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OpenTrials
Completed

NCT Number: NCT05328700

Effectiveness of Neuromuscular Kinesiology Taping in Plantar Fasciitis

One of the pathologies most studied and treated with kinesiotape (KT) is plantar fasciitis (PF). In most of the studies reviewed, it is concluded that there is an improvement in the symptoms of PF when treated with KT: either combined with other therapies or as a single treatment compared to placebo. However, most current studies have limitations because the sample is small, the effect size is small, and the evidence is insufficient or of low quality.

In the present work, the aim is to study the effectiveness of KT in PF, and to compare the results with those obtained in a placebo group, which is treated with tape. The researchers will assess the decrease in symptoms prior to performing other definitive treatments. In addition, the variability of the painful symptoms and the durability of the bandage will be studied, in order to determine whether it can be used in the short or long period of time, being able to take it into account and supposing a supplement to the pharmacological treatment.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Universitat de València

Valencia, 46010, Spain

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • People with acute plantar fasciitis with less than 3 months of evolution
  • Who present pain in the fascia both during ambulation and on palpation
  • Ecographic image compatible with plantar fasciitis (> 4 mm)
  • The condition has not be previously treated with other treatment

Exclusion criteria

  • Condition with no sintomatology

Treatment and study plan

Kinesiotaping

Other

Perform a neuromuscular bandage with kinesiotape in patients with plantar fasciitis

Tape

Other

Perform a neuromuscular bandage with tape (Hipofix(R)) in patients with plantar fasciitis

Primary outcomes

  1. Visual Analogue Scale of Pain

    Time frame: Change from baseline (before intervention) to one day, two days, three days and four days after intervention

    A visual analogue scale of pain will assess from 0, no pain, to 10, the worst possible pain

Secondary outcomes

  1. Bandage durability

    Time frame: Change from baseline (the bandage is put on) until the first day that the loss of the bandage is documented, assessed up to 7 days

    Period of time in days from when the bandage is put on until it comes off

Sponsors and collaborators

Lead sponsor

University of Valencia

Other

Registry information

Important dates

Study start
2022
Primary completion
2022
Study completion
2022
First posted
Apr 14, 2022
Registry last updated
Nov 29, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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