The Efficacy of Pain Management With Self-reporting Pain Monitoring System in Cancer Patient

DERSHENG SUN68 enrolled

Overview

To compare the pain scales between clinician evaluated and reported with wearable device by patients.

To compare the pain scales between clinician evaluated and reported with wearable device by patients with cancer of advanced stage.

Study Type

INTERVENTIONAL

Allocation

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

Conditions

Pain

Interventions

using device for scoring pain scale, named "ANAPA®"DEVICE

wearable device for scoring pain scale

Eligibility

Sex: ALLMin age: 20 Years

Medical Language ↔ Plain English

Inclusion Criteria: * over 20 year old * cancer pain with visual analog scale or numeric rating scale score \>/- 4 * opioids candidates * with informed consent form Exclusion Criteria: * life expectancy within 3 months

Locations (2)

Daejeon St. Mary's Hospital, the Catholic University of Korea

Daejeon, South Korea

Seoul St. Mary's Hospital, the Catholic University of Korea

Seoul, South Korea

Outcomes

Primary Outcomes

Actual difference of pain scales

comparing the pain scale assessed by wearable device and that assessed by physician when out patient clinic.

Time frame: 1 week after using wearable pain scale device - baseline and 1 week.

Central Contacts

DERSHENG SUN, MD, PhD

CONTACT

+82-31-820-3584 ds-sun@hanmail.net

HYESUNG WON, MD, PhD

CONTACT

+82-31-820-5247 woncomet@catholic.ac.kr

Data from ClinicalTrials.gov

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