Impact of Brief Daily Functional Resistance Training on Lower Extremity Physical Performance (FASTNIA)
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Estimated)
Enrollment
Phase
Phase
- Phase 2
- Phase 3
Contacts and Locations
Study Contact
Study Contact
- Name: Christopher Sciamanna, MD, MPH
- Phone Number: 610-585-9765
- Email: cns10@psu.edu
Study Contact Backup
- Name: Jordan Kurth, Ph.SD.
- Phone Number: 815-988-6357
- Email: jkurth@pennstatehealth.psu.edu
Study Locations
-
-
Pennsylvania
-
Hershey, Pennsylvania, United States, 17033
- Recruiting
- Penn State College of Medicine
-
Contact:
- Christopher N Sciamanna, MD, MPH
- Phone Number: 610-585-9765
- Email: csciamanna@pennstatehealth.psu.edu
-
Contact:
- Jordan D Kurth, PhD
- Email: jkurth@pennstatehealth.psu.edu
-
Principal Investigator:
- Christopher N Sciamanna, MD
-
Pittsburgh, Pennsylvania, United States, 15261
- Recruiting
- University of Pittsburgh
-
Contact:
- Bonny Rockette-Wagner, PhD
- Phone Number: 412-624-0188
- Email: bjr26@pitt.edu
-
Principal Investigator:
- Bonny Rockette-Wagner, PhD
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Self-reported difficulty or inability to walk ¼ mile
Exclusion Criteria:
- Chest pain on the PAR-Q
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Experimental: Functional Activity Strength TRaining
Participants will perform 5 minutes of functional resistance training daily, supported by 24 video coaching sessions over 12 months.
|
FAST consists of five exercises (stepping on a step, chair stands, push-ups, rows, walking), for 30 seconds each, performed daily, with 30 seconds of rest between.
|
|
Active Comparator: Delayed Treatment
Participants will receive the intervention after 12 months.
|
FAST consists of five exercises (stepping on a step, chair stands, push-ups, rows, walking), for 30 seconds each, performed daily, with 30 seconds of rest between.
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Short Physical Performance Battery
Time Frame: Baseline, 6 months, 12 months
|
The SPPB assesses balance, gait speed, and lower extremity strength.
|
Baseline, 6 months, 12 months
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Investigators
Investigators
- Study Chair: Maggie Nellissery, Ph.D., National Institute on Aging (NIA)
Study record dates
Study Major Dates
Study Start (Actual)
Study Start
Primary Completion (Estimated)
Primary Completion
Study Completion (Estimated)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Actual)
First Posted
Study Record Updates
Last Update Posted (Actual)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
Other Study ID Numbers
- STUDY00024492
- R01AG079938 (U.S. NIH Grant/Contract)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
- ICF
- CSR
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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.
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