Evaluation Of Balance And Ankle Proprioception In Calcaneal Spur Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age40-60
SponsorCairo University

About this trial

this study will be conducted to investigate the difference in balance and ankle proprioception between calcaneus spur patients and age matched normal subjects

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

age will range from 40-60

both sex male and female

unilateral calcaneal spur

Patients with pain and inflammation at the bottom of heel, or the location where the spur is present.

Disqualifiers

Surgery within the last 6 months

Sensory or motor paralysis -Received steroid injections within the last 3 months-

discrepancy in length of the lower extremities greater than or equal to 1 cm.

systemic disease in the last six months that may predispose to heel pain(e.g., rheumatoid arthritis and lupus). (Dudoniene V et al.,2023).

Trial population

fifty two subjects will be assigned to two group; group with calcaneal spur and healthy group

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

Not listed

Trial groups

52 Participants
are grouped into 2 trial groups
Group A: calcaneal spur group
Group B: healthy group

Trial outcomes

Primary outcomes

1

dynamic balance

the Biodex Balance System (BBS) ,Version 3.1, has been used to evaluate postural balance

Time frame
up to one day
2

static balance

The single-leg stance balance test will be used to assess static balance.

Time frame
up to one day
3

ankle propriception

digital inclinometer will be used to assessed ankle proprioception

Time frame
up to one day
4

foot disability

A Foot Function Index (FFI) will be used to assess foot disability. The pain subcategory consists of 9 items and measures foot pain in different situations, such as walking barefoot versus walking with shoes. The disability subcategory consists of 9 items and measures difficulty performing various functional activities because of foot problems, such as difficulty climbing stairs. The activity limitation subcategory consists of 5 items and measures limitations in activities because of foot problems, such as staying in bed all day. Recorded on a visual analogue scale (VAS), scores range from 0 to 100 mm, with higher scores indicating worse pain. Both total and subcategory scores are calculated

Time frame
up to one day

Secondary outcomes

1

integrity of the plantar fascia ligament

The Windlass Test is a physical examination technique will be used to assess the integrity of the plantar fascia ligament in the foot. we evaluated the Windlass test, and found it had a high specificity, and a low level of sensitivity. It can be used as part of the clinician's armamentarium in evaluating patients with plantar fasciitis, and should be performed in a weightbearing position to maximize the sensitivity

Time frame
up to one day

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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