Effect of Graston Technique on Planter Thickness in Patients With Planter Fasciitis
PF
1 other identifier
interventional
50
0 countries
N/A
Brief Summary
this study will be conducted to investigate the effect of Graston Technique on Planter Thickness in Patients With Planter Fasciitis
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 Feb 2024
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 31, 2024
CompletedFirst Posted
Study publicly available on registry
February 8, 2024
CompletedStudy Start
First participant enrolled
February 10, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2024
CompletedFebruary 8, 2024
January 1, 2024
3 months
January 31, 2024
January 31, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
plantar thickness
Ultrasonography will be used to measure planter thickness
up to six weeks
Secondary Outcomes (4)
pain intensity
up to six weeks
pain intensity at the first step
up to six weeks
functional levels of foot
up to six weeks
pain pressure threshold
up to six weeks
Study Arms (2)
Garston technique
EXPERIMENTALthe patients will receive graston technique with exercise program three times aweek for six weeks
exercise program
ACTIVE COMPARATORthe patients will receive an exercise program three times a week for six weeks
Interventions
the patients will receive instrumented assisted soft tissue mobilization using the Graston technique, which includes the application of a cream to the posterior calf and plantar foot from the knee to the toes to reduce friction on the skin. The Graston tools will be used to mobilize the tissues of the triceps surae and plantar foot bypassing the tools along the leg and foot
the patients will receive pedaling an exercise bicycle for 5 min with minimal resistance to warm the tissues, gastrocnemius stretches performed on a step for three repetitions held for 30 sec each , plantar fascia stretching performed in a seated position for three repetitions held for 30 sec each, and foot intrinsic muscular strengthening using a short foot exercise. Ice will be offered as needed for pain management after each session in addition to home program exercise
Eligibility Criteria
You may qualify if:
- patients that Clinically diagnosed cases of plantar fasciitis not less than 6 weeks.
- patients willing to precipitate in the study and take treatment for 6 successive weeks.
- Heel pain felt maximally over the plantar aspect of heel
- Pain in the heel on the first step in the morning
- No history of rest pain in the heel
You may not qualify if:
- Subjects with clinical disorders where therapeutic ultrasound is contraindicated such as infective conditions of foot, tumor, calcaneal fracture, metal implant around ankle.
- Subjects with a clinical disorder where myofascial release is contraindicated as dermatitis.
- Subjects with impaired circulation to lower extremities
- Subjects with referred pain due to sciatica and other neurological disorders.
- Arthritis
- Corticosteroids injection in heel preceding 3 months
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Masking Details
- opaque sealed envelop
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principle investigator nabil mahmoud ismail abdel-aal
Study Record Dates
First Submitted
January 31, 2024
First Posted
February 8, 2024
Study Start
February 10, 2024
Primary Completion
April 30, 2024
Study Completion
April 30, 2024
Last Updated
February 8, 2024
Record last verified: 2024-01