Comparing the Effectiveness of Various Interventions on Improving Lumbar Proprioception
NCT ID: NCT04712695
Last Updated: 2021-01-19
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
80 participants
INTERVENTIONAL
2020-02-03
2020-11-10
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
-For the seated forward flexion test, the participants' C7 and S2 vertebrae were identified and used as markers. The participants were asked to bend forward until the tape measure increased 5 cm from the original distance between the C7 and S2 vertebrae. Similar to the seated flexion test, during the side-bending task, the participants were asked to side bend until the tip of their middle finger was 10 cm closer to the floor. The participants were asked to memorize that point in their mind; they were then blindfolded and asked to repeat the movement 10 times, trying to recreate the original position to the best of their ability.
Between initial and final measurements of proprioception, the participants were randomly assigned to one of the following four groups for interventions for a 10-minute training session:
* Graded Motor Imagery Group: Participants were shown several flashcards with pictures of individuals' back oriented to either the flexed or side bent position. The participants stated which direction the image depicted and visualized themselves making the movement identified in the picture.
* Mirror Visual Feedback Group:
Participants viewed themselves in a mirror while performing flexion and side bending movements.
-Augmented Biofeedback Group: Participants used an augmented musculoskeletal feedback system smartphone application app and small sensors with Bluetooth technology to translate the movement of the participant into an avatar on the game.
-Diaphragmatic Breathing Group: Participants were told to sit on a chair with their back straight and feet flat on the floor with one hand on their chest and one hand on their stomach. They performed diaphragmatic breathing in a slow 4 second box method: breathing in for 4 seconds, holding for 4 seconds, breathing out for 4 seconds, and then hold for 4 seconds
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
The Effects of Proprioceptive Neuromuscular Facilitation Training
NCT04178356
Postural Control and Trunk Neuromuscular Activation in Athletes With Chronic Low Back Pain
NCT02969785
The Back Exercises to Neutralize Disability Study
NCT02308189
Influence of Physical Activity Level on Lumbar Movement Control
NCT05649150
Proprioceptive Training and Low Back Pain
NCT01505595
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
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Graded Motor Imagery Group
Exercise Based Interventions
Proprioception Training Interventions
Mirror Visual Feedback Group
Exercise Based Interventions
Proprioception Training Interventions
Augmented Biofeedback Group
Exercise Based Interventions
Proprioception Training Interventions
Diaphragmatic Breathing Group
Exercise Based Interventions
Proprioception Training Interventions
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Exercise Based Interventions
Proprioception Training Interventions
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Must be able to perform low intensity exercise
Exclusion Criteria
* Back pain within the past 6 months
* Musculoskeletal injury within the past 6 months
18 Years
35 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Black Hills State University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Craig Triplett
Associate Professor Exercise Science
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Black Hills State University
Spearfish, South Dakota, 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.
BlackHillsSU
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.