Purpose

This is a feasibility pilot test of a single-arm intervention to evaluate the beta version of an mHealth app-based behavioral intervention prior to scaling for a randomized controlled trial (RCT). This mHealth intervention is designed to enhance self-efficacy and support pain and symptom self-management among post-treatment cancer survivors.

Conditions

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • In a post-treatment stage with no evidence of disease (complete remission) - Diagnosed with cancer in the past three years - Experiencing cancer/treatment-related pain - ≥ 18 years of age at the time of first diagnosis - Cognitively able to actively participate in an online-based study - Able to read, write, and understand English

Exclusion Criteria

  • Individuals who currently use any medication for psychiatric reasons (including stimulants, and mood stabilizers) - Patients with major psychotic disorders (bipolar disorder or schizophrenia) and/or substance use disorders. - Those who are currently pregnant or plan to become pregnant in the next three months

Study Design

Phase
N/A
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Primary Purpose
Supportive Care
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Mobile Health (mHealth) Intervention
Implement a bank of 60 mHealth intervention messages, ecological momentary assessments (EMAs), and e-diary entries to PiLR to deliver a 1-week mHealth intervention to cancer survivors experiencing pain
  • Behavioral: Mobile Health (mHealth) Intervention
    Individuals will use the mHealth app for 1 week. Participants will interact with evidence-based messages and will complete ecological momentary assessments (EMA's) (two times per day) and electronic diaries (e-diaries) daily.

Recruiting Locations

Virginia Commonwealth University
Richmond, Virginia 23298
Contact:
Sun Jung Kim, Ph.D
804-628-4688
sjkim2@vcu.edu

More Details

Status
Recruiting
Sponsor
Virginia Commonwealth University

Study Contact

Sun Jung Kim, Ph.D
804-628-4688
sjkim2@vcu.edu

Detailed Description

The intervention involves a set of tested intervention messages, ecological momentary assessments (EMAs), and e-diary entries to our PsyMINT mobile app. A 1-week mHealth intervention to cancer survivors who experience pain will be delivered. The feasibility of an mHealth app platform (PsyMINT) as a message presentation environment will be delivered and evaluated. The app messages will target five topics/modules, including psychoeducational materials related to pain management; positive psychology; opioid literacy; skill building for patient-provider communication and trust; and quality of life.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.