The Effect of IoT-based Smart Exercises System in the Senior Adults: Resistance Band Training System

ConditionOlder Adults
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50+
SponsorNational Cheng-Kung University Hospital

About this trial

Subjects are divided into two groups, (1) Control (Ctrl) and (2) Smart Exercise (SE) group. Participants in the Ctrl group are instructed to perform resistance band training twice weekly according to a paper-based exercise guide, whereas participants in the SE group are instructed to perform resistance band training twice weekly for 12 weeks using the Resistance Band Training System. The physical fitness tests and questionnaire of both groups are performed before and after the 12-week exercise program.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Adult over 50 years old

No significant limb disability or joint deformation

No history of cardiovascular disease

Never lost balance due to dizziness in the past 12 months

Disqualifiers

limb disability or joint deformation

history of cardiovascular disease

lost balance due to dizziness in the past 12 months

cognitive deficits

Trial design

Design model

Parallel

Treatments tested in this trial

  • Smart Elastic Band App

    Device

    Participants in the SE group perform resistance band training using the Resistance Band Training System twice weekly for 12 weeks, with each session lasting approximately 30 minutes. Training sessions and exercise completion are recorded by the system.

  • Paper-based Resistance Band Exercise Guide

    Behavioral

    Participants in the Ctrl group are instructed to perform resistance band training twice weekly for 12 weeks according to a paper-based exercise guide, with each session lasting approximately 30 minutes.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Control groupActive comparator 1 intervention
Group B: Smart Exercise groupExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Six-minute walk test

To walk as much as possible within six minutes and measure the total distance traveled.

Time frame
baseline
2

Six-minute walk test

To walk as much as possible within six minutes and measure the total distance traveled.

Time frame
after 12-week intervention

Secondary outcomes

1

BMI

Participant's weight in kilograms divided by the square of height in meters is recorded as Body Mass Index (BMI).

Time frame
baseline
2

BMI

Participant's weight in kilograms divided by the square of height in meters is recorded as Body Mass Index (BMI).

Time frame
after 12-week intervention
3

SMI

Skeletal muscle mass index (SMI), which is the sum of the muscle masses of the four limbs as appendicular skeletal mass (ASM) in kilograms divided by the square of height in meters, is detected by bioelectrical impedance analysis.

Time frame
baseline
4

SMI

Skeletal muscle mass index (SMI), which is the sum of the muscle masses of the four limbs as appendicular skeletal mass (ASM) in kilograms divided by the square of height in meters, is detected by bioelectrical impedance analysis.

Time frame
after 12-week intervention

Other outcomes

Sponsors and contacts

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