Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
574 participants
OBSERVATIONAL
2009-08-31
2011-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
The primary objective of this study is to identify the factors associated with awareness and utilization of discount generic prescription programs and how two low-income populations in Houston utilize the $4 for a 30-day supply or $10 for a 90-day supply, Generic Prescriptions Program offered by Kroger, Randalls, Target, Walmart, HEB, CVS, and Walgreens.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Patient-Directed Lifestyle Change and Health Promotion Program or Usual Care in Low-Income, Uninsured Participants in Los Angeles County, California
NCT00521209
Improving Health Habits in Impoverished Populations
NCT00569595
Social Determinants and a Diabetes Prevention Program Tailored for African Americans
NCT05301413
A Prescription for Health Equity: A Healthcare Provider-based Produce Prescription Program for People With Prediabetes and Type 2 Diabetes
NCT05939349
Grocery Prescription Program for Medicaid Adults With Hypertension or Type 2 Diabetes
NCT06033664
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
During the focus group, you will complete a form that asks for basic demographic information (such as your age and sex).
The focus group discussions will be taped, and the recorded tapes will be transcribed word-for-word. The taped recording of the focus group study will be stored in a safe and secured locker by the study chair. The taped recordings will be destroyed after 5 years.
Length of Study:
Your participation on this study will end once you complete the focus group.
This is an investigational study.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
CASE_ONLY
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Low-income Populations
Survey
20 minute survey to determine the relationship between awareness of the discount generic prescription program and utilization of the program.
Focus Group
5 - 8 focus groups of 6 - 10 people, lasting approximately 90 minutes
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Survey
20 minute survey to determine the relationship between awareness of the discount generic prescription program and utilization of the program.
Focus Group
5 - 8 focus groups of 6 - 10 people, lasting approximately 90 minutes
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Low-income (less than $30,000/year)
* Ability to speak English
* Ability to read and write in English
* Chronic health condition requiring prescription medication or family member with chronic health condition requiring prescription medication.
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
M.D. Anderson Cancer Center
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Lovell A. Jones, PHD, BS, MA
Role: STUDY_CHAIR
UT MD Anderson Cancer Center
Anthony Omojasola, DRPH
Role: PRINCIPAL_INVESTIGATOR
UT MD Anderson Cancer Center
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Independence Heights Community Health Center
Houston, Texas, United States
HOPE Clinic
Houston, Texas, United States
Second Mile Mission Center
Houston, Texas, United States
Countries
Review the countries where the study has at least one active or historical site.
Related Links
Access external resources that provide additional context or updates about the study.
UT MD Anderson Cancer Center website
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2009-0340
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.