Skip to content

Effectiveness and safety of a remote multidimensional intervention program in patients with type 2 diabetes mellitus combined with sarcopenia or possible sarcopenia: a randomized, single-blind, controlled study

Effectiveness and safety of a remote multidimensional intervention program in patients with type 2 diabetes mellitus combined with sarcopenia or possible sarcopenia: a randomized, single-blind, controlled study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092510
Enrollment
Unknown
Registered
2024-11-18
Start date
2024-11-18
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Type 2 diabetes mellitus in combination with sarcopenia or possible sarcopenia

Interventions

Control group:Maintain existing medical management without specific remote multidimensional interventions.
intervention group:Receive a 12-week remote multidimensional comprehensive intervention program that included medical guidance, exercise intervention, nutritional intervention, health education, self-

Sponsors

Department of Endocrinology, Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. patients who have completed the registration of initial diagnosis and regular follow-up in the diabetes co-care management cohort of Peking University First Hospital; 2. patients with type 2 diabetes; 3. age > 18 years old; 4. conscious and able to answer questions independently; 5. participate voluntarily in this study; 6. can participate in the intervention trial with the consent of their physician; 7. (Also required for the intervention study) meet any of the following: a. When using a spring-loaded grip strength meter to measure the grip strength of the upper limbs, when the grip strength is <28kg for males and <18kg for females it is considered to be a decrease in muscular strength; b. Physical functioning is assessed using the five-stand-up time, and a five-stand-up time of =12 seconds is considered to be a decrease in physical fitness.

Exclusion criteria

Exclusion criteria: 1. the presence of severe visual or hearing impairments or communication disorders; 2. the presence of cognitive dysfunction or mental retardation; 3. the presence of a terminal illness with a life expectancy of = 6 months; 4. the presence of serious concomitant diseases such as heart, brain, kidney, etc. that prevent them from cooperating with the intervention; 5. the presence of joint pain, fractures and other contraindications to exercise; 6. concurrent participation in other studies. 7. pre-diabetes, type 1 diabetes, special type of diabetes and other non-type 2 diabetes patients.

Design outcomes

Primary

MeasureTime frame
Handgrip strength;Bioelectrical impedance analysis;5-time chair stand test;10-second heel lifts;

Secondary

MeasureTime frame
Height;Weight;waist circumference;Hip measurement;calf circumference;stand on both legs with closed eyes;stand on one leg with open eyes;Quality of Life Assessment Scale SF-36;

Countries

China

Contacts

Public ContactLi Ang

Peking University First Hospital

Liang850513@hotmail.com+86 136 8133 8795

Outcome results

None listed

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