The Effect of Osteopathic Manual Therapy on Vascular Supply

NCT ID: NCT01020591

Last Updated: 2017-05-04

Study Results

Results available

Outcome measurements, participant flow, baseline characteristics, and adverse events have been published for this study.

View full results

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-12-31

Study Completion Date

2010-03-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to determine if the use of osteopathic manual therapy can influence the vascular supply to the knee, knee range of motion, balance and knee pain, in a group of subjects with knee osteoarthritis. It is also the objective of this study to determine if there is a difference between the osteopathic evaluation and the combination of an osteopathic evaluation and treatment.

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.

Knee Osteoarthritis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Osteopathic evaluation

osteopathic evaluation of motion and tissue mobility

Group Type ACTIVE_COMPARATOR

Osteopathic evaluation

Intervention Type OTHER

evaluation of movement and tissue mobility

Osteopathic evaluation with treatment

osteopathic evaluation of motion and tissue mobility followed by osteopathic manual therapy release of the tight or restricted tissues

Group Type EXPERIMENTAL

Osteopathic evaluation with treatment

Intervention Type OTHER

osteopathic evaluation followed by osteopathic manual therapy release of tissues identified as tight or restricted

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Osteopathic evaluation

evaluation of movement and tissue mobility

Intervention Type OTHER

Osteopathic evaluation with treatment

osteopathic evaluation followed by osteopathic manual therapy release of tissues identified as tight or restricted

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Radiographic-confirmed knee osteoarthritis

Exclusion Criteria

* Subjects who are unable to ambulate independently (without an aid) and safely the distance of a city block
* Subjects who have an uncontrolled medical condition (e.g. heart (angina) or respiratory condition (asthma))
* Subjects who have a neurological condition (e.g. Parkinson's, Multiple Sclerosis)
* Subjects who have both knees affected by osteoarthritis and have had previous surgery to both knees
* Subjects who have knee OA in only one knee and that knee has had previous knee surgery
* Subjects who have previous vascular surgery to either leg
Minimum Eligible Age

50 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Nova Scotia Health Authority

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Wendy Jardine

Physiotherapist osteopath

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Wendy M Jardine, MScPT

Role: PRINCIPAL_INVESTIGATOR

Nova Scotia Health Authority

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Capital District Health Authority

Halifax, Nova Scotia, Canada

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Canada

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

CDHA-RS/2010-227

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Resistance Training in Knee Osteoarthritis
NCT01099371 UNKNOWN PHASE2/PHASE3