Additional Effects of Dry Needling With Conventional Physical Therapy Versus Conventional Physical Therapy in Plantar Fasciitis: a Randomized Control Trial

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-35
SponsorFoundation University Islamabad

About this trial

This study is a randomized controlled trial and the purpose of this study is to determine the effects of dry needling with conventional physical therapy versus conventional physical therapy on gait parameters in plantar fasciitis: a randomized control trial.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 40-60 years

Both genders

Plantar heel pain for longer than 3 months

Pain score at least or less than 8 on the numeric pain (NPRS)

Disqualifiers

Positive ankle drawer tests

Pregnant womwn, mental illness, immune suppressed patients, thrombocytopenia, anti-coagulant therapy patients and post-mastectomy

Congenital abnormalities of foot

A history of surgery to the ankle, foot or lower leg

Trial design

Design model

Parallel

Treatments tested in this trial

  • Standard treatment

    Procedure/Surgery

    All participants received up to six treatment sessions at a frequency of twice per week over a 3-week period i.e. ultrasound (0.5 W/cm² of 3 MHz for 5 minutes over plantar aspect of foot), stretching exercises and strengthening exercises. The exercise pro

  • Sham Dry needling

    Procedure/Surgery

    The sham dry needling group will also receive 6 sessions of sham dry needling on soleus, quadratus plantae, flexor digitorum brevis, and abductor halluces muscles for 5 minutes.Sterilized disposable stainless steel acupuncture needles of 0.25mm x 30mm will be used with depth of 20-55mm.The plantar and medial surface of the foot and ankle will be cleaned with alcohol. The sham dry needling will be performed for 5 minutes.

  • Dry needling

    Procedure/Surgery

    The dry needling group will receive 6 sessions of dry needling using a standardized trigger point protocol on soleus, quadratus plantae, flexor digitorum brevis, and abductor halluces muscles for 5 minutes. Sterilized disposable stainless steel acupuncture needles of 0.25mm x 30mm will be used with depth of 20-55mm. The calf, plantar and medial surface of the foot and ankle will be cleaned with alcohol. Following insertion, needles will be manipulated bi-directionally to elicit a sensation of aching, tingling, deep pressure, heaviness or warmth. The needles will then left in situ for 5 minutes.

Treatment groups

44 Participants
are divided into 2 treatment groups
Group A: Standard treatment + Sham Dry needlingActive comparator 2 interventions
Group B: Standard treatment + Dry needlingExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Pain intensity

Pain will be measured on Numerical Pain rating scale. The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine" or "worst pain imaginable").

Time frame
3 weeks
2

The Foot and Ankle Ability Measure (FAAM)

It is a self-report outcome instrument developed to assess physical function for individuals with foot and ankle related impairments .The response to each item on the ADL subscale is scored from 4 to 0, with 4 being 'no difficulty' and 0 being 'unable to do'

Time frame
3 weeks
3

Gait speed:

Gait speed = Distance (m) / time (s)

Time frame
3 weeks
4

Cadence

Cadence (steps/min) = steps counted x 60 / time (s)

Time frame
3 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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