RECRUITING

To Improve Depressive Symptoms Using a Web-App

Conditions

Quick Navigation

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 being done to answer a question on whether a Web App-based Lifestyle Physical Activity Promotion Program is effective in improving depressive symptom experience of midlife Korean American women (WPAPP-K).

Official Title

A Web-App Based Lifestyle Physical Activity Promotion Program to Improve Depressive Symptom Experience: Midlife Korean American Women

Quick Facts

Study Start:2022-12-12

Study Completion:2026-10

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT05405803

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:40 Years to 60 Years

Sexes Eligible for Study:FEMALE

Accepts Healthy Volunteers:No

Standard Ages:ADULT

Inclusion Criteria	Exclusion Criteria
* self-reported midlife Korean-American women * aged 40 to 60 years * whose parents and grandparents are of Korean descent; * who can read and write English or Korean; * who currently reside in the United States; * who are sedentary (without any disabilities preventing physical activity); * who are online through computers or mobile devices; * have experienced depressive symptoms during the past two weeks (1 to 10 on the Patient Health Questionnaire \[PHQ-9\],which is equivalent to the cut-point of minimal to moderate depression.	* major signs or symptoms suggestive of pulmonary or CVD * history of a myocardial infarction, stroke, or Type I diabetes mellitus * blood pressure higher than 160/100 mm Hg * Use of beta-blockers, diltiazem, or verapamil

Inclusion Criteria

Exclusion Criteria

* self-reported midlife Korean-American women
* aged 40 to 60 years
* whose parents and grandparents are of Korean descent;
* who can read and write English or Korean;
* who currently reside in the United States;
* who are sedentary (without any disabilities preventing physical activity);
* who are online through computers or mobile devices;
* have experienced depressive symptoms during the past two weeks (1 to 10 on the Patient Health Questionnaire \[PHQ-9\],which is equivalent to the cut-point of minimal to moderate depression.

* major signs or symptoms suggestive of pulmonary or CVD
* history of a myocardial infarction, stroke, or Type I diabetes mellitus
* blood pressure higher than 160/100 mm Hg
* Use of beta-blockers, diltiazem, or verapamil

Contacts and Locations

Study Contact

Wonshik Chee, PhD

CONTACT

512-232-2121

wpapp.help@austin.utexas.edu

Principal Investigator

Eun-Ok Im, PhD, MPH

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, PhD, MPH, 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 Date2022-12-12

Study Completion Date2026-10

Study Record Updates

Study Start Date2022-12-12

Study Completion Date2026-10

Terms related to this study

Keywords Provided by Researchers

Depression
Korean american women

Additional Relevant MeSH Terms

Depression