- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01305902
Substance Use and Fitness
April 5, 2019 updated by: UConn Health
Substance Use and Fitness: A Pilot Study of Contingency Management in Older Adults
The purpose of this pilot study is to estimate the effect size of a contingency management procedure that reinforces walking at rates consistent with the American College of Sports Medicine recommendations of 10,000 or more steps per day in older adults.
We expect that participants randomized to the contingency management intervention will increase walking to a greater degree than those assigned to a standard care condition.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
45
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Connecticut
-
Farmington, Connecticut, United States, 06030
- University of Connecticut Health Center
-
-
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.
Eligibility Criteria
Ages Eligible for Study
55 years to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- age 55 - 75 years
- currently not physically active
- willing and physically able as determined by physician approval to walk 10,000 steps per day
- blood pressure of 120-159 mmHg systolic or 80-99 mmHg diastolic
- willing to meet with research staff weekly for 12 weeks
Exclusion Criteria:
- psychiatric or physical illness that could interfere with participation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: walking recommendations
Participants assigned to this condition will be instructed to wear a pedometer daily and scheduled for weekly meetings over for the next 12 weeks.
Each week, they will be congratulated if they walked the target goal on any days, and encouraged to meet the goals for the upcoming week.
However, they will not receive any tangible reinforcement for walking.
The meetings will be brief (about 15 minutes) and will include discussions and handouts related to the health benefits of walking.
|
|
|
Experimental: contingency management for walking
Participants assigned to this condition will be asked to wear a pedometer daily and scheduled for weekly meetings over for the next 12 weeks.
The meeting duration and structure will be similar to that in the standard treatment condition including the handouts, with one exception.
Participants in this condition will earn tangible reinforcement in the form of prizes for walking the target number of steps per day.
|
Participants assigned to the experimental group will earn chances to win prizes if they have walked the recommended number of steps.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
number of days on which participants walked the recommended number of steps
Time Frame: Weeks 1-12
|
Weeks 1-12
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Nancy M Petry, Ph.D., University of Conncecticut Health Center
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 Major Dates
Study Start
January 1, 2011
Primary Completion (Actual)
April 1, 2012
Study Completion (Actual)
April 1, 2012
Study Registration Dates
First Submitted
February 25, 2011
First Submitted That Met QC Criteria
February 28, 2011
First Posted (Estimate)
March 1, 2011
Study Record Updates
Last Update Posted (Actual)
April 9, 2019
Last Update Submitted That Met QC Criteria
April 5, 2019
Last Verified
April 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 11-040-2
- P30DA023918 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Exercise
-
Centre Hospitalier de CorbieRecruitingExercise Training | Cardiac Rehabilitation | Exercise Intolerance | Exercise Intervention | Exercise Adaptations | HFrEF - Heart Failure With Reduced Ejection FractionFrance
-
Bitlis Eren UniversityCompletedExercise Physiology | Exercise ImmunologyTurkey (Türkiye)
-
Hamza KucukCompletedExercise Training | Exercise PhysiologyTurkey (Türkiye)
-
Faculdade de Motricidade HumanaCompletedGreen Exercise | Indoor ExercisePortugal
-
Lindenwood UniversityIncrenovo, LLCRecruitingCognitive Function | Blood Flow | Nitric Oxide | Endurance Exercise | Exercise Performance | Exercise RecoveryUnited States
-
Egas Moniz - Cooperativa de Ensino Superior, CRLCompletedAgeing | Aerobic Exercise | Resistance Exercise | Combined ExercisePortugal
-
Universidad Rey Juan CarlosCompletedEndurance Exercise | Running Performance | Exercise PhysiologySpain
-
Istanbul Sabahattin Zaim UniversityT.C. Dumlupınar ÜniversitesiCompletedExercise Ergogenics | Recovery Methods | Carnitine Ingestion | Exercise Fatigue | Exercise and RecoveryTurkey (Türkiye)
-
Hasan Kalyoncu UniversityNot yet recruiting
-
University of HawaiiKlein Buendel, Inc.CompletedMomZing Exercise Videos Online | Standard Exercise DVDUnited States
Clinical Trials on contingency management
-
VA Office of Research and DevelopmentActive, not recruitingPTSD | Cannabis-Related DisorderUnited States
-
Yale UniversityNational Institute on Drug Abuse (NIDA)Not yet recruiting
-
University of California, Los AngelesCompleted
-
Johns Hopkins UniversityJohns Hopkins Community PhysiciansWithdrawnSubstance-related DisorderUnited States
-
William StoopsNational Institute on Drug Abuse (NIDA)RecruitingMethamphetamine Use DisorderUnited States
-
Douglas Mental Health University InstituteRecruitingPsychotic Disorders | Cognitive Dysfunction | Cannabis Dependence | Cannabis Use | Memory Impairment | Schizophrenia; Psychosis | Cannabis Use Disorder | NeuroimagingCanada
-
University of Colorado, DenverUniversity of Colorado, BoulderEnrolling by invitation
-
UConn HealthNational Institute on Drug Abuse (NIDA)CompletedSubstance AbuseUnited States
-
Assiut UniversityNot yet recruitingOpioid Use Disorder (OUD)
-
UConn HealthNational Institute on Drug Abuse (NIDA)Completed