Plantar Fascitis Clinical Trial
— FRAMESOfficial title:
The Effects of Foot Rehabilitation And Minimalist Shoes (FRAMES) on Pain, Strength, and Function in Adults With Plantar Fasciopathy
The goal of this clinical trial is to compare the effects of 8 weeks of foot rehabilitation exercises in conjunction with wearing minimalist shoes in individuals with plantar fasciopathy, compared to only performing foot rehabilitation exercises. The main questions it aims to answer are: - Will individuals with plantar fasciopathy be able to reduce their pain and improve their self-reported function by performing rehabilitation exercises and wearing minimalist shoes, compared to those only performing rehabilitation exercises? - Will individuals with plantar fasciopathy be able to increase their intrinsic foot muscle strength and size, their balance, and gait biomechanics by performing rehabilitation exercises and wearing minimalist shoes, compared to those only performing rehabilitation exercises? - What characteristics of individuals with plantar fasciopathy make them most suited to succeed in a protocol of performing rehabilitation exercises and wearing minimalist shoes? Participants will be asked to come into the lab at the start of the intervention and after 8 weeks, where the following will be assessed: - Patient-reported outcomes - Foot morphology - Intrinsic foot muscle strength - Balance - Gait biomechanics For the intervention, participants in both groups will perform the same rehabilitation exercises, including: - Massage to the bottom of the foot - Calf-raises - Calf and foot stretches
Status | Recruiting |
Enrollment | 34 |
Est. completion date | May 20, 2025 |
Est. primary completion date | April 20, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 55 Years |
Eligibility | Inclusion Criteria: - Between ages of 18 - 55 years old - First-step pain in the morning over past week - Visual Analog Score between 30-70 mm - Heel pain for at least a month with an insidious onset Exclusion Criteria: - Other current lower extremity neuromusculoskeletal injury - Other lower extremity neuromusculoskeletal injuries other than the foot in the past 3 months - Previous history of foot/ankle fractures or surgeries - Current participation in formal rehab for plantar fasciopathy - Previous minimalist shoe experience |
Country | Name | City | State |
---|---|---|---|
United States | University of Virginia | Charlottesville | Virginia |
Lead Sponsor | Collaborator |
---|---|
University of Virginia |
United States,
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in Pain | Visual Analog Scale (0-100 mm) pain outcome scores for the following items:
Average pain over the past week First-step pain over the past week (the pain that is felt upon waking up in the morning and taking a first step) Average heel pain of the day |
This outcome change will be measured from baseline, to the midpoint of the intervention (4 weeks), to the end of the intervention (8 weeks) for both groups. | |
Primary | Change in perception of overall recovery | Global Rating of Change (GROC) outcome scores | This outcome change will be measured from baseline, to the midpoint of the intervention (4 weeks), to the end of the intervention (8 weeks) for both groups. | |
Primary | Change in self-reported function and health | Foot Health Status Questionnaire (FHSQ) outcome scores | This outcome change will be measured from baseline, to the midpoint of the intervention (4 weeks), to the end of the intervention (8 weeks) for both groups. | |
Primary | Change in foot morphology: length, width, arch height, and girth | Arch Height Index tool outcome measures | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Primary | Change in intrinsic foot muscle size | Muscle thickness and cross-sectional area of the abductor hallucis, flexor hallucis brevis, flexor digitorum brevis, and quadratus plantae, using diagnostic ultrasound in a weight-bearing position. | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Primary | Change in intrinsic foot muscle strength | Tested separately for the great toe and lesser toes using two different types of handheld dynamometer | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Primary | Change in center of pressure (COP) distance during balance | COP distance using a force plate during a single-limb balance task, eyes open and eyes closed. | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Primary | Change in foot posture outcomes | Clinical foot posture index assessment (23-point scale) | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Primary | Change in center of pressure (COP) velocity during balance | COP velocity using a force plate during a single-limb balance task, eyes open and eyes closed. | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Primary | Change in center of pressure (COP) 95% ellipse area during balance | COP 95% ellipse area using a force plate during a single-limb balance task, eyes open and eyes closed. | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Primary | Change in vertical ground reaction force (vGRF) of the rearfoot | The force (N) during treadmill and overground walking using loadsol sensors | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Secondary | Change in kinesiophobia | Tampa Scale of Kinesiophobia (TSK-11) outcome scores | This outcome change will be measured from baseline, to the midpoint of the intervention (4 weeks), to the end of the intervention (8 weeks) for both groups. | |
Secondary | Change in fear-avoidance belief | Fear-Avoidance Belief Questionnaire (FABQ) outcome scores | This outcome change will be measured from baseline, to the midpoint of the intervention (4 weeks), to the end of the intervention (8 weeks) for both groups. | |
Secondary | Change in pain self-efficacy | Pain Self-Efficacy Questionnaire (PSEQ) outcome scores | This outcome change will be measured from baseline, to the midpoint of the intervention (4 weeks), to the end of the intervention (8 weeks) for both groups. | |
Secondary | Change in activity level | National Aeronautics and Space Administration Activity Survey (NAS) | This outcome change will be measured from baseline, to the midpoint of the intervention (4 weeks), to the end of the intervention (8 weeks) for both groups. | |
Secondary | Change in vertical ground reaction force (vGRF) of the whole foot | The force (N) during treadmill and overground walking using loadsol sensors | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Secondary | Change in vertical ground reaction force (vGRF) of the midfoot | The force (N) during treadmill and overground walking using loadsol sensors | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Secondary | Change in vertical ground reaction force (vGRF) of the forefoot | The force (N) during treadmill and overground walking using loadsol sensors | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Secondary | Change in average loading rate | The loading rate (N/s) during treadmill and overground walking using loadsol sensors | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Secondary | Change in instantaneous loading rate | The loading rate (N/s) during treadmill and overground walking using loadsol sensors | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Secondary | Change in knee sagittal plane kinematics | Knee sagittal plane joint moment (in Nm/kg) measured during the overground gait analysis using markerless motion capture | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Secondary | Change in hip sagittal plane kinematics | Hip sagittal plane joint moment (in Nm/kg) measured during the overground gait analysis using markerless motion capture | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Secondary | Change in ankle sagittal plane kinematics | Ankle sagittal plane joint moment (in Nm/kg) measured during the overground gait analysis using markerless motion capture | This outcome change will be measured from baseline, to the end of the intervention (8 weeks) for both groups. | |
Secondary | Change in steps per day | Steps per day measured on a Fitbit | This outcome change will be measured everyday for 8 weeks | |
Secondary | Change in activity level per day | Hours of activity per day measured on a Fitbit | This outcome change will be measured everyday for 8 weeks |
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