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Extending Contingency Management's Benefits With Progressively Increasing Variable Interval Prize Reinforcement

Primary Purpose

Exercise, Addictive Behaviors

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
VIP CM
Sponsored by
UConn Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Exercise

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • age > 18 years
  • currently not physically active
  • Physically able and willing to walk 10,000 steps per day

Exclusion Criteria:

  • psychiatric or physical illness that could interfere with participation

Sites / Locations

  • UConn Heatlh Center

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

(A) Non-contingent control

VIP CM

Arm Description

Participants assigned to the control condition will be told to wear the pedometer daily and select a twice-weekly meeting schedule with research staff for 12 weeks (study weeks 4-15). On days randomly selected as meeting days, participants will be asked to bring in their pedometers. Participants who attend their scheduled meetings will receive a $5 gift card just for attending and bringing the pedometer, so long as it has registered steps walked in at least the past 4 days. They will be congratulated if they walked 10,000 steps or more on the prior 4 days, and encouraged to walk 10,000 steps or more per day on subsequent days.

Participants assigned to Increasing Variable Interval Prize (VIP) Reinforcement group will be scheduled for the same study visits as those in the Control group, but will also earn chances to win prizes if they have walked more than 10,000 steps in the past 4 days.

Outcomes

Primary Outcome Measures

number of steps walked in seven days prior to follow up assessment, as verified by the pedometer
number of steps walked in seven days prior to follow up assessment, as verified by the pedometer

Secondary Outcome Measures

Full Information

First Posted
August 10, 2010
Last Updated
April 5, 2019
Sponsor
UConn Health
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT01184040
Brief Title
Extending Contingency Management's Benefits With Progressively Increasing Variable Interval Prize Reinforcement
Official Title
Extending Contingency Management's Benefits With Progressively Increasing Variable Interval Prize Reinforcement
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
March 2012 (Actual)
Study Completion Date
March 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
UConn Health
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Exercise, Addictive Behaviors

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
61 (Actual)

8. Arms, Groups, and Interventions

Arm Title
(A) Non-contingent control
Arm Type
No Intervention
Arm Description
Participants assigned to the control condition will be told to wear the pedometer daily and select a twice-weekly meeting schedule with research staff for 12 weeks (study weeks 4-15). On days randomly selected as meeting days, participants will be asked to bring in their pedometers. Participants who attend their scheduled meetings will receive a $5 gift card just for attending and bringing the pedometer, so long as it has registered steps walked in at least the past 4 days. They will be congratulated if they walked 10,000 steps or more on the prior 4 days, and encouraged to walk 10,000 steps or more per day on subsequent days.
Arm Title
VIP CM
Arm Type
Experimental
Arm Description
Participants assigned to Increasing Variable Interval Prize (VIP) Reinforcement group will be scheduled for the same study visits as those in the Control group, but will also earn chances to win prizes if they have walked more than 10,000 steps in the past 4 days.
Intervention Type
Behavioral
Intervention Name(s)
VIP CM
Intervention Description
Participants will receive progressively increasing CM for walking 10,000 steps per day over 4 days prior to visit as verified by the pedometer.
Primary Outcome Measure Information:
Title
number of steps walked in seven days prior to follow up assessment, as verified by the pedometer
Time Frame
week 15
Title
number of steps walked in seven days prior to follow up assessment, as verified by the pedometer
Time Frame
week 24

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: age > 18 years currently not physically active Physically able and willing to walk 10,000 steps per day Exclusion Criteria: psychiatric or physical illness that could interfere with participation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Nancy M Petry, Ph.D.
Organizational Affiliation
UConn Health
Official's Role
Principal Investigator
Facility Information:
Facility Name
UConn Heatlh Center
City
Farmington
State/Province
Connecticut
ZIP/Postal Code
06030-3944
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Extending Contingency Management's Benefits With Progressively Increasing Variable Interval Prize Reinforcement

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