Use a Wearable Devices to Observe Complications of Mobilization for Colorectal Cancer After Surgery

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

192 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-08-08

Study Completion Date

2024-01-08

Brief Summary

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This study aims to help patients recover faster after colorectal cancer surgery by using wearable devices to monitor early movement.

Patients will wear a lightweight wristband that tracks heart rate, sleep, and daily steps after surgery. The goal is to find out if early walking can reduce the chances of complications, shorten hospital stays, and lower medical costs.

Participants will start wearing the device after surgery and continue for about 7 days or until they leave the hospital. During this time, they will also fill out a simple daily observation form. Participation is voluntary, and patients can withdraw at any time without affecting their care.

The study hopes to provide new ways to improve recovery and offer better support to patients after colorectal surgery.

Detailed Description

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Conditions

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Colorectal Cancer

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Postoperative Colorectal Cancer Patients with Wearable Device Monitoring

Patients diagnosed with colorectal cancer who underwent minimally invasive surgery. Participants wore a wrist-worn device to monitor postoperative physical activity, heart rate, and sleep for up to 7 days or until discharge.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

1. Patients undergoing minimally invasive colorectal tumor resection.
2. Aged 20 to 85 years.
3. ECOG score 0-2.
4. Clear consciousness and ability to communicate in Mandarin or Taiwanese (or via family translation).
5. Informed consent provided by the patient or family.

Exclusion Criteria

1. Patients with acute/chronic psychiatric disorders or cognitive impairment.
2. Patients undergoing traditional open or local resection surgeries.

Minimum Eligible Age

20 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Responsible Party

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Responsibility Role SPONSOR

Locations

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Chang Gung Memorial Hospital, Linkou

Taoyuan District, , Taiwan

Site Status

Countries

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Taiwan

Other Identifiers

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CMRPG3M2171

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

202102412B0

Identifier Type: -

Identifier Source: org_study_id