Effect of Orthopedic Blocking on Cervical Spine Flexion and Extension Strength
NCT ID: NCT00758888
Last Updated: 2009-07-24
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.
UNKNOWN
NA
30 participants
INTERVENTIONAL
2008-09-30
2008-10-31
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.
Sacroiliac Orthopedic Blocking and Cervical Spine Function
NCT00523822
Feasibility Study of Short-Term Effects of Chiropractic Manipulation on Older Adults With Impaired Balance
NCT00497510
Effects of Cervical Manipulation on Cervical Rotation Motion and Shoulder Rotational Motion and Strength in Overhead Athletes
NCT06903793
Chiropractic Distraction Spinal Manipulation- Lumbar Stenosis Study
NCT03863769
Cervical Spine Manipulation Affects on Balance and Proprioception
NCT01745705
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.
Treatment
Place the blocks under the pelvis for 2 minutes
Orthopedic Blocking
Place the blocks under the pelvis for 2 minutes
Trochanter Belt
Participant is fitted with trochanter belt on the adjusting table and wear it while Investigator checks their flexion and extension strength.
Trochanter Belt
Participant is fitted with trochanter belt on the adjusting table and wear it while Investigator checks their flexion and extension strength.
Sham
Participant lies on adjusting table, blocks are placed in a similar configuration but distant to actual points of leverage.
Blocking Sham
Participant lies on adjusting table, blocks are placed in a similar configuration but distant to actual points of leverage.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Orthopedic Blocking
Place the blocks under the pelvis for 2 minutes
Trochanter Belt
Participant is fitted with trochanter belt on the adjusting table and wear it while Investigator checks their flexion and extension strength.
Blocking Sham
Participant lies on adjusting table, blocks are placed in a similar configuration but distant to actual points of leverage.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Tumors
* Myopathies
* Consumption of prescription drugs that affect nervous system function
* Recent cervical spine injuries or surgeries
* Cervical pain
18 Years
30 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Logan College of Chiropractic
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Logan College of Chiropractic
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Logan College of Chiropractic
Chesterfield, Missouri, United States
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
RD0801080145
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.