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RecruitingNCT07330635Updated Jan 9, 2026

Chronic Wounds and Blood Circulation Detection

An interventional study of Intervention 1: Mixed exercise program and Intervention 2: High-intensity rowing exercise in Aging, Walking, Difficulty and Chronic Limb-Threatening Ischemia, sponsored by National Health Research Institutes, Taiwan. Recruiting at 1 site in Taiwan. Open to participants aged 20 Years to 95 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-01-09.

Sponsored by National Health Research Institutes, Taiwan · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year 3 months after the study started (first participant enrolled Sep 2024, registered Dec 2025).
  • Started Sep 2024; still recruiting 2 years 1 month later.
Phase
Not applicable
Study type
Interventional
Enrollment
425
Allocation
Randomized
Ages
20 Years to 95 Years
Sex
All
01

Study summary

Lower limb circulatory insufficiency and the associated chronic wounds are common health problems among the elderly. These issues not only affect the individual's mobility and quality of life but also potentially increase medical costs and caregiving expenses. Traditional treatment methods often employ medications to enhance blood circulation, but these clinical approaches have limited effectiveness and induce the risk of side effects. Utilizing exercise as an intervention strategy can help improve lower limb blood circulation in the elderly while reducing the side effects associated with medications. However, due to physical frailty, elderly individuals often cannot participate in high-intensity exercises to improve their circulatory performance.

Therefore, this study will develop a lower limb circulation enhancement exercise system to improve the circulatory performance in individuals with poor lower limb circulation. It will compare the effects of lower limb circulation enhancement exercise, vibration exercise, and mixed exercise on improving blood circulation and functional performance in the elderly or individuals with poor lower limb circulation.

Participants will be randomly assigned into three groups: the lower limb circulation enhancement exercise group, the vibration exercise group, and the mixed exercise group. In addition, a separate group of young adults (control group) will serve as a reference for baseline comparisons. Initially, all participants will undergo a one-time exercise test, followed by a 12-week intervention. The lower limb circulation enhancement exercise group will perform a 30-minute leg press rowing exercise three times a week, while the vibration exercise group will engage in vibration exercise at the same frequency, and the mixed exercise group will perform group-based mixed exercise training at the same frequency. The young adult control group will not receive any intervention but will undergo the same assessments.

Outcome evaluations before and after the intervention include lower limb blood perfusion monitoring, pain scales, and functional performance assessments.

02

Conditions studied

  • Aging
  • Walking, Difficulty
  • Chronic Limb-Threatening Ischemia
  • Chronic Disease

Keywords

  • Poor Lower Limb Circulation
  • Older Adults
  • Chronic Disease
03

In context

Mobility Limitation

317 studies on the registry are indexed under Mobility Limitation; 97 are open to participants now.

This study's planned enrollment of 425 is above the median of 46 across 265 interventional studies indexed under Mobility Limitation.

Browse Mobility Limitation studies →

Lead sponsor

National Health Research Institutes, Taiwan is the lead sponsor of 125 studies on the registry; 29 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 95 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

General criteria (applied to all participants):

Willingness to participate in this study and comply with all study procedures. Able to perform basic physical activity and complete lower limb circulatory and functional assessments.

Normal cognitive function sufficient to understand instructions and provide informed consent.

Group-specific criteria:

Young Adults (Control Group):Aged 20-40 years.No known chronic diseases or peripheral circulatory disorders.Considered healthy volunteers.

Older Adults (Healthy Elderly Group):Aged 65-95 years.No major chronic diseases affecting lower limb circulation.

Older Adults with Chronic Disease (Impaired Circulation Group):Aged 65-95 years.Diagnosed with one or more conditions known to impair peripheral circulation, including but not limited to peripheral arterial disease (e.g., atherosclerosis, thromboangiitis obliterans), chronic venous insufficiency (e.g., varicose veins), diabetes mellitus, hypertension, or hyperlipidemia.

Exclusion criteria

Exclusion Criteria:

Recent acute lower limb injury resulting in tissue exudation, swelling, or other conditions that prevent safe participation in the assessment or intervention procedures.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
425 participants (estimated)

Study arms

  • No intervention
    Young Adults (Reference Control)

    Healthy young adults aged 20-35 years serving as the reference control group. Participants will not receive any intervention but will undergo the same baseline and follow-up assessments of lower limb circulation and functional performance.

  • Experimental
    Older adults (Exercise intervention)

    Older adults aged 65 years. Participants will engage in a 12-week, group-based exercise program (3 sessions per week, 30 minutes per session) focusing on lower limb strengthening, balance, and aerobic training.

    Behavioral: Intervention 1: Mixed exercise program · Behavioral: Intervention 2: High-intensity rowing exercise · Behavioral: Intervention 3: Vibration exercise

  • Experimental
    Older adults with chronic disease (Exercise intervention)

    Older adults aged 65 years and above with chronic disease. Participants will engage in a 12-week exercise program (3 sessions per week, 30 minutes per session).

    Behavioral: Intervention 1: Mixed exercise program · Behavioral: Intervention 2: High-intensity rowing exercise · Behavioral: Intervention 3: Vibration exercise

Interventions

  • BehavioralIntervention 1: Mixed exercise program

    A 12-week, group-based mixed exercise program focusing on lower limb strengthening, balance, and aerobic training (3 sessions per week, 30 minutes per session). Exercise intensity will be adjusted based on individual fitness and circulation levels.

    Also known as: Mixed exercise program

  • BehavioralIntervention 2: High-intensity rowing exercise

    A 12-week, high-intensity lower limb rowing exercise program (3 sessions per week, 30 minutes per session), with individualized intensity adjustments based on each participant's baseline

    Also known as: Lower limb rowing exercise program

  • BehavioralIntervention 3: Vibration exercise

    A 12-week, vibration exercise program (3 sessions per week, 30 minutes per session), with individualized intensity adjustments based on each participant's baseline

    Also known as: Vibration exercise program

06

What researchers measure

Primary outcomes

  1. Lower limb blood perfusion

    Lower limb blood perfusion will be assessed using Laser Doppler Flowmetry (LDF) and Laser Speckle Contrast Imaging (LSCI). For LSCI, measurements will be performed at the plantar surface beneath the hallux. The protocol includes a baseline recording period, transient arterial occlusion using an ankle cuff, and post-occlusion monitoring to capture recovery and reactive changes. Skin perfusion pressure (SPP) will be derived from the LSCI signal inflection point following cuff release, expressed in millimeters of mercury (mmHg).

    Time frame: Baseline and after 12 weeks of intervention

Secondary outcomes

  1. Functional performance (Six-Minute Walk Test)

    Walking distance covered in six minutes on a flat surface, used to assess cardiovascular endurance and functional walking capacity.

    Time frame: Baseline and after 12 weeks of intervention

  2. Functional performance (30-Second Sit-to-Stand Test)

    Number of full sit-to-stand repetitions completed in 30 seconds from a standard chair without using the arms, used to evaluate lower limb strength and functional mobility.

    Time frame: Baseline and after 12 weeks of intervention

  3. Functional performance (10-Meter Walk Test)

    Walking speed over a 10-meter distance at a comfortable pace, measured to assess gait performance and walking efficiency.

    Time frame: Baseline and after 12 weeks of intervention

07

Study locations

1 of 1 sites recruiting
  • National Center for Geriatrics and Welfare Research, National Health Research Institutes
    Taipei, Taiwan
    Recruiting
08

References and documents

Individual participant data

Plan to share: No — No plan to share individual participant data (IPD) due to participant privacy protection and institutional policy restrictions.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07330635
Lead sponsor
National Health Research Institutes, Taiwan
Responsible party
Sponsor
First posted
Jan 9, 2026
Start date
Sep 4, 2024
Primary completion
Sep 4, 2027 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Jan 9, 2026

Study contacts

Po-Jung Chen, Ph.D.
Contact
pojungchen@nhri.edu.tw
+886-5-632-5080 ext. 17
Chueh-Ho Lin, Ph.D.
Contact
chueh.ho@nhri.edu.tw
+886-5-632-5080 ext. 15

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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