Comparison of Ergon Instruments-Assisted Soft Tissue Mobilization With Compressive Myofascial Release
Study Comparing the Effectiveness of Ergon Instruments-Assisted Soft Tissue Mobilization Techniques With Compressive Myofascial Release for Plantar Fasciitis: A Randomised Clinical Trial
1 other identifier
interventional
60
1 country
1
Brief Summary
The objective of this study is to investigate the effects of Virtual Reality and Motor Imagery along with Routine Physical Therapy in motor function and balance in patients with Parkinson disease.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Mar 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2021
CompletedFirst Submitted
Initial submission to the registry
February 20, 2022
CompletedFirst Posted
Study publicly available on registry
February 28, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 25, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2022
CompletedJune 2, 2022
May 1, 2022
1.1 years
February 20, 2022
May 31, 2022
Conditions
Keywords
Outcome Measures
Primary Outcomes (4)
Range of Motion
Goniometer has been the most widely used tool for measuring joint range of motion. To ensure reliable measurement, standardized, specific positions and landmarks are used to measure each joint movement.
12th Week
Visual Analogue Scale
The Visual Analog Scale is a 10 cm line with anchor statements on the left, no pain and on the right, extreme pain.
12th Week
Foot and Ankle Disability Index
The Foot and Ankle Disability Index has 26 items. Each item is scored from 0; unable to do, to 4; no difficulty at all. The Foot and Ankle Disability Index has a total point value of 104 points.
12th Week
Foot and Ankle Ability Measure
The Foot and Ankle Ability Measure (FAAM) is a self-report outcome instrument/questionaire developed to assess physical function for individuals with foot and ankle related impairments. 8-item Sports Subscale. Each item is scored on a 5-point Likert scale (4 to 0) from 'no difficulty at all' to 'unable to do'. Item score totals, which range from 0 to 84 for the ADL subscale and 0 to 32 for the Sports subscale, were transformed to percentage scores. Higher scores represent higher levels of function for each subscale, with 100% representing no dysfunction.
12th Week
Study Arms (2)
Instrument-assisted Soft Tissue Mobilization
EXPERIMENTAL1. Warm-up will be performed for 10 to 15 minutes by light jogging, elliptical machine, stationary cycle or an upper body ergometer 2. Instrument-assisted Soft Tissue Mobilization , will be applied at 30 to 60 degrees angle for 40 to 120 seconds 3. Stretching, for 30 seconds (3 rep) 4. Strengthening exercises, high repetitions with low intensity exercise 5. Cryotherapy for 10 to 20 min
Compressive Myofascial Release Technique
EXPERIMENTALCompressive myofascial release technique will be applied 5 minutes, after a warmup of 10 to 15 minutes.
Interventions
Instrument-assisted soft tissue mobilization is used for a mechanical benefit for the therapist providing deeper approach and braces remodeling of connective tissues through dissolution of extravagant fibrosis, while provoking repair and reconstructing forwarded by the recruitment of fibroblast.
Compressive Myofascial Release Technique is a technique of soft tissue stretching that uses compression and sustained myofascial stretches to create a releasing force in the targeted area
Eligibility Criteria
You may qualify if:
- Inability to achieve 20 degrees of active dorsiflexion,
- Heel pain,
- Mid foot pain,
- Heal swelling,
- Mid foot swelling,
- Achilles' tendon tightness diagnosed on the base of Windlass test
You may not qualify if:
- Recent foot injury,
- Fracture,
- Infections,
- Surgical procedures,
- Tendon injury,
- Hypermobility,
- Neuromuscular disorders,
- Impaired sensation,
- Open sores,
- Skin disease,
- Active deep vein thrombosis or thrombophlebitis,
- Bruises,
- Varicose veins,
- Burn scars
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Ripah International University
Faisalabad, Punjab Province, 38000, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Muhammad Kashif
Riphah International University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- Our study will be single-blinded, outcome assessor-blinded. The assessor will be blinded to avoid being biased during the outcome assessment.
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
February 20, 2022
First Posted
February 28, 2022
Study Start
March 1, 2021
Primary Completion
March 25, 2022
Study Completion
March 31, 2022
Last Updated
June 2, 2022
Record last verified: 2022-05
Data Sharing
- IPD Sharing
- Will not share