Telemedicine Improves Pain-related Disabilities in Following up Cancer Pain Outpatient

Mahidol University

Status: Enrolling

Conditions: Cancer Pain; Pain, Chronic

Treatments: Other: Telemedicine; Other: In-person

Study type: Interventional

Funder types: Other

Identifiers

NCT05628246

Si 310/2022

Details and patient eligibility

About

Cancer is the second leading cause of death worldwide, with approximately 18.1 million new cases and 9.6 million deaths reported in 2018. Cancer-related pain is experienced by 50-70% of patients, with a higher prevalence at advanced disease stages (66.4%). Since the development of WHO's cancer pain guidelines, several studies have reported good relief of symptoms and suffering for a majority of patients. Recent reports suggest that up to 50% of patients still report insufficient pain control. Patients with cancer often present with multiple symptoms and functional decline. Evidence supports multidisciplinary approaches to address symptoms and suffering, including early palliative care referral

From review literatures we found that the telemedicine group had significantly higher quality of life than the usual care group. In addition, the telemedicine group had lower anxiety and depression scores than the usual care group.

Therefore, we will conduct the non-randomized controlled study of using telemedicine comparing to conventional in-person at OPD in hospitalized cancer pain patients.

The purpose of this study is to assess the pain interference by using the Brief Pain Inventory (BPI) and to compare between the in-person group and the telemedicine group. To assess the cost-effectiveness of telemedicine for reducing symptoms associated with cancer and its treatment.

Full description

The pain interference will be assessed and compared using Brief Pain Inventory from 0-70 between In-person group and telemedicine group at 1 month.

Enrollment: 206 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age older than 18 years old
• Cancer patients who new visit as out patient at pain clinic, Siriraj hospital

Exclusion criteria

• Cannot read and write
• Confusion
• Unable to use the 0-10 Numerical Rating Scale (NRS) to rate pain intensity.
• Unstable clinical presentation

Trial design

Primary purpose: Health Services Research

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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206 participants in 2 patient groups

In-person

Active Comparator group

Description:

Face to face at OPD

Treatment:

Other: In-person

Telemedicine

Experimental group

Description:

Telemedicine

Treatment:

Other: Telemedicine