam KE, Lim JY, Yeo SM, In Lee J, Hwang JH. Real-time interactive digital healthcare system for post-operative breast cancer patients: study protocol for a randomized controlled trial. Trials. 2021 Aug 19;22(1):549. doi: 10.1186/s13063-021-05535-8.
Results Reference
derived

Learn more about this trial

Real-time Interactive Digital Healthcare System in Patients With Breast Cancer; Randomized Controlled Trial

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