Plantar Fascitis Clinical Trial
Official title:
Smart Phone-Based Application for Evaluation and Rehabilitation of HindFoot Pain
This randomized controlled study aims to evaluate the status of the individuals with hindfoot pain and to recommend preventive precautions and appropriate exercise programs with Smart Phone-Based Applications. Additionally, to compare the results of patients who attended through mobile applications (Achilles Tendinopathy and Plantar Fasciitis) with the results of patients included in the hands-on program.
Status | Recruiting |
Enrollment | 120 |
Est. completion date | December 30, 2021 |
Est. primary completion date | September 1, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility |
Inclusion Criteria: - Pain in the heel and surrounding area - Have given consent to be a volunteer for participating to the study - 18 years and older - Ability to use a smartphone Exclusion Criteria: - Having foot and ankle injury and surgery in the last three months - Have received physiotherapy or local injection before randomization - Having major pathologies during the rehabilitation program (severe heart and neuropsychiatric disorders, complicated diabetes mellitus) - Neoplastic formation in the foot-ankle region - Vision problem - Night pain |
Country | Name | City | State |
---|---|---|---|
Turkey | Elif Tugçe Çil | Istanbul | Europe |
Lead Sponsor | Collaborator |
---|---|
Yeditepe University |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | The Victorian Institute of Sport Assessment-Achilles Questionnaire | The VISA-A aims to evaluate the clinical severity of patients with chronic Achilles tendinopathy. It can be used to determine the patient's clinical severity and provide a guideline for treatments as well as for monitoring the effect of treatment. Robinson et al. designed the Victorian Institute of Sports Assessment-Achilles (VISA-A) questionnaire, as a region-specific functional questionnaire, to assess the severity of AT.6 It contains eight questions that cover the three domains of pain (questions 1-3), function (questions 5-7) and activity (questions 7 and 8). Scores are summed to give a total out of 100. An asymptomatic person would score 100. It has proven to be a valid and reliable instrument to measure disability in cross-cultural studies conducted in Turkey | 8 weeks | |
Other | Foot Function Index | FFI assessed pain, activity restriction, and disability. The pain subscale, which includes nine items, measures foot pain related to a variety of conditions. Various functional activities depending on foot problems were determined by the disability subscale, which also includes nine items. Activity restrictions due to foot problems were assessed with an activity limitation subscale containing five items. Higher scores indicate more pain, disability, and limited activity. In our study, the patients were asked to mark each category with a score between 0 and 10 about their pain, activity restriction, and disability level. All the categorized scores were collected, and a total score was noted. | 8 weeks | |
Primary | Feiss Line test | Feiss Line is an ankle examination procedure that tests for pes planus, flatfoot, fallen medial longitundinal arch.Patient should be standing with weight distributed evenly. The examiner uses a marker to mark the inferior apex of medial malleolus and medial surface of the base of the base of the 1st metatarsal. The examiner draws a line connecting the two points. The examiner locates the the navicular tuberosity and marks it. |
8 weeks | |
Primary | the Range of Motion of the ankle | Physiotherapist will measure the Range of Motion of the ankle by using Goniometer | 8 weeks | |
Primary | Visual Analog Scale - Pain Assesment | Visual Analogue Scale (VAS) was used to estimate the severity of participants' first step (morning time) and activity pain. It consists of a line, usually 100 mm long, whose ends are labeled as the extremes (no pain and worst pain imaginable); the rest of the line is blank. | 8 weeks | |
Secondary | Tampa Scale for Kinesiophobia | Tampa consists of 17 questions and is used in diseases associated with acute and chronic low back pain, fibromyalgia, and musculoskeletal injuries. The scale uses a 4-point Likert score (1 = Strongly disagree, 4 = Strongly agree). A total score is calculated after the reversal of items 4, 8, 12, and 16. The patients can have a total score of between 17-68. The higher the score indicates, the higher the kinesiophobia | 8 weeks |
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