Skip to content

Evaluation of a preventative multi-disciplinary training program for prospective memory among older adults

Evaluation of a preventative multi-disciplinary training program for prospective memory among older adults: a randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN57600070
Enrollment
84
Registered
2017-01-11
Start date
2016-05-01
Completion date
Unknown
Last updated
2021-05-24

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

Conditions

Memory function Mental and Behavioural Disorders Memory function

Interventions

Participants will be randomly assigned to the intervention or control groups (1:1) in site-specific blocks that vary randomly in size to ensure adequate randomization, developed by http://www.randomiz
intention implementation intentions). Control group: Participants receive no additional treatment and continue as normal for the duration of the study. Follow up take

Sponsors

Universiti Putra Malaysia
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 60 years and above 2. Educational level of at least secondary educational level

Exclusion criteria

Exclusion criteria: 1. Aged less than 60 years old 2. Are not educated enough or are illiterate 3. Those who do not show normal cognitive functions 4. Suffering from a psychological or learning disability 5. History of nuerological impairments (measured by MMSE) 6. Any major psychiatric disorders (taking any psychoactive medication (e.g., anti-depressive, anxiolytics)) and learning disabilities 7. History of general anaesthesia, head truamas (in the last 6 months prior to the study), cerbrovascular disease, or neurological impairments 8. Drug/alcohol abuse

Design outcomes

Primary

MeasureTime frame
Prospective memory (PM) functions are assessed at baseline, 6, 10 and 14 weeks using: 1. PM functions (time-, event-, and activity-based PM) are assessed using a computer-based test 2. PRMQ (a paper-pencil questionnaire) to be used as a subjective measure for PM functions

Secondary

MeasureTime frame
1. Instrumental daily living activities are measured using the Instrumental Activities of Daily Living Scale at baseline, 6, 10 and 14 weeks 2. Depression is measured using the Geriatric Depression Scale (GDS) at baseline, 6, 10 and 14 weeks 3. Anxiety is measured using the Geriatric Depression Scale (GDS) at baseline, 6, 10 and 14 weeks

Countries

Malaysia

Contacts

Public ContactAzin Farzin
aizan@upm.edu.my+60 (0)1 128 059 793

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 5, 2026