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COMPLETED Phase 2

Contingency Management to Promote Weight Loss in Low Income Adults

NCT00875199 · View on ClinicalTrials.gov ↗

Study Summary

This study is designed to evaluate the feasibility and provide preliminary evidence for efficacy of a 12-week contingency management intervention to promote weight loss in overweight and obese low income adults in a community-based clinic. The study has three primary goals: (a) to determine if the contingency management treatment can be effectively applied to a new application, weight loss; (b) to obtain preliminary evidence for contingency management's efficacy in promoting weight loss and improving treatment retention, diet quality, physical activity levels, and self efficacy; and (c) to identify barriers and challenges to implementing contingency management for weight loss among low income patients.

Conditions Studied

Interventions

  • BEHAVIORAL contingency management
  • BEHAVIORAL weight loss manual-guided individual therapy sessions

Study Locations (1)

Connecticut

  • University of Connecticut Health Center — Farmington

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2009-03
Est. Completion 2010-03
Phase Phase 2

Sponsor

UConn Health

176 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00875199

The ClinicalTrials.gov registry entry for NCT00875199 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 30 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is UConn Health, which has 176 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Overweight appearing as the primary indexed condition, and to 2 interventions — of which contingency management is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT00875199 reports 1 study location spanning 1 distinct geographic area — top geographies include Connecticut. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT00875199 about?

NCT00875199 is a clinical study titled "Contingency Management to Promote Weight Loss in Low Income Adults". This study is designed to evaluate the feasibility and provide preliminary evidence for efficacy of a 12-week contingency management intervention to promote weight loss in overweight and obese low income adults in a community-based clinic. The study has three primary goals: (a) to determine if the c...

What is the current status of trial NCT00875199?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 30 participants. The study started on 2009-03. Estimated completion is 2010-03.

What conditions does trial NCT00875199 study?

This clinical trial studies the following conditions: Overweight. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00875199?

The interventions under investigation include: contingency management (BEHAVIORAL), weight loss manual-guided individual therapy sessions (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00875199?

This trial is sponsored by UConn Health, which has 176 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00875199 being conducted?

This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial