Actively Recruiting

Phase Not Applicable
Age: 20Years - 95Years
All Genders
Healthy Volunteers
ID07330635

Constructing a Holistic Care New Model for Chronic Wounds and Blood Circulation Detection to Enhance Home Care Quality

Led by National Health Research Institutes, Taiwan · Updated on 2026-01-09

425

Participants Needed

1

Research Sites

16 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Lower limb circulatory insufficiency and chronic wounds are common issues among elderly individuals, impacting mobility, quality of life, and increasing medical costs. Traditional drug treatments have limited effects and potential side effects. This research aims to develop and compare different exercise methods to improve blood circulation and functional performance in older adults or those with poor lower limb circulation, including a comparison group of healthy young adults as a reference. Participants will be randomly assigned to one of three exercise groups: a lower limb circulation enhancement exercise group performing leg press rowing, a vibration exercise group, and a mixed exercise group combining strengthening, balance, and aerobic training. Each group exercises for 30 minutes, three times a week, over 12 weeks. A separate healthy young adult control group will not receive any intervention but will undergo the same assessments for baseline comparison. Throughout the study, participants will be evaluated before and after the 12-week period using lower limb blood perfusion monitoring, pain scales, and functional performance tests such as the Six-Minute Walk Test, the 30-Second Sit-to-Stand Test, and the 10-Meter Walk Test. These assessments will help measure changes in circulation and physical function. The study will monitor participants' adherence and safety during the intervention period, which contributes to understanding the impact of these exercise programs on blood flow and mobility.

CONDITIONS

Brief Title

Chronic Wounds and Blood Circulation Detection

Who Can Participate

Age: 20Years - 95Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Willingness to participate and comply with all study procedures
  • Ability to perform basic physical activity and complete lower limb circulation and functional assessments
  • Normal cognitive function to understand instructions and provide informed consent
  • For young adults: aged 20-40 years with no known chronic diseases or peripheral circulatory disorders
  • For older adults (healthy group): aged 65-95 years with no major chronic diseases affecting lower limb circulation
  • For older adults with chronic disease: aged 65-95 years diagnosed with conditions impairing peripheral circulation such as peripheral arterial disease, chronic venous insufficiency, diabetes mellitus, hypertension, or hyperlipidemia
Not Eligible

You will not qualify if you...

  • Recent acute lower limb injury causing tissue exudation, swelling, or other conditions preventing safe participation in assessments or exercise interventions

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 12 weeks

Participants engage in a 12-week exercise program focusing on lower limb strengthening, balance, and aerobic training, or a high-intensity rowing or vibration exercise program, depending on their assigned group. Healthy young adults serve as a control group and do not receive an intervention but participate in the same assessments.

3 sessions per week, 30 minutes per session

Follow-up

Duration - Immediately after treatment

Participants undergo assessments of lower limb blood perfusion and functional performance after completing the intervention period.

1 visit (in-person)

Trial Site Locations

Total: 1 location

1

National Center for Geriatrics and Welfare Research, National Health Research Institutes

Taipei, Taiwan

Actively Recruiting

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Research Team

P

Po-Jung Chen, Ph.D.

C

Chueh-Ho Lin, Ph.D.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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