Manual Therapy and Rehabilitation on Pain and Physical Functioning for Chronic Knee Pain
NCT ID: NCT04880954
Last Updated: 2021-07-15
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
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UNKNOWN
NA
36 participants
INTERVENTIONAL
2021-03-31
2023-03-31
Brief Summary
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Participation will include 2 assessment days and a 12-week treatment cycle. Assessments will be conducted during week 1 and after treatment. The treatment will vary based on the assigned group. This may include 12 in-person manual therapy sessions occurring once per week and or 12-weeks of at-home therapy occurring 5 times per week.
The greatest risk of participation includes possible muscle/joint soreness, injury during at-home exercises, and loss of confidentiality.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Soft Tissue Mobilization
Soft Tissue Mobilization
Soft Tissue Mobilization will be provided to participants by Licensed Chiropractor focusing on structures of the lower and upper leg. This will be provided for 20 minutes, once per week for 12 weeks.
Rehabilitation
Rehabilitation
Participants will engage in 20 minutes of prescribed at-home exercise 5 times per week, for 12 weeks.
Soft Tissue Mobilization and Rehabiliation
Soft Tissue Mobilization
Soft Tissue Mobilization will be provided to participants by Licensed Chiropractor focusing on structures of the lower and upper leg. This will be provided for 20 minutes, once per week for 12 weeks.
Rehabilitation
Participants will engage in 20 minutes of prescribed at-home exercise 5 times per week, for 12 weeks.
Interventions
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Soft Tissue Mobilization
Soft Tissue Mobilization will be provided to participants by Licensed Chiropractor focusing on structures of the lower and upper leg. This will be provided for 20 minutes, once per week for 12 weeks.
Rehabilitation
Participants will engage in 20 minutes of prescribed at-home exercise 5 times per week, for 12 weeks.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
Yes
Sponsors
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Neuro Performance Integration
OTHER
Responsible Party
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Beverly Albert
Research Director
Principal Investigators
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Beverly Albert, MS
Role: PRINCIPAL_INVESTIGATOR
Neuro Performance Integration
Locations
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Neuro Performance Integration
Park City, Utah, United States
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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#21-NPI-101
Identifier Type: -
Identifier Source: org_study_id
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