Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06085313

Cancer Pain Management Using a Web-based Intervention

Led by University of Texas at Austin · Updated on 2025-09-15

300

Participants Needed

1

Research Sites

184 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study is funded by the HEAL Initiative (https://heal.nih.gov/). Based on Preliminary Studies (PSs), the research team developed and pilot-tested an evidence-based Web App-based information and coaching/support program for cancer pain management (CAPA) that was culturally tailored to Asian American breast cancer survivors using multiple unique features. However, CAPA rarely considered depressive symptoms accompanying pain in its design or components, and PSs indicated the necessity of further individualization of the intervention components of CAPA due to diversities in the needs of ABD. The purpose of the proposed 2-phase study is to further develop CAPA with additional components for ABD and the individual optimization functionality (CAI) and to test the efficacy of CAI in improving cancer pain experience of ABD. The specific aims are to: a) develop and evaluate CAI through an expert review and a usability test (R61 phase); b) determine whether the intervention group (that uses CAI and usual care) will show significantly greater improvements than the active control group (that uses CAPA and usual care) in primary outcomes (cancer pain management and cancer pain experience including depressive symptoms) from baseline to post 1-month and post 3-months; c) identify theory-based variables (attitudes, self-efficacy, perceived barriers, and social influences) that mediate the intervention effects of CAI on the primary outcomes; and d) determine whether the effects of CAI on the primary outcomes are moderated by selected background, disease, genetic, and situational factors. This study is guided by the Bandura's Theory and the stress and coping framework by Lazarus and Folkman. The R61 phase includes: (a) the intervention development process, (b) a usability test among 15 ABD, 15 family members, and 15 community gatekeepers; and (c) an expert review among 10 experts in oncology. The R33 phase adopts a randomized repeated measures control group design among 300 ABD. Long-term goals are: (a) to extend and test CAI in various healthcare settings with diverse subgroups of ABD, (b) examine the costeffectiveness, sustainability, and scalability of CAI in the settings, and (c) translate CAI into health care for ABD.

CONDITIONS

Official Title

Cancer Pain Management Using a Web-based Intervention

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Women aged 18 years and older who identify as Chinese, Korean, or Japanese
  • Have had a breast cancer diagnosis in the past
  • Can read and write English, Mandarin (simplified or traditional), Korean, or Japanese
  • Have access to the internet through computers or mobile devices
  • Experienced cancer pain during the past week (at least mild pain on a 0 to 5 scale)
  • Experienced depressive symptoms during the past two weeks (minimal to moderate depression on the Patient Health Questionnaire)
Not Eligible

You will not qualify if you...

  • Younger than 18 years old
  • Diagnosed with breast cancer within the past five years, whether currently in treatment or not
  • Participated in the principal investigator's pilot studies
  • Receiving active depression treatment during the R33 phase
  • No internet access (though access through community or group computers is allowed)

AI-Screening

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Trial Site Locations

Total: 1 location

1

The University of Texas at Austin

Austin, Texas, United States, 78712

Actively Recruiting

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Research Team

W

Wonshik Chee

CONTACT

O

OVPR

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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