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A Pilot Tele-rehabilitation Trial for Breast Cancer Survivors

A Pilot Feasibility Study of a Tele-rehabilitation System Among Women Who Undergo a Unilateral Mastectomy for Breast Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04269967
Enrollment
40
Registered
2020-02-17
Start date
2020-11-01
Completion date
2022-12-31
Last updated
2022-09-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer Female

Brief summary

Breast cancer is the leading cancer affecting women in Singapore. Breast cancer survivors commonly experience declined physical function and quality of life, due to their upper limb morbidity and wound issues post-surgery. Rehabilitation therapy can address the aforementioned issues that the survivors may experience during their recovery. No therapy however, can be effective if patients do not utilize them. Home-based telehealth (e.g., tele-rehabilitation) self-managed by patients and guided by healthcare professionals can potentially improve the service use and recovery. This study aims to understand the lived experience of post-mastectomy tele-rehabilitation and recovery process among female patients who undergo a unilateral mastectomy for breast cancer.

Interventions

OTHERReceiving routine rehabilitation care via tele-rehabilitation system

Drain care education, self-massage techniques and exercise (PT and OT)

Sponsors

Singapore General Hospital
CollaboratorOTHER
National Cancer Centre, Singapore
CollaboratorOTHER
National University of Singapore
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
21 Years to 99 Years
Healthy volunteers
No

Inclusion criteria

* Female 21 years and over * Underwent a recent unilateral breast surgery (wide excision or simple mastectomy) with lymph nodes removed * Speak and write English or Mandarin; * No psychiatric history or chronic psychiatric condition as assessed by referring clinician

Exclusion criteria

* Having breast reconstruction * Having legal blindness or severe visual impairment * Having life expectancy of less than three months (12- weeks) * Having previous upper limb injury or conditions that limit passive ranges of shoulder flexion (\<150°), elbow extension/flexion (0/145°)

Design outcomes

Primary

MeasureTime frameDescription
The experience of rehabilitation (i.e., drain care, exercise and massage)12 weeks from the baseline assessmentWe will interview our participants about their experience of going through a rehabilitation process. This is qualitative data.
Shoulder range of motionPre rehabilitation (week 0) and post-rehabilitation (week 12)Shoulder ranger of motion will be measured in degree.
Arm circumferencePre rehabilitation (week 0) and post-rehabilitation (week 12)Arm circumference will be measured in cm

Countries

Singapore

Contacts

Primary ContactMiho Asano
epham@nus.edu.sg6565166929

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 16, 2026