Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06231199
Other study ID # P.T.REC/012/004276
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date January 25, 2024
Est. completion date April 25, 2024

Study information

Verified date January 2024
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

this study will be conducted to investigate the efficacy of combining foam roller and gastrocnemius release on pain intensity level, dorsi flexion range of motion of ankle joint ,dorsi flexion range of motion of big toe and foot function in subjects with plantar fasciitis.


Description:

Plantar fasciitis refers to degeneration and inflammation of the proximal plantar fascia. The condition presents with plantar medial heel pain, often exacerbated following periods of inactivity, such as upon waking in the morning.The term "plantar fasciitis" has been quoted for years, but this is a misnomer as inflammatory cells are not present in biopsies from involved fascia. Therefore, advocate the terminology "plantar fasciitis" to explain the syndrome characterized by pain along the proximal plantar fascia and its attachment in the area of the calcaneal tuberosity with function impairment, implying a more chronic degenerative process than acute heel pain.Research found that both stretching and foam rolling techniques helped reduce pain and increase the ROM. However, the effectiveness of foam rolling was superior to stretching in terms of increased pressure pain thresholds (PPTs) at gastrocnemius and soleus. there was a gap in the previous literature in combined effect of gastrocnemius release and foam roller in managing plantar fasciitis and assessing dorsi flexion range of motion of both big toe and ankle joint along with pain assessment and foot function. sixty patients with planter fascitis will be assigned randomly to two groups; first one will receive manual and foam roller release of gastrocnemius and conventional treatment and the other one will receive conventional treatment only.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 60
Est. completion date April 25, 2024
Est. primary completion date April 25, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - aged between 18 years and 60 years - heel pain in the morning with first step, insidious sharp pain under the heel, tenderness on medial calcaneus and symptoms decreasing with slight activity (like walking) and worsening toward the end of the day Exclusion Criteria: - Infective conditions of foot, tumor, calcaneal fracture - Metal implant around ankle - Dermatitis, acute sepsis and anesthetic areas - Subject with impaired circulation to lower extremities - Subject with referred pain due to sciatica - Corticosteroids - Injection in heel preceding 3 month - Patient who cannot co-operate - history of flat foot

Study Design


Related Conditions & MeSH terms


Intervention

Other:
gastrocnemius release
The patient will be prone to lying and the therapist will stand at the side of the patient's leg. The therapist uses both hands in cross-hand pattern (Figure 10a and 10b). Myofascial Release will be performed for 20 repetitions, then gastrocnemius release by foam roller;This involved long sitting, with the affected leg will be extended on the foam roller and foot relaxed. The non-affected leg will be flexed at knee so that the foot will be rested on the floor. The participants will be instructed to use their arms and non_affected foot to propel their body back and forth from the popliteal fossa to Achilles tendon in continuous motion. then patients perform plantar fascia realise from standing by foam roller
conventional treatment
the patients will receive conventional treatment in the form of ultrasound therapy (continuous mode/1MHZ) followed by plantar fascia stretch and inctruction

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary pain intensity level visual analogue scale will be used for assess pain intensity level. VAS was a 10-cm-long horizontal line with no pain and worst possible pain at the extremes of the line up to four weeks
Primary ankle dorsiflexion Electro goniometers are electronic versions of the standard goniometers used in the clinic to measure ankle dorsiflexion ROM up to four weeks
Primary foot function The foot function index (questionnaire) will be used to assess foot function. it consists of 23 self-reported items divided into 3 subcategories based on patient values: pain, disability and activity limitation. The patient has to score each question on a scale from 0 (no pain or difficulty) to 10 (worst pain imaginable or so difficult it requires help) up to four weeks
Secondary big toe range of motion Electro goniometers are electronic versions of the standard goniometers used in the clinic to measure big toe range of motion up to four weeks
See also
  Status Clinical Trial Phase
Completed NCT05071365 - Early Access to Virtual Resources for the Self-management of Plantar Fasciitis N/A
Not yet recruiting NCT05479500 - Investigation of the Efficacy of Myofascial Chain Release Techniques on Plantar Fasciitis N/A
Not yet recruiting NCT05479526 - Effect of The Superficial Back Line on the Development of Plantar Fasciitis
Recruiting NCT04423900 - Smart Phone-Based Application for Evaluation and Rehabilitation of HindFoot Pain N/A
Completed NCT04204824 - Ultrasound Treatment in the Management of Plantar Fasciitis N/A
Completed NCT04162262 - Effects of Exercise Versus Exercise and Instrument-Assisted Soft Tissue Mobilization for Plantar Fasciopathy Treatment N/A
Completed NCT03246087 - Acupuncture for Plantar Fasciosis in the Primary Care Setting N/A
Completed NCT05647291 - Is ESWT Better in Plantar Fasciitis Treatment? N/A
Withdrawn NCT03873207 - Offloading Device for Post Surgical Foot Procedures N/A
Completed NCT05347264 - Comparative Effects of Gun Massager and Transverse Friction Massage in Patients With Plantar Fasciitis N/A
Recruiting NCT04175288 - The Effectiveness of Ultrasound Treatment in the Management of Plantar Fasciitis N/A
Completed NCT03731897 - Evaluation of the Efficacy of Prolotherapy Treatment in Patients With Plantar Fasciitis: a Randomized Double-blind Study N/A
Recruiting NCT05462002 - Intrinsic Foot Muscle Morphology and Function in Runners With and Without Plantar Fasciitis
Active, not recruiting NCT06466616 - Shock Waves Combined With Leg Stretches in Patients With Plantar Fasciitis N/A
Completed NCT05207592 - Urdu Version of Foot and Ankle Disability Index: A Reliability and Validity Study
Not yet recruiting NCT06394336 - Early Intervention With Therapeutic Exercise in Plantar Fasciopathy N/A
Completed NCT05867888 - Shock Wave Therapy Versus Low Level Laser Therapy in Patients With Plantar Fasciitis N/A
Completed NCT06023836 - Myofascial Pain Syndrome and Plantar Fasciitis Treatment N/A
Completed NCT05856019 - Effects of J Stroke Myofascial Release in Patients With Planter Fasciitis N/A
Completed NCT06446167 - Comparative Efficacy of Laser, Extracorporeal Shockwave Therapy and Exercise Therapy on Plantar Fasciitis Outcomes N/A