Effects of Marching Exercise With Cognitive Training on Physical, Cognitive Function, and Autonomic Cardiovascular Responses in Older Adults With Type 2 Diabetes Mellitus

NCT07330700 | Completed DMC

• 1 other identifier: UPhayaoChonticha-221
• Study Type: interventional
• Target: 60
• Locations: 1 country
• Sites: 1

Brief Summary

This study aims to evaluate the effects of a combined marching exercise with cognitive training program on physical performance, cognitive function, and autonomic cardiovascular responses in older adults with type 2 diabetes mellitus. Participants will be randomly assigned to either an intervention group receiving marching exercise with cognitive tasks or a control group receiving usual care. Outcomes will be assessed before and after the intervention period. The findings are expected to provide evidence for a feasible and safe exercise strategy to improve physical and cardiovascular health in older adults with type 2 diabetes.

Conditions

Type2 Diabetes Mellitus; Autonomic Nervous System Imbalance

Keywords

Type2 Diabetes Mellitus; Dual-task Exercise; Marching Exercise; Autonomic Nervous System; Heart Rate Variability

Outcome Measures

Primary Outcomes (9)

• Heart rate variability (HRV)

  Heart Rate Variability (HRV) Assessment HRV is assessed using the SA-3000P device to evaluate Autonomic Nervous System (ANS) function, stress resistance, and arterial elasticity. The procedure involves a 3-minute measurement using a finger probe while the subject sits quietly. The device automatically analyzes the data to provide time-domain indices (such as SDNN), which are used to assess cardiac function and prognosis.

  Baseline, immediately after 6 weeks of intervention, and 1-month follow-up

• Handgrip strength test

  Handgrip Strength Testing This test assesses hand and forearm muscle strength using a hand grip dynamometer. The subject stands upright with the dominant arm extended alongside the body (abducted approx. 15 degrees), elbow straight, and palm facing down. Upon the "start" signal, the subject squeezes the device as hard as possible.

  Baseline, immediately after 6 weeks of intervention, and 1-month follow-up

• Five times sit-to-stand test (FTSST)

  Leg Muscle Strength Test (FTSST) The Five Times Sit to Stand Test measures leg strength using a standard armless chair. The subject performs five consecutive stand-to-sit cycles as quickly and safely as possible from a seated position (hips \~90°). Time is recorded from the start signal until the final return to sitting. The average of three trials is calculated (Kaewjoho et al. 2020).

  Baseline, immediately after 6 weeks of intervention, and 1-month follow-up

• Timed Up and Go Test (TUGT)

  Assessing Balance Ability (TUGT) The Timed Up and Go Test (TUGT) evaluates dynamic balance and fall risk. The subject starts seated, stands up on signal, walks 3 meters around a cone, and returns to sit as quickly and safely as possible. The average time of three trials is recorded.

  Baseline, immediately after 6 weeks of intervention, and 1-month follow-up

• Static Balance Single-leg stance test (SLST)

  Static Balance (SLST) The Single-leg stance test assesses static balance. The subject stands on their dominant leg with the other knee bent at 90° and arms crossed over the chest. Timing measures how long the position is maintained without error (e.g., foot touching the ground, moving arms). The average time of three trials is calculated in seconds.

  Baseline, immediately after 6 weeks of intervention, and 1-month follow-up

• 6-minute walk test

  6-Minute Walk Test (6MWT) This test assesses cardiopulmonary endurance. The subject walks as fast as possible (without running) for 6 minutes on a rectangular course (45m perimeter). Resting is allowed, but the timer continues. The total distance covered is measured to calculate VO2max.

  Baseline, immediately after 6 weeks of intervention, and 1-month follow-up

• Motor-Cognitive Dual-Task Test:

  Motor-Cognitive Dual-Task Test (S-TMT) The Stepping Trail Making Test assesses dual-task motor-cognitive function. The subject steps on squares numbered 1 to 16 in order as quickly and accurately as possible. The time taken to complete the sequence, including any error corrections, is recorded. The test is performed only once.

  Baseline, immediately after 6 weeks of intervention, and 1-month follow-up

• Motor-Cognitive Dual-Task Test

  Motor-Cognitive Dual-Task Test (F8WT) The Figure-of-8 Walk Test assesses dynamic balance and turning ability. The subject walks a figure-of-8 pattern around two cones spaced 1.5 meters apart. Time is recorded for one complete lap. In the Dual-Task variation (F8WT-MC), the subject performs the walk while holding a cup of water in their dominant hand.

  Baseline, immediately after 6 weeks of intervention, and 1-month follow-up

• Montreal Cognitive Assessment (MoCA)

  Assessment of Cognitive Impairment (MoCA) The MoCA test is a screening tool for cognitive impairment covering various brain functions (e.g., memory, attention). It involves a 10-15 minute interview with a maximum score of 30. A score below 26 indicates mild cognitive impairment (MCI).

  Baseline, immediately after 6 weeks of intervention, and 1-month follow-up

Study Arms (3)

Modified Marching Exercise combined with Cognitive Training

EXPERIMENTAL

Participants in this group perform a Modified Marching Exercise combined with dual-task cognitive training. The exercise consists of rhythmic marching movements while simultaneously performing cognitive tasks such as backward counting and reciting months in reverse order. Each session lasts approximately 30 minutes and is conducted according to the assigned intervention protocol.

Other: Modified Marching Exercise combined with cognitive training group

Modified Marching Exercise

EXPERIMENTAL

Participants in this group perform the Modified Marching Exercise alone without concurrent cognitive tasks. The exercise involves rhythmic marching movements adapted to individual functional ability. Each session lasts approximately 30 minutes and follows the same frequency and duration as the experimental intervention.

Other: Modified Marching Exercise group

Control group

NO INTERVENTION

Participants in the control group receive health education and educational pamphlets focused on fall prevention. They continue their usual daily activities without participation in a structured exercise program during the study period.

Interventions

Modified Marching Exercise combined with cognitive training group OTHER

The exercise program consists of a Modified Marching Exercise that emphasizes lifting the knees to touch a designated rope during each step. A metronome is used to maintain a rhythmic pace of 60-80 beats per minute throughout the training. In addition, participants perform concurrent cognitive dual-task training designed to stimulate executive function. The cognitive tasks include countdown calculations, backward sequencing of months and weekdays, and a Stroop interference task. Each session lasts approximately 30-40 minutes and includes a 5-minute warm-up and a 5-minute cool-down. Exercise intensity is individually adjusted according to the participant's fitness level. The program is conducted three times per week for 6 consecutive weeks, for a total of 18 sessions. This combined cognitive-motor training is designed to integrate physical and cognitive demands in order to improve movement efficiency, balance control, and responses to daily functional stimuli.

Also known as: MME with Dual-task Marching Exercise

Modified Marching Exercise combined with Cognitive Training

Modified Marching Exercise group OTHER

Participants perform a structured Modified Marching Exercise program. The exercise involves rhythmic marching movements with pace controlled by a metronome set at 80 beats per minute. The intervention is conducted three sessions per week for 6 weeks, with each session lasting approximately 30-40 minutes, including warm-up and cool-down periods. All exercise sessions are supervised by a licensed physical therapist.

Also known as: MME

Modified Marching Exercise

Eligibility Criteria

• Age: 60 Years - 80 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Male and female.
• Aged between 60 and 79 years.
• Medically diagnosed with type 2 diabetes.
• Peripheral neuropathy with a score of 7 or higher according to the Michigan Neuropathy Screening Instrument (MNSI).
• Body Mass Index (BMI) within the normal range (between 18.5-24.5 kg/m²).
• Able to follow instructions and willing to participate in the study.
• Able to communicate with researchers and provide information independently (researchers will read the questions to the volunteers and allow them to choose their own answers).
• Able to walk continuously for at least 10 meters without the use of walking aids.

You may not qualify if:

• Neurological disease (e.g., stroke, Parkinson's disease, spinal cord injury) that affects mobility, such as balance and gait.
• Open wounds on the skin that affect weight-bearing while standing or walking. 1) Deformities or abnormalities of the extremities, or disabilities resulting from the loss of limbs that may affect the study.
• \) Inflammation of joints and muscles, or musculoskeletal conditions with a pain score greater than 5 out of 10 on the Visual Analogue Scale (VAS), or any pain that affects the study.
• \) A history of ankle, knee, or hip joint replacement within 6 months prior to participation in the study, or any residual effects from surgery that affect the study.
• \) Hearing and vision impairments that cannot be corrected with hearing aids and glasses, etc.
• \) Other complications that may affect the study, such as dizziness, angina pain, uncontrolled high blood pressure, acute illness, or injury, etc.

Sponsors & Collaborators

• Chonticha Kaewjoho: lead
• University of Phayao: collaborator

Study Sites (1)

Chonticha Kaewjoho

Phayao, 56000, Thailand

Location

MeSH Terms

Interventions

MME

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: SINGLE
• Who Masked: PARTICIPANT
• Masking Details: Participants are blinded to group allocation. Due to the nature of the exercise interventions, care providers and investigators are not blinded.
• Purpose: TREATMENT
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR INVESTIGATOR
• PI Title: Chonticha Kaewjoho

Model Details: Participants are randomly assigned to one of three parallel groups: 1. Modified Marching Exercise combined with cognitive training 2. Modified Marching Exercise alone, or 3. Control group receiving usual care. Outcomes are assessed before and after the 6-week intervention period.

Study Record Dates

• First Submitted: December 28, 2025
• First Posted: January 9, 2026
• Study Start: July 10, 2025
• Primary Completion: November 5, 2025
• Study Completion: December 10, 2025
• Last Updated: January 14, 2026

Record last verified: 2026-01

Locations

TH (1)