RECRUITING

Cancer Pain Management Using a Web-based Intervention

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Cancer Pain Management: A Technology-Based Intervention for Asian American Breast Cancer Survivors

Quick Facts

Study Start:2024-02-20
Study Completion:2027-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06085313

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * women aged 18 years and older who identify as Chinese, Korean, or Japanese;
  2. * have had a breast cancer diagnosis in the past;
  3. * can read and write English, Mandarin (simplified or traditional), Korean, or Japanese;
  4. * have access to the internet through computers or mobile devices (mobile phones and tablets);
  5. * have experienced cancer pain during the past week (at least 1 on a scale from 0 to 5 \[no symptom=0, mild symptom that does not bother=1, somewhat bothering symptom=2, moderate symptom=3, severe symptom=4, and worst possible symptom=5\]);
  6. * have experienced depressive symptoms during the past two weeks (1 to 10 on the Patient Health Questionnaire) which is equivalent to the cut-point of minimal to moderate depression.
  1. * less than 18 years old because their cancer experience would be different from that of adults.
  2. * Those who are in treatment or not in treatment, but who were diagnosed with breast cancer within the past five years, will be excluded.
  3. * Those who participated in the PI's pilot studies will be excluded.
  4. * The participants of R33 phase will exclude those in active depression treatment regardless of their level of depression.
  5. * Those without Internet access will be excluded, but those with Internet access through community/group computers will be included.

Contacts and Locations

Study Contact

Wonshik Chee
CONTACT
512-232-2142
cai.help@austin.utexas.edu
OVPR
CONTACT
512-471-2877
research@utexas.edu

Principal Investigator

Eun Ok Im
PRINCIPAL_INVESTIGATOR
The University of Texas at Austin

Study Locations (Sites)

The University of Texas at Austin
Austin, Texas, 78712
United States

Collaborators and Investigators

Sponsor: University of Texas at Austin

  • Eun Ok Im, PRINCIPAL_INVESTIGATOR, The University of Texas at Austin

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-02-20
Study Completion Date2027-08-31

Study Record Updates

Study Start Date2024-02-20
Study Completion Date2027-08-31

Terms related to this study

Additional Relevant MeSH Terms

  • Cancer of Breast
  • Depressive Symptoms
  • Cancer Pain