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Gait Training in Dementia

Evaluating of Gait Characteristic following The Rehabilitation of Gait in Dementia (ReGait-DEM)

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626001016325
Acronym
ReGait-DEM
Enrollment
24
Registered
2026-08-18
Start date
2026-04-27
Completion date
2026-05-22
Last updated
2026-08-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

The purpose of the study is to assess the feasibility and preliminary effects of implementing the ReGait-DEM Training Program among older adults with moderate dementia, including the Gait changes, Quality of life, Neuropsychiatric symptoms and Functional Indenpendency.

Interventions

A pilot study will be conducted involving 24 older adults with moderate dementia recruited from Hospital Canselor Tuanku Muhriz (HCTM), Universiti Kebangsaan Malaysia. Participants will be approached face-to-face at the Occupational Therapy Unit of HCTM. The Rehabilitation on Gait in Dementia (ReGait-DEM) Training Program will be implemented monitoring by certified physiotherapist and occupational therapist. This structured 12-week intervention is designed to improve gait, balance, and cognitive

A pilot study will be conducted involving 24 older adults with moderate dementia recruited from Hospital Canselor Tuanku Muhriz (HCTM), Universiti Kebangsaan Malaysia. Participants will be approached face-to-face at the Occupational Therapy Unit of HCTM. The Rehabilitation on Gait in Dementia (ReGait-DEM) Training Program will be implemented monitoring by certified physiotherapist and occupational therapist. This structured 12-week intervention is designed to improve gait, balance, and cognitive function among older adults with moderate dementia. The program integrates motor and cognitive components through progressive dual-task and multitasking exercises targeting executive function and attentional processes (Keeffe et al., 2020). Upon confirmation of eligibility, caregivers will receive a one-to-one briefing, including a one-hour demonstration of the program within one week prior to commencement. The intervention consists of 3 level home-based rehabilitation sessions delivered twice weekly (total of 24 session in 12-week intervention). The duration and progression of the intervention may be adjusted according to the clinical needs of each participant. Participants will be provided with a training manual and a session Daily Training Log to support adherence. Monthly follow-up sessions will be conducted either face-to-face at the hospital or through home visits to review progress, address challenges, and modify the program as needed. The training protocol includes stretching, dual-task activities, gait and balance exercises and cognitive tasks, with an intended duration of at least 30 minutes per session at mild-to-moderate intensity. Outcome assessments will be conducted at baseline (0 exercise session), Week 6 (after 12 sessions of exercise), and Week 12 (after 24 sessions of exercise). The ReGait-DEM Training Program will be administered as a caregiver-assisted home-based rehabilitation program. Caregivers will be trained by a certified physiotherapist and occupational therapist prior to the intervention and will guide the participants during each session at home using the provided training manual and Daily Training Log. The exercises will include progressive motor-cognitive and dual-task activities such as walking while counting, walking while repeating words, taking and placing a cup while turning, identifying colours while stepping, simple balance activities, gait practice, stretching, and functional movement tasks. These exercises will be performed according to the participant’s ability and progressed across three levels throughout the 12-week intervention.

Sponsors

Universiti Kebangsaan Malaysia (UKM)
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Each Program will be composed of one Caregiver and one participant with moderate dementia. The participant moderate dementia must: - Older adults aged greater than or equal to 60 years - Moderate Dementia (Clinical Dementia Rating (CDR) Scale: 2, Montreal Cognitive Assessment (MoCA): 10-17) - Participants must be ambulatory, either independently without assistive devices or with the use of walking aids (e.g., cane or walker), and capable of following simple one- to two-step commands - Medically stable; with no acute illness that limits mobility. - Have a primary caregiver willing and able to participate in training sessions. - Low to moderate risk of fall person (Able to sustain more than 10 second in Single-Leg Stance Test) - No significant eyes problem - Provide informed consent The Caregiver in this program must: 1)Live with the participant with dementia and/or providing some portion of their daily care including Activities of Daily Living in an informal capacity. 2) Be able to speak and understand English/Bahasa Malaysia 3) Residence within 30 km of the hospital sites. 4) Adequate vision, hearing, cognition and manual dexterity sufficient to understand the training given.

Exclusion criteria

1) Older adults with mild and severe dementia 2) Cognitively healthy older adults without dementia. 3) Have an unstable cardiovascular condition, rheumatic disease that caused limitation of range of motion or pain. 4) Presence of musculoskeletal, orthopaedic and neurological impairments that would affect their gait 5) History of stroke and psychiatric disorders. 6) High Risk of falls 7) Unable to understand instructions.

Outcome results

None listed

Source: ANZCTR · Data processed: Aug 31, 2026