Integrated Exercise Therapy Interventions on the Performance and Injury Prevention in Competitive… (NCT04384003) | Clinical Trial Compass
UnknownNot Applicable
Integrated Exercise Therapy Interventions on the Performance and Injury Prevention in Competitive Sports
Taiwan60 participantsStarted 2019-08-01
Plain-language summary
Football is an increasingly popular exercise and common practice among adolescent and elite athletes. However, these athletes tend to have injuries involving the lower extremity and foot. Recent literature has proposed a promising concept of core stability on the arch of the foot and proximal hip control exercise for a knee injury. They have highlighted that foot core training begins with targeting the plantar intrinsic muscles through exercise intervention, which may enhance the capacity and control of the foot core system. Moreover, it is hypothesized that the 'complexity algorithm' of exercise intervention for proximal hip control may provide more sufficient effects on musculoskeletal pain in the lower extremity. However, some conflicting issues such as assessment and training of foot intrinsic muscle in functional positions still largely lack devices and research to elucidate the underlying mechanism of its development and integrated exercise interventions proximally and distally on these athletes.
Firstly, the investigators aim to design and develop of novel intrinsic foot muscle assessment and training device for sporting tasks and to examine the feasibility and reliability of muscle stiffness in foot and hip joints before and after exercise intervention using shear wave ultrasound elastography (SWUE) in athletes without and with foot and ankle overuse injuries; second, investigators will investigate whether immediate and persistent alteration after the integrated therapeutic exercise on motor control and muscle stiffness.
Who can participate
Age range
15 Years – 40 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion criteria
. Diagnosis of painful heel syndrome by clinical examination, with the following positive clinical signs:
. Pain in the morning or after sitting a long time
. Local pain where the fascia attaches to the heel
. Increasing pain with extended walking or standing for more than 15 minutes
. Was associated with inflammatory symptoms (pain, swelling, etc.)
. Pain in the area of the insertion of the plantar aponeurosis on the medial tubercle of the calcaneus.
. Not perform ankle stretching exercises as treatment of the plantar fasciitis.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Cross-sectional area (CSA)
Timeframe: 6 months
2
Cross-sectional area (CSA)
Timeframe: 12 months
3
Thickness
Timeframe: 6 months
4
Thickness
Timeframe: 12 months
5
Stiffness (RTE)
Timeframe: 6 months
6
Stiffness (RTE)
Timeframe: 12 months
7
Joint kinematics and joint kinetics in the hip, knee and ankle joints will be calculated with the data
Timeframe: 12 months
8
Joint kinematics and joint kinetics in the hip, knee and ankle joints will be calculated with the data
. A neutral foot alignment: determined by measurement of the resting calcaneal stance position (RCSP: between 2°of inversion and 2°of eversion) and scores on the navicular drop (ND: between 5 and 9 mm) test.
Exclusion criteria
. Traumatic injury to lower limbs which impacted joint integrity and function (i.e., fractures) resulting in at least 1 interrupted day of desired physical activity
. History of spinal, pelvic or lower limb surgery
. Major neurological, cardiorespiratory or circulatory disorders
. Past history of traumatic head injury with or without loss of consciousness
. Have been taking non-steroidal anti-inflammatory or corticosteroid medication in the past month
. Recent intervention/management within the last 6 months