MORE in the Management of Lumbosacral Radiculopathy Symptoms: A Randomized Controlled Trial
Last updated on July 2021Recruitment
- Recruitment Status
- Recruiting
- Estimated Enrollment
- Same as current
Summary
- Conditions
- Lumbar Radiculopathy
- Type
- Interventional
- Phase
- Not Applicable
- Design
- Allocation: RandomizedIntervention Model: Parallel AssignmentIntervention Model Description: Control Group = treatment as usual (TAU) Intervention Group = 8-week virtual mindfulness sessionMasking: Double (Investigator, Outcomes Assessor)Masking Description: RAs recruited onto the study team to conduct study visits will not have access to information regarding participant group assignment. Study leads providing the intervention will have the opportunity to run baseline participant visits but will not be allowed to run follow-up study visits for participants in any cohort to which they have delivered an intervention. The Principal Investigator and statistician will be completely blinded to group assignmentsPrimary Purpose: Treatment
Participation Requirements
- Age
- Between 18 years and 65 years
- Gender
- Both males and females
Description
Not Provided
Not Provided
Tracking Information
- NCT #
- NCT04818606
- Collaborators
- Not Provided
- Investigators
- Principal Investigator: Courtney "Katie" Pickworth, ND, MS National University of Natural Medicine