Home-Based Functional Exercise Program in Patients With Patellar Femoral Syndrome Over a 10-Week Period
NCT ID: NCT03407365
Last Updated: 2019-01-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
11 participants
INTERVENTIONAL
2016-09-27
2018-08-27
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Comparing Rehabilitation Programs for Patellofemoral Pain Syndrome
NCT00445224
Comparison of Treatments Following Total Knee Replacement
NCT02237911
Effects of Contralateral Strength Training on Postoperative Strength Deficits in the Immobilized Lower Extremity
NCT03650374
Effects of Lumbopelvic Manipulation on Hip and Knee Neuromuscular Activity
NCT01637480
Ilium Mobilization in Patellofemoral Pain Syndrome Treatment
NCT05708495
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
CROSSOVER
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Home Exercises
Patients will be given a set of home exercises to perform as part of their rehabilitation home exercise program. They will be initially trained by a research team member and will be given a DVD home exercise video with instructions on how to perform the exercises.
10 Week Exercise Program
Subjects will complete a 10 week exercise program using DVD with instructions provided. Participants will have to do one session of exercise on 5 different days each week for a total of 5 sessions per week, for 10 weeks.
DVD Program
Weeks 1-10, subjects will not be prescribed exercise at home. If the DVD program shows to help participants in Group 1, the program and DVD will be provided to Group 2 participants
DVD Program After 10 Weeks
If the DVD program shows to help participants in Group 1, the program and DVD will be provided to Group 2 participants
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
10 Week Exercise Program
Subjects will complete a 10 week exercise program using DVD with instructions provided. Participants will have to do one session of exercise on 5 different days each week for a total of 5 sessions per week, for 10 weeks.
DVD Program After 10 Weeks
If the DVD program shows to help participants in Group 1, the program and DVD will be provided to Group 2 participants
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Subjects diagnosed with patella-femoral syndrome. We will ascertain this by asking a few questions, which will not be recorded as they have not been enrolled in the study yet.
* Capable of following and completing a 10 week home exercise program
Exclusion Criteria
* Individuals unable to participate, i.e. cognitive deficits, weakness or functional deficits to upper extremities.
* Individuals unable to tolerate exercise program
18 Years
50 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
NYU Langone Health
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Wayne Stokes, MD
Role: PRINCIPAL_INVESTIGATOR
NYU Langone Health
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
New York University School of Medicine
New York, New York, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
12-00210
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.