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NCT01184040 · ClinicalTrials.gov registry record · NA
Extending Contingency Management's Benefits With Progressively Increasing Variable Interval Prize Reinforcement
A NA study of Exercise and Addictive Behaviors, sponsored by UConn Health.
- Completed
- Registry status
- NA
- Development phase
- 61
- Enrollment target
- 1
- Study location
NCT01184040 is a NA study of Exercise and Addictive Behaviors that has completed, run by UConn Health. The registered enrollment target is 61 participants, below the 8,910-participant average among 57 other Exercise trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01184040, a NA study of Exercise and Addictive Behaviors, has completed, sponsored by UConn Health.
- COMPLETED
- Registry status
- NA
- Development phase
- 61 participants
- Enrollment target
- 1
- Study location
Study Summary
Contingency Management (CM) is highly effective in promoting recovery from substance use disorders, but benefits tend to attenuate over time when CM is discontinued. Identifying modifications of CM delivery that can extend its benefits is an important goal. The goal of this study is to evaluate the use of reinforcements to increase physical activity, specifically walking. The study provides a standard CM intervention to promote walking for three weeks. After three weeks, a progressively increasing variable interval schedule of reinforcement will be evaluated for increasing the durability of effects of the initial CM intervention. We hypothesize that Variable Interval Prize Contingency Management will result in greater adherence to a walking goal of 10,000 steps per day at Week 15 and Week 24 compared to the Control Condition.
Conditions Studied
Interventions
- BEHAVIORAL VIP CM
Study Locations (1)
Connecticut
- UConn Heatlh Center - Farmington
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 61 participants |
| Start Date | 2010-05 |
| Est. Completion | 2012-03 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01184040
The ClinicalTrials.gov registry entry for NCT01184040 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 61 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 8,910-participant average among 57 other Exercise trials with a reported enrollment target (99% lower). The listed sponsor is UConn Health, which has 178 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Exercise appearing as the primary indexed condition, and to 1 intervention - of which VIP CM is the first listed.
NCT01184040 reports 1 study location spanning 1 distinct geographic area - top geographies include Connecticut.
Frequently Asked Questions
What is clinical trial NCT01184040 about?
NCT01184040 is a clinical study titled "Extending Contingency Management's Benefits With Progressively Increasing Variable Interval Prize Reinforcement". Contingency Management (CM) is highly effective in promoting recovery from substance use disorders, but benefits tend to attenuate over time when CM is discontinued. Identifying modifications of CM delivery that can extend its benefits is an important goal. The goal of this study is to evaluate the ...
What is the current status of trial NCT01184040?
This trial is currently completed. It is a NA study. The enrollment target is 61 participants. The study started on 2010-05. Estimated completion is 2012-03.
What conditions does trial NCT01184040 study?
This clinical trial studies the following conditions: Exercise, Addictive Behaviors.
What interventions are being tested in trial NCT01184040?
The interventions under investigation include: VIP CM (BEHAVIORAL).
Who is sponsoring clinical trial NCT01184040?
This trial is sponsored by UConn Health, which has 178 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01184040 being conducted?
This trial has 1 study location across Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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