Implementation of a Minimal Equipment Exercise Intervention in Community-dwelling Older Adults With Dementia

ConditionDementia
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age55+
SponsorGeriatric Education and Research Institute

About this trial

The aim for this study is to investigate the effectiveness of a 16-week minimal-equipment progressive resistance training program compared to usual care, in improving functional outcomes among older adults with dementia in Singapore.

Participants will:

* receive either minimal-equipment progressive resistance training or continue with usual care * perform physical and cognitive function tests at three time-points

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged 55 years or older

Community-dwelling

Formal medical diagnosis of dementia of any cause

Disqualifiers

Diagnosis of neurological and/or myopathic disorders

Severe audio-visual impairment

Severe mobility impairment that affects study participation

Not suitable to participate in exercise intervention as deemed by a nursing staff or allied health professional

Trial design

Design model

Parallel

Treatments tested in this trial

  • Minimal-equipment progressive resistance training

    Other intervention

    The intervention consists of resistance training exercises that target major upper and lower body muscle groups with the use of portable equipment such as resistance bands and wrist/ankle weights. The exercise dosage will be progressively increased across the 16 weeks to achieve training adaptations. The exercise programme will be conducted three times per week, with each session lasting approximately 30 to 45 minutes.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Progressive resistance trainingExperimental treatment 1 intervention
Group B: Usual CareNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Change in handgrip strength

This test is a measurement of upper limb strength. Handgrip strength will be measured in kilograms using a Jamar Plus + Digital Hand Dynamometer. Participants will squeeze the dynamometer with maximum effort in a seated position with their arms at their sides and elbows flexed at 90 degrees. Two trials will be administered for each arm and the highest of four readings will be used for analysis.

Time frame
Baseline, Mid-intervention (Week 9), Post-intervention (Week 17)
2

Change in five times sit-to-stand test

This test is a measurement of lower limb strength. Participants will be instructed to perform five chair stands as fast as possible using a chair without arms, and the time recorded will be used for analysis.

Time frame
Baseline, Mid-intervention (Week 9), Post-intervention (Week 17)
3

Change in 30-seconds sit-to-stand test

This test is a measurement of lower limb strength and power. Participants will be instructed to perform repeated chair stands as fast as possible using a chair without arms, and number of completed full stands will be recorded for analysis.

Time frame
Baseline, Mid-intervention (Week 9), Post-intervention (Week 17)

Secondary outcomes

1

Change in Time Up and Go test

This test is a measurement of functional mobility. The test measures the time taken for participants to rise from a seated position, walk three metres at a comfortable speed, make a turn, walk back, and return to a seated position. Two trials will be administered, and the mean reading will be used for analysis.

Time frame
Baseline, Post-intervention (Week 17)
2

Change in Short Physical Performance Battery test

This test is a measurement of physical function that consists of three components inclusive of 4-metre gait speed test, five times sit-to-stand test and a progressive test of standing balance.

Time frame
Baseline, Post-intervention (Week 17)
3

Change in gait speed test

The test measures the time taken for participants to walk six metres at a normal pace from a moving start without deceleration. Two trials will be administered, and the mean reading will be used for analysis.

Time frame
Baseline, Post-intervention (Week 17)
4

Change in functional reach test

This test is a measurement of dynamic balance. While standing with their back to the wall, participants are instructed to reach forward with their dominant arm outstretched at shoulder level while maintaining a fixed stance. The distance between the metacarpal bone of the third finger in the initial position and the maximum point reached is measured. Two trials will be administered, and the better reading will be used for analysis.

Time frame
Baseline, Post-intervention (Week 17)

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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