Actively Recruiting

Phase Not Applicable
Age: 30Years - 65Years
FEMALE
NCT07414914

Self-Myofascial Release Plus Exercise Versus Exercise Alone in Type 2 Diabetes

Led by Izmir Katip Celebi University · Updated on 2026-02-17

40

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

Sponsors

I

Izmir Katip Celebi University

Lead Sponsor

C

Cigli Regional Training Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

This randomized controlled trial aims to investigate the effects of adding self-myofascial release applied to the plantar fascia and gastrosoleus muscles to an exercise program on foot function, physical performance, and plantar fascia thickness in individuals with type 2 diabetes. Participants aged 30 to 65 years with controlled type 2 diabetes will be randomly allocated to either an exercise-only group or an exercise plus self-myofascial release group. Both groups will complete an eight-week supervised exercise program three times per week. The intervention group will additionally perform self-myofascial release using a foam roller before exercise sessions. Outcomes will include foot function, balance, functional mobility, gait performance, and plantar fascia thickness assessed by ultrasonography before and after the intervention.

CONDITIONS

Official Title

Self-Myofascial Release Plus Exercise Versus Exercise Alone in Type 2 Diabetes

Who Can Participate

Age: 30Years - 65Years
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Individuals aged 30 to 65 years
  • Diagnosed with type 2 diabetes mellitus for at least 1 year
  • Controlled type 2 diabetes mellitus
  • Able to ambulate independently without assistive devices
Not Eligible

You will not qualify if you...

  • Severe pes planus or pes cavus defined by Foot Posture Index-6 (score  +10 or  -5)
  • History of plantar fasciitis
  • Plantar fascia ulceration
  • Peripheral neuropathy
  • Diagnosed peripheral vascular disease
  • History of lower extremity surgery or fracture during last year
  • Rheumatologic or connective tissue disorders affecting soft tissue
  • Neurological or diagnosed cognitive disorders
  • Pregnancy
  • Other types of diabetes mellitus
  • Obesity (BMI > 30 kg/m8)
  • Serious cardiopulmonary disorders, including heart failure, myocardial infarction history, or severe COPD or asthma

AI-Screening

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Trial Site Locations

Total: 1 location

1

Bakırçay University Çiğli Regional Education Hospital

Izmir, İzmir, Turkey (Türkiye), TR-35620

Actively Recruiting

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Research Team

S

Sümena HAREKET KARAKAYA, PT

CONTACT

M

Müge KIRMIZI, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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