Measuring the Impact of Cognitive and Psychosocial Interventions in Persons With Mild Cognitive Impairment
Memory interventions are training programs that provide a variety of cognitive and psychological strategies meant to improve memory. These interventions have been shown to yield significant benefits to normal aged persons and small-size studies have shown that they are suitable and beneficial for persons with mild cognitive impairment. The goal of this proposal is to assess with a well-controlled design the efficiency and specificity of cognitive training in persons with mild cognitive impairment.
The hypothesis is that cognitive training can improve the cognition of persons with mild cognitive impairment and that this improvement can be enduring.
Mild Cognitive Impairment
Other: Cognitive intervention
Other: Psychosocial intervention
|Study Design:||Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Treatment
|Official Title:||Measuring the Impact of Cognitive and Psychosocial Interventions in Persons With Mild Cognitive Impairment|
- Change in memory measures [ Time Frame: one week before and after intervention, and three and six months later ] [ Designated as safety issue: No ]Unrelated word list learning and Face-name memory tests
- generalization of therapeutic gains to everyday life [ Time Frame: one week before and after intervention, and three and six months later ] [ Designated as safety issue: No ]Self-Evaluation Complaints Questionnaire, Activities of Daily Living- Prevention Instrument questionnaire, Multifactorial Memory Questionnaire tests and participants will be asked to press a button to record each occasion when they use a strategy in their daily lives.
- Change in psychological health measures [ Time Frame: one week before and after intervention, and 3 and 6 months later ] [ Designated as safety issue: No ]geriatric anxiety inventory, griatric depression scale and general well-being schedule tests
|Study Start Date:||November 2011|
|Estimated Study Completion Date:||January 2016|
|Estimated Primary Completion Date:||December 2015 (Final data collection date for primary outcome measure)|
Experimental: Cognitive intervention
Use of Memo protocol for 8 weeks
Other: Cognitive intervention
Different strategies will be included to improve episodic memory. Training on imagery will be provided prior to episodic training.Particular attention will be paid to memory self-efficacy and the negative perception that elderly individuals entertain about memory tasks. The issue of generalization is of major importance in cognitive therapy.
Experimental: Psychosocial intervention
Use of "Programme d'intervention psychosociale axé sur le bien-être psychologique" for 8 weeks
Other: Psychosocial intervention
Based on a cognitive-behavioural approach, the psychosocial intervention will aim at improving general psychological well-being or preventing psychological distress in persons with MCI.
No Intervention: no contact control group
Elderly persons with mild cognitive impairment experience a cognitive decline that is confirmed by a neuropsychological examination but do not meet the clinical criteria for dementia. However, longitudinal studies have shown that up to 75% of these persons develop dementia of the Alzheimer type after 5 years of follow-up. A significant proportion of these persons are thus in a prodromal phase of the disease. This phase is likely to represent a key moment in which to apply appropriate interventions. Indeed, these persons have the cognitive capabilities to benefit from such interventions. Cognitive training has been shown to be effective in improving the memory function of older persons without cognitive decline and increasing evidence indicates that persons with MCI might also benefit from such interventions. However, there is few researches have focused on the Mild Cognitive Impairment population in spite of the fact that they are at-risk of experiencing significant cognitive problems in the next few years while still having the potential to benefit from non-pharmacological interventions. In a number of pilot studies, the investigators compared cognitive and psychosocial intervention to a control intervention in persons with MCI. The participants' performance improved on proximal outcomes and on distal outcomes (activities of daily living). The purpose of this project is to study the efficacy of the cognitive intervention in a larger group of participants, compare it with a non-cognitive intervention, assess the long term maintenance of the improvement and measure the potential implication of cognitive and psychosocial factors.
Persons with Mild Cognitive Impairment will first receive a comprehensive clinical assessment to determine whether they meet the research criteria for Mild Cognitive Impairment. They will then be randomly allocated to one of three groups. One group will receive cognitive training, one group will receive psychosocial intervention and one group will receive no intervention. The two interventions will be offered on a one-session per week basis during an 8-week period. The cognitive intervention will include training of attention and episodic memory. This intervention is based on recently acquired knowledge regarding the nature of the deficits in mild cognitive impairment as well as factors that are known to optimize memory. The psychosocial intervention will focus on goal management. Booster sessions will be offered to the intervention groups after 3 and 6 months. Each intervention will act as social contact control group for the other intervention. The third group will receive no intervention and will be used as a no-contact control group.
All groups will undergo one pre-intervention assessment (1-2 week before beginning of intervention), one post-intervention assessment (1-2 week after end of intervention) and additional assessments one week after before the booster sessions and nine month following end of training. This last assessment will measure long-term retention of training and will assess the degree of change in the clinical profile of patients.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01448148
|Contact: Emilie Lepage, M.Sc.||514-340-3540 ext email@example.com|
|Contact: Samira Mellah, Ph.D.||514-340-3540 ext firstname.lastname@example.org|
|Centre de recherche de l'Institut universitaire de geriatrie de Montreal||Recruiting|
|Montreal, Quebec, Canada, H3W 1W5|
|Contact: Émilie Lepage, M.Sc. 514-340-3540 ext 4710 email@example.com|
|Principal Investigator: Sylvie Belleville, Ph.D.|
|Centre hospitalier Robert-Giffard||Recruiting|
|Quebec, Canada, G1J 2G3|
|Contact: Carol Hudon, Ph.D. 418-656-2131 ext 3745 firstname.lastname@example.org|
|Principal Investigator: Carol Hudon, Ph.D.|
|Principal Investigator:||Sylvie Belleville, Ph.D.||Centre de recherche Institut universitaire de geriatrie de Montreal|
|Study Director:||Carol Hudon, Ph.D.||Laval University, Psychology department|