Skip to content

Effectiveness of Supervised Rehabilitation Based on the WeChat Platform on Hip Pain and Functional Improvement in Patients After Hip Arthroscopy for Femoroacetabular Impingement Syndrome: A Randomized Controlled Study

Effectiveness of Supervised Rehabilitation Based on the WeChat Platform on Hip Pain and Functional Improvement in Patients After Hip Arthroscopy for Femoroacetabular Impingement Syndrome: A Randomized Controlled Study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600122650
Enrollment
Unknown
Registered
2026-04-16
Start date
2026-04-16
Completion date
Unknown
Last updated
2026-04-20

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

Conditions

Hip Impingement Syndrome After Hip Arthroscopy

Interventions

Routine Guidance Group:This group of patients received routine rehabilitation guidance for a period of three months. At discharge, patients received routine oral and written discharge instructions and
WeChat Supervision Team:This group of patients received a 3-month supervised rehabilitation intervention based on the WeChat platform. Patients were also given the same printed version of the "FAI P

Sponsors

The Fourth Medical Center of the PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-50 years old; 2. Clinically diagnosed with FAI based on symptoms, signs, and imaging, and has completed arthroscopic surgery; 3. Able to use a smartphone or tablet normally; 4. Good cognitive function, able to cooperate with all rehabilitation treatments; 5. The participant (or their legal representative) has signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Combined with other acute lower limb injuries, fractures, or neurological diseases; 2. Suffering from systemic inflammatory diseases such as rheumatoid arthritis; 3. History of surgery on the same side of the hip; 4. Combined with severe hip osteoarthritis (Tönnis grade >=2); 5. Currently participating in other clinical trials that may interfere with the results of this study.

Design outcomes

Primary

MeasureTime frame
Hip function (iHOT-33 score);

Secondary

MeasureTime frame
Muscle strength (peak torque of major hip musculature);Joint range of motion (active and passive range of motion);Pain (at rest and during daily activities);Balance function;Plantar pressure (static plantar pressure parameters);Hip-related quality of life (HOS-ADL and HOS-SSS scores);Anxiety level;

Countries

China

Contacts

Public ContactLi Xiao

The Fourth Medical Center of the PLA General Hospital

352050114@qq.com+86 130 1120 0409

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 23, 2026