Skip to content

Evaluation of exercise on individuals with dementia and their carers

A randomised controlled evaluation of exercise as a therapy for the behavioural and psychological symptoms of dementia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN01423159
Enrollment
145
Registered
2009-05-26
Start date
2009-08-01
Completion date
Unknown
Last updated
2018-09-10

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

Conditions

Behavioural and psychological symptoms of dementia Mental and Behavioural Disorders Unspecified dementia

Interventions

A 6-week supervised incremental course of walking outside, at a pace and distance to suit the participant and carer for at least 5 days per week. Walking is a useful exercise which is considered accep

Sponsors

Central and North West London NHS Foundation Trust (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Both males and females, no age limits 2. Diagnosis of: 2.1. Dementia in primary or secondary care OR 2.2. Suspected dementia confirmed by the researcher to ensure the International Classification of Diseases 10th Revision (ICD-10) research criteria for dementia (DCR-10) are met 3. Presence of a carer (professional, friend or family member, who does not necessarily have to live with the participant) 4. Neuropsychiatric Inventory (NPI) score in any one sub-set except only hallucination or delusion more than or equal to 2 in severity and more than or equal to 2 in frequency 5. Consent of participant, or in the case of an individual who is not capable of giving informed consent, the assent of the participant with agreement of carer 6. Consent of carer

Exclusion criteria

Exclusion criteria: 1. Cardio-respiratory condition, neurological or musculo-skeletal condition of a degree that prevents participation to even the modified exercise regime unsafe or not possible 2. A score of three or more assessed using the Falls Risk Assessment Tool or less than one minute as assessed by the Timed Unsupported Steady Stand test 3. Uncontrolled medical problems, which the GP considers would exclude participants from undertaking the exercise programme; for example, acute systemic illness such as pneumonia, poorly controlled angina, acute rheumatoid arthritis, unstable or acute heart failure 4. Sensory impairment to an extent that prevents dyad facilitated exercise 5. Participant or carer dissent to engage in the exercise programme 6. Acute confusional state

Design outcomes

Primary

MeasureTime frame
Behavioural and psychological symptoms measured by NPI at baseline, week 6 and 12.

Secondary

MeasureTime frame
1. Participants' mental health (General Health Questionnaire) at baseline, week 6 and 12 2. Participants' quality of life (DemQOL-Proxy) at baseline, week 6 and 12 3. Caregivers' burden of caring (short Zarit Caregiver Burden Inventory) at baseline, week 6 and 12 4. Participants' level of physical activity and compliance with the intervention (diaries and heart rate monitors, to be completed by the participant and their carer) 5. Participants' and carers' views about the intervention (Diaries and semi-structured questionnaires to be carried out after the trial) 6. Mortality and domiciliary status at 6 months

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 31, 2026