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Chair-bound Exergaming in Pre-frail/ Frail Older Adults in Nursing Home

H

Hong Kong Metropolitan University

Status

Enrolling

Conditions

Frailty in Older Adults

Treatments

Behavioral: Exergaming

Study type

Interventional

Funder types

Other

Identifiers

NCT06849557
HE-SF2024/58

Details and patient eligibility

About

This pilot randomized controlled trial is designed to investigate the effectiveness of chair-bound exergaming on improving physical and cognitive function in pre-frail/ frail nursing home residents

Full description

Objective To explore the effects of the chair-bound exergaming on the enjoyment of physical activity in in pre-frail/ frail nursing home residents.

To evaluate the effects of the chair-bound exergaming in improving physical and cognitive function in pre-frail/ frail nursing home residents.

Research plan and methodology Thirty nursing home residents will be recruited from the nursing homes.

All the eligible participant will be randomly allocated to either one of the following 2 groups (i) Exergaming (intervention group), or (ii) wait list control.

  1. Intervention group (exergaming group, ERG) Those allocated to the ERG will receive supervised chair-bound exercise programme for 12 weeks.
  2. Control group (wait list control, CG) Those allocated to the CG will receive supervised chair-bound exercise programme for 12 weeks after post-assessment.

Enrollment

30 estimated patients

Sex

All

Ages

60+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • older adults aged 60 years or older living in the nursing homes;
  • pre-frail or frail according to the Fried Frailty Phenotypes;
  • ability to understand and execute instructions; and
  • ability to sit unassisted on a chair or in a wheelchair.

Exclusion criteria

  • no controlled medical diagnosed of severe cardiometabolic, respiratory and musculoskeletal disorders;
  • any conditions that hinder the participation of intervention and assessment; and
  • being involved in any other clinical trials.

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 2 patient groups

Wait-list Control
No Intervention group
Description:
Wait list control, after post-test, 12 week supervised exercise intervention
Exergaming
Experimental group
Description:
12-week exergaming intervention
Treatment:
Behavioral: Exergaming

Trial contacts and locations

1

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Central trial contact

Bonny YM Wong

Data sourced from clinicaltrials.gov

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