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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03677167
Other study ID # MeuhedetHCO
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 29, 2018
Est. completion date August 31, 2020

Study information

Verified date December 2019
Source Meuhedet. Healthcare Organization
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Many patients suffer from chronic heel pain, and studies have not yet found the most appropriate treatment. There are some researchers who claim that the pain is caused by weakness in the muscles of the foot, which causes increased pressure in the heel. In walking, the muscles of the foot are activated and strengthened. No research has yet been done on whether walking (barefoot or with shoes) on a treadmill reduces pain in the heel and improves function.


Description:

A bare foot functions differently than a foot in a shoe while walking, as there are differences in movement, muscle tone, pressure and sensation. Wearing shoes over the years can cause changes in walking and pain. In the examination of the feet of patients suffering from chronic pain in the heel was found a smaller volume of muscle, and calcification in the heel area that could be caused by increased pressure. Although the trend of physiotherapy treatments has changed in recent years from passive to active treatments, the overwhelming majority of studies are testing passive therapies only as a treatment option for chronic heel pain. Barefoot walking has not been tested as an option for treating chronic pain in the heel, although there are studies indicating that bare feet lead to reduced heel pressure, increased muscle work, and better proprioception.The purpose of this study is to examine the effect of barefoot walking on the level of pain, function and pain threshold for stress in patients with chronic heel pain.


Recruitment information / eligibility

Status Completed
Enrollment 52
Est. completion date August 31, 2020
Est. primary completion date August 31, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Local pain in the heel that lasts more than 12 weeks,

- pain in the first steps in the morning

- Pain that disappears in situations of weightlessness

- Ability to walk on a moving track.

Exclusion Criteria:

- Pain in proximal areas along the leg or lower back pain that can radiate to the heel

- Sensory disorders for various reasons

- Tumors, fractures, previous operations in the lower extremities

- Irritable cardiovascular problems

- Balance problems and dizziness.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
walking on a treadmill
Patients will go on the treadmill (barefoot or with shoes) twice a week for a month, up to a medium-high level effort, and will receive ultrasound treatment for the painful heel spot

Locations

Country Name City State
Israel Meuhedet Health Care Phisiotherapy Clinic Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
Meuhedet. Healthcare Organization

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary change in results of sf-36 scale from baseline to 4 weeks of intervention and 8 weeks This is a questionnaire consisting of eight separate parts, each section examining a different aspect of quality of life. In the evaluation of pain in the heel, it is customary to use a part that assesses functional function, and in part that evaluates physical pain. The score ranges from 0 - very low, to 100 - very high. A change of 7.8 points indicates a change in the level of pain and physical function. before intervention, after 4 weeks of intervention, after 4 weeks from the end of intervention (i.e. baseline to 4 weeks of intervention and 8 weeks)
Secondary change in results of VAS pain in the heel that appears on the first step in the morning from baseline to 4 weeks and 8 weeks The ladder is 10 cm long, and the patient must surround the number that corresponds to his or her pain intensity, 0 - does not hurt at all, and 10 - the most severe and intolerable pain. When a change of 1.4 cm out of 10 cm indicates a change in the patient's pain level before intervention, after 4 weeks of intervention, after 4 weeks from the end of intervention (i.e. baseline to 4 weeks of intervention and 8 weeks)
Secondary change in results of Pain threshold severity for minimum pressure and tolerance threshold for pain for pressure at five points in the heel, from baseline to 4 weeks and 8 weeks The algometer will measure the intensity of the pressure at the point of pain until reaching the minimum pain (P1) and also until reaching the threshold of pain tolerance before intervention, after 4 weeks of intervention, after 4 weeks from the end of intervention (i.e. baseline to 4 weeks of intervention and 8 weeks)
Secondary change in results of Three clinical tests to diagnose chronic pain in the heel, from baseline to 4 weeks and 8 weeks Three clinical trials have been found to be relevant to the diagnosis of chronic heel pain. All the tests listed below are performed on the painful leg and until the first sensation of pain (p1) is produced:
Static standing on one leg: measuring the number of seconds (up to 20 sec) and the level of pain on a visual analog scale (VAS);
Crouching on one leg: measuring the number of repetitions (up to10 rep) and the level of pain according to VAS;
Ascension on fingertips: Measuring the number of repetitions (up to10 rep) and the level of pain according to VAS.
It was found that when pain is produced in one of the above tests, the patient may be diagnosed with chronic heel pain. The results options for all of the above tests are "positive" (if at least one of the tests creates pain) or "negative" (if non of the tests creates pain)
before intervention, after 4 weeks of intervention, after 4 weeks from the end of intervention (i.e. baseline to 4 weeks of intervention and 8 weeks)
Secondary change in the duration (minuets) of walking on the treadmill until reaching level 6 on the short borg scale,from base line to 4 weeks the duration of walking on the treadmill until reaching level 6 on the short borg scale. 1st intervention, after 4 weeks of intervention
Secondary change in the walking speed (Kilometer/hour) on the treadmill until reaching level 6 on the short borg scale,from baseline to 4 weeks change in the walking speed (Kilometer/hour) on the treadmill until reaching level 6 on the short borg scale 1st intervention, after 4 weeks of intervention
Secondary short borg scale The short borg scale is a scale that assesses the intensity of physical activity according to the subjective feeling of the patient. The short borg scale ranges from 0 - rest mode to 10 - maximum exertion.
Training at level 5-6 has been found to be effective in achieving physiological improvement.
1st intervention, after 4 weeks of intervention
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