The effectiveness of Tele-resistance exercise programing in patients with sarcopenia after hip fracture surgery

Phase 3

Recruiting

• Conditions: Patients with sarcopenia after hip fracture surgery; Hip fracture, Sarcopenia, Tele-resistance exercise

• Registration Number: TCTR20220123001
• Lead Sponsor: Siriraj Medical Research Center

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2022-01-23
• Study Completion: 2022-12-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 54

Inclusion Criteria

1.Patients aged from 60 to 90 years old who were diagnosed with femoral neck fracture and underwent bipolar hemiarthroplasty at Siriraj hospital since January 2022
2. Patients who were diagnosed with sarcopenia based on Asian Working Group for Sarcopenia 2019 : hand grip strength < 28 kg and appendicular skeletal muscle mass < 7 kg/m2 in in men by BIA, hand grip strength < 18 kg and appendicular skeletal muscle mass < 5.7 kg/m2 in in women by BIA
3. Patients who can communicate in Thai
4. TMSE >= 20
5. Patients who were allowed to ambulate with weight bearing as tolerated post-surgery
6. Patients had the ability to walk independently or walk with a gait aid for at least 5 meters prior to having fracture
7. Patients had a caregiver who took care when patients did exercise
8. Patients had a mobile phone, computer or electronic device that could access internet
9. Patients who had no limitation of vision or hearing that affect exercise via video and real time video-conference

Exclusion Criteria

1. Patients denied to participate in the research
2. Femoral neck fracture from pathologic fracture
3. Patients with post-operative complications that adversely affect the ability to exercise
4. Patients had a disease that affects exercise, such as severe cardiovascular disease, severe respirator disease, dementia, musculoskeletal problem, hemiparesis that could not against gravity or psychiatric disease
5. Patients had a cardiac pacemaker

Study & Design

• Study Type: Interventional
• Study Design: Not specified