Memory Encoding Strategies for People With Mild Cognitive Impairments

Sponsor
University of Western Sydney (Other)
Overall Status
Completed
CT.gov ID
NCT02953964
Collaborator
(none)
60
2
3
65
30
0.5

Study Details

Study Description

Brief Summary

The purposes of the study are:
  • To evaluate the effectiveness of a perceptual-based training program in enhancing cognitive and everyday functioning of older adults with mild cognitive impairment and mild dementia

  • To evaluate the effectiveness of a semantic-based training program in enhancing cognitive and everyday functioning of older adults with mild cognitive impairment and mild dementia

Condition or Disease Intervention/Treatment Phase
  • Other: Behavioral: perceptual-based memory encoding training
  • Other: Behavioral: semantic-based memory encoding training
  • Other: Behavioral: Cognitive stimulation group (control group)
N/A

Detailed Description

People with dementia experience a cognitive decline that affects their functional performance. It has been identified that encoding is less effective in people with dementia. Rehabilitating at the encoding stage is, therefore, essential. A recent systematic review found that effective interventions needed to include training in individually selected memory encoding strategies. These strategies are classified as either perceptual (visual) or semantic (association) memory encoding strategies.

Based on the above literature, the chief investigator (Associate Professor Karen Liu) ran a pilot study on an integrated home and community centre cognitive training programme for 20 elderly people with memory problem using a pre-test and post-test comparison design.

Extending on the positive results, the aim of this project was to investigate the effectiveness of perceptual and semantic encoding strategies (and compare with a control intervention). It also aims to promote the understanding of memory loss and dementia and the need for early intervention for family members of the participants.

Study Design

Study Type:
Interventional
Actual Enrollment :
60 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Perceptual and Semantic Memory Encoding Strategies for People With Mild Cognitive Impairment
Study Start Date :
May 1, 2010
Actual Primary Completion Date :
Oct 1, 2015
Actual Study Completion Date :
Oct 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Experimental: Behavioral: perceptual-based memory encoding training

Participants receive perceptual-based memory encoding training

Other: Behavioral: perceptual-based memory encoding training
Participants are trained in the use of perceptual-based memory encoding strategies, inclusive of visual imagery and the method of loci. Visual imagery involves the creation and encoding of mental images, while the method of loci refers to linking these images with specific places to facilitate memory (Simon et al., 2012). Participants are taught to visualise performing each step of a task in a familiar environment, such as in their home (Liu et al., 2009). After participants can correctly visualise the entire task, they then progress to actually performing the task. During the intervention sessions, 2-3 tasks are covered each session, and these tasks become progressively difficult as the weeks progress. The intervention lasts for 10 weeks with one session every week. Each session runs for 90 minutes. A follow-up home training program is run once a week for 30 minutes with the participant and their care-giver.

Experimental: Behavioral: Semantic-based memory encoding training

Participants receive semantic-based memory encoding training

Other: Behavioral: semantic-based memory encoding training
Participants are asked to encode the steps of a task by forming an association of the steps and sequence. Participants are trained in the use of the chunking association method and honeycomb concept and perform different tasks each week, implementing this encoding strategy (Lim et al., 2012). The chunking association method breaks down information into smaller parts and helps with the encoding and retrieval of information. The honeycomb concept allows the steps to form a story in relation to place, time, characters, problem and solution and the story is verbalised. Participants then complete the task. During the intervention sessions, 2-3 tasks are covered each session, and these tasks become progressively difficult as the weeks progress. The intervention lasts for 10 weeks with one session every week. Each session runs for 90 minutes. A follow-up home training program is run once a week for 30 minutes with the participant and their care-giver.

Active Comparator: Behavioral : control group

Participants receive cognitive stimulation intervention

Other: Behavioral: Cognitive stimulation group (control group)
Participants receiving cognitive stimulation intervention. It consists of eight sessions that train participants' visual attention and memory, auditory attention and memory and their application in daily activities. Two sessions are also given which allow for participants to apply the training practically in their daily lives. The intervention lasts for 10 weeks with one session every week. Each session runs for 90 minutes. A follow-up home training program is run once a week for 30 minutes with the participant and their care-giver.
Other Names:
  • Cognitive stimulation group
  • Outcome Measures

    Primary Outcome Measures

    1. Change in Disability Assessment for Dementia [Within two days before the intervention and within two days after the 10-week intervention]

      Change in Disability Assessment for Dementia to assess assistance required in basic daily tasks such as dressing, bathing

    2. Change in Instrumental Activities of Daily Living Scale [Within two days before the intervention and within two days after the 10-week intervention]

      Change in Instrumental Activities of Daily Living Scale to assess assistance required in instrumental daily tasks such as laundry, meal preparation

    Secondary Outcome Measures

    1. Change in Cognistat [Within two days before the intervention and within two days after the 10-week intervention]

      Change in Cognistat to assess general cognitive function

    2. Change in Digit Span Test [Within two days before the intervention and within two days after the 10-week intervention]

      Change in Digit Span Test to assess attention and working memory

    3. Change in Consortium to Establish a Registry for Alzheimer's Disease [Within two days before the intervention and within two days after the 10-week intervention]

      Change in Consortium to Establish a Registry for Alzheimer's Disease to assess cognitive function in verbal fluency, memory

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    60 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Selection Criteria:
    • are aged 60 or above;

    • have no previous psychiatric or memory disorder history or other neurological illness;

    • have Mini-mental State Examination score (MMSE) greater than or equal to 21;

    • have Clinical Dementia Rating score (CDR) of 0.5 or 1 indicating very mild and mild dementia;

    • do not show sign of depression with score below 9 out of 30 in the Geriatric Depression Scale;

    • are able to communicate effectively;

    • have family member who can participate in the study; and

    • voluntarily consent to participate in the study.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Western Sydney University Penrith New South Wales Australia 2751
    2 The Hong Kong Polytechnic University Hong Kong Hong Kong

    Sponsors and Collaborators

    • University of Western Sydney

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Karen Liu, Associate Professor, University of Western Sydney
    ClinicalTrials.gov Identifier:
    NCT02953964
    Other Study ID Numbers:
    • Memory encoding
    First Posted:
    Nov 3, 2016
    Last Update Posted:
    Nov 3, 2016
    Last Verified:
    Nov 1, 2016
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 3, 2016