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Effect of preoperative eccentric resistance training on perioperative sarcopenia-related motor function in elderly abdominal surgery patients

Effect of preoperative eccentric resistance training on perioperative sarcopenia-related motor function in elderly abdominal surgery patients

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076553
Enrollment
Unknown
Registered
2023-10-11
Start date
2023-10-16
Completion date
Unknown
Last updated
2023-10-16

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

Conditions

Sarcopenia

Interventions

Experimental group:Experimental group:Undergo 3 days of centrifugal resistance training and routine perioperative management 3 days before surgery, and 3 days before surgery to discharge (5th postoper
Control group:Control group:Routine perioperative management 3 days before surgery until (Day 5 after surgery).

Sponsors

Shanghai Fourth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 100 Years

Inclusion criteria

Inclusion criteria: (1) Age 65 and above, gender is not limited; (2) Patients who need elective abdominal surgery; (3) meet the preliminary screening criteria in the Asian Sarcopenia Screening Criteria developed by AWGS in 2019(Possible Sarcopenia,PS); (4) Have the ability to complete relevant assessments and treatments with autonomous activities; (5) Patients and their families who agree to enroll in the group and sign the clinical informed consent form to participate in the study;

Exclusion criteria

Exclusion criteria: (1) Those with severe cognitive and emotional impairments who are unable to cooperate with rehabilitation assessment and treatment; (2) Those who have severe pain before surgery and cannot cooperate with rehabilitation assessment and treatment; (3) The preoperative left ventricular ejection fraction is less than 50%; morbid sinus syndrome, severe sinus bradycardia (< 50 beats/min), or second-degree or greater atrioventricular block without pacemaker; (4) Severe atrophy of major muscle groups caused by motor neurons, peripheral nerves, neuromuscular junctions, muscle lesions and other diseases before surgery, such as spinal rigidity, frostbite, etc.; (5) Patients who have participated in other related clinical studies within 3 months; (6) The patient has a history of previous abdominal surgery; (7) The same patient can only be included once, regardless of whether the cause of the second surgery is related to the first cause.

Design outcomes

Primary

MeasureTime frame
Short Physical Performance Battery;

Secondary

MeasureTime frame
Resting heart rate and blood pressure;Strength, Assistance, Walking, Rise from a chair, Climb stairs ,Falls and Calf surround degree,SARC-CalF;36–item short form health survey , SF-36;Postoperative landing time;Postoperative hospitalization time;Postoperative complication rate;

Countries

China

Contacts

Public ContactGuilong Ma

Shanghai Fourth People's Hospital

maguilong830@126.com+86 158 0175 8778

Outcome results

None listed

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