Skip to content

Research on comprehensive rehabilitation treatments and telemedicine platform for foot and ankle injuries in military training

Research on comprehensive rehabilitation treatments and telemedicine platform for foot and ankle injuries in military training

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084264
Enrollment
Unknown
Registered
2024-05-13
Start date
2022-07-01
Completion date
Unknown
Last updated
2024-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic plantar heel injure in military training

Interventions

Shockwave combined ultrasound drug introduction Group:Shockwave combined ultrasound drug introduction, routine rehabilitation
Shockwave Group:Shockwave, routine rehabilitation

Sponsors

Chinese PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1)20-80 years old; 2) foot and ankle injury diagnosed by pathology or imaging; 3) duration of foot and ankle pain =1 month and VAS Score =3 points; 4) absence of an unhealed wound in the foot; and 5) failed with general physical therapy.

Exclusion criteria

Exclusion criteria: 1) age:=20 years or =80 years; 2) with severe cardio-pulmonary disease, lower extremity infection or vascular disease; 3) diabetes mellitus, osteoporosis, lactation, pregnancy, neurological dysfunction, coagulopathy; 4) with unhealing foot wound; 5) significant anxiety and depression; 6) with eczema or other skin diseases.

Design outcomes

Primary

MeasureTime frame
visual analogue scale (VAS);Cumberland scale;Foot and Ankle Ability Measure (FAAM);American Orthopaedic Foot and Ankle Society (AOFAS);

Secondary

MeasureTime frame
Y-balance test;Star Excursion Balance Test (SEBT);Functional Near-Infrared Spectroscopy (fNIRS);

Countries

China

Contacts

Public ContactHuimin Xie

Chinese PLA General Hospital

emily030218@126.com+86 130 2191 9118

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026