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Long-term Effects of Interventional Strategies to Prevent Cognitive Decline in Elderly. (MAPT-PLUS)

Primary Purpose

Frail Elderly

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Gröber and Buschke test
Sponsored by
University Hospital, Toulouse
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Frail Elderly focused on measuring Cognitive decline, prevention, omega-3 fatty acids, nutrition exercise, cognitive training, social activities, frailty

Eligibility Criteria

70 Years - undefined (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

Subjects who meet the following criteria will be included in the MAPT PLUS study :

  • frail elderly subjects participating in the MAPT study and still followed at 3 years,
  • subjects capable of understanding the protocol, complying with its requirements and attending the follow-up visits proposed as part of the extended phase of the MAPT study,
  • subjects capable of giving their written informed consent and complying with the requirements of the study,
  • subjects covered by a health insurance system.

Exclusion Criteria:

Subjects who fulfill at least one of the following criteria will not be included in the MAPT PLUS study :

  • known presence of dementia or Alzheimer's disease (DSM IV criteria) diagnosed during the MAPT follow-up,
  • known presence of severe diseases that are life-threatening in the short term,
  • visual or hearing impairments that are incompatible with performance and/or interpretation of the neuropsychological tests,
  • history and/or presence of any disorder (severe depression or generalized anxiety) which, according to the investigator, is likely to interfere with the results of the study or to expose the subject to a supplementary risk,
  • participation in another clinical study during the period of the present study,
  • subjects who have refused cognitive evaluation during the MAPT follow-up,
  • subjects deprived of their freedom by administrative or judicial decision, or under guardianship,
  • with regard to performance of MRI: presence of a pacemaker or metallic materials, claustrophobia.

Sites / Locations

  • UH Toulouse - La Grave

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

Gröber and Buschke test

Outcomes

Primary Outcome Measures

Gröber and Buschke test (spontaneous delayed recall score)
Assessment of cognitive and functional performances according to the spontaneous delayed recall score(Gröber and Buschke test)
Cognitive and functional performance (Gröber and Buschke test-spontaneous delayed recall score)
Assessment of cognitive and functional performances by using the Gröber and Buschke test (spontaneous delayed recall score)at 5 years after the participation to the MAPT study.

Secondary Outcome Measures

MRI test
Evaluation of the long-term impact of MAPT study interventions on changes in markers of cerebral atrophy (overall brain volume of specific brain structures such as the hippocampus)
Cost-effectiveness Evaluation
Evaluation of the long-term impact of the MAPT interventions in terms of cost-effectiveness ratio by using a medico-economic data collection

Full Information

First Posted
December 30, 2011
Last Updated
August 24, 2020
Sponsor
University Hospital, Toulouse
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1. Study Identification

Unique Protocol Identification Number
NCT01513252
Brief Title
Long-term Effects of Interventional Strategies to Prevent Cognitive Decline in Elderly.
Acronym
MAPT-PLUS
Official Title
A 2-years Extension Study of MAPT Trial : Evaluation of the Long Term Effects of Interventional Strategies to Prevent the Decline in Cognitive Functioning in Frail Older Adults
Study Type
Interventional

2. Study Status

Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
December 2011 (Actual)
Primary Completion Date
April 15, 2016 (Actual)
Study Completion Date
July 20, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Toulouse

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The MAPT PLUS study is a two-year extension of follow-up of the patients included in the MAPT preventive study, after completion of the interventions. Subjects in the four groups of the MAPT study will be prospectively followed. MAPT is a multicentre, randomised, placebo-controlled study, using a 4-group design with 3 treatment groups (omega 3 alone, multi-domain intervention alone, omega 3 plus multi-domain intervention, n=420 each) and a placebo group (n=420). The MAPT PLUS study will be an extension of the MAPT study and includes an annual follow-up for two years.
Detailed Description
The MAPT PLUS study is a follow-up of subjects initially included in an interventional study. The follow-up that we propose in this request for funding does not involve any intervention, but aims to assess the long-term effect of the interventions previously carried out during the three years of the MAPT study. * Description of the interventions to which subjects are exposed during the first 3 years of follow-up (MAPT study) : In the MAPT study, subjects are randomized into 4 groups: V0137 CA group: 2 soft capsules of V0137 CA once a day (2 x 400 mg/day); Multi-domain intervention group (nutrition, physical activity, cognitive stimulation, social activities) + placebo, 2 soft capsules once a day ; Multi-domain intervention group (nutrition, physical activity, cognitive stimulation, social activities) + V0137 CA, 2 soft capsules once a day ; Placebo group: 2 soft capsules of placebo once a day. * Description of the multidomain intervention : The multi-domain intervention consists of collective training sessions and a yearly personalized preventive consultation which aims to detect risk factors (sensory disturbances, difficulty in walking, nutritional disturbances, vascular risk factors) and to set up management in collaboration with the general practitioner. The collective sessions take place in groups of 6 to 8 subjects. In the first month, two sessions a week are scheduled, and in the second month, one session a week. The first two months correspond to the intensive programme. Each session comprises 1 hour of cognitive training, 45 minutes of information on physical activity and 15 minutes of dietary advice. From the third month, sessions are held monthly and aim to consolidate the key messages and to stimulate adherence to the programme. The sessions are shorter (1 hour review of one of the domains of the intensive programme). " Booster " sessions (2 hours) are delivered at 12 and 24 months after the first sessions of the intensive programme. Twenty-minute individual interviews also take place every 6 months with the leader of the training sessions (6 interviews in the course of 3 years).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Frail Elderly
Keywords
Cognitive decline, prevention, omega-3 fatty acids, nutrition exercise, cognitive training, social activities, frailty

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
1028 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Gröber and Buschke test
Intervention Type
Behavioral
Intervention Name(s)
Gröber and Buschke test
Intervention Description
spontaneous delayed recall score after a 5 years follow-up
Primary Outcome Measure Information:
Title
Gröber and Buschke test (spontaneous delayed recall score)
Description
Assessment of cognitive and functional performances according to the spontaneous delayed recall score(Gröber and Buschke test)
Time Frame
2 years
Title
Cognitive and functional performance (Gröber and Buschke test-spontaneous delayed recall score)
Description
Assessment of cognitive and functional performances by using the Gröber and Buschke test (spontaneous delayed recall score)at 5 years after the participation to the MAPT study.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
MRI test
Description
Evaluation of the long-term impact of MAPT study interventions on changes in markers of cerebral atrophy (overall brain volume of specific brain structures such as the hippocampus)
Time Frame
2 years
Title
Cost-effectiveness Evaluation
Description
Evaluation of the long-term impact of the MAPT interventions in terms of cost-effectiveness ratio by using a medico-economic data collection
Time Frame
2 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Subjects who meet the following criteria will be included in the MAPT PLUS study : frail elderly subjects participating in the MAPT study and still followed at 3 years, subjects capable of understanding the protocol, complying with its requirements and attending the follow-up visits proposed as part of the extended phase of the MAPT study, subjects capable of giving their written informed consent and complying with the requirements of the study, subjects covered by a health insurance system. Exclusion Criteria: Subjects who fulfill at least one of the following criteria will not be included in the MAPT PLUS study : known presence of dementia or Alzheimer's disease (DSM IV criteria) diagnosed during the MAPT follow-up, known presence of severe diseases that are life-threatening in the short term, visual or hearing impairments that are incompatible with performance and/or interpretation of the neuropsychological tests, history and/or presence of any disorder (severe depression or generalized anxiety) which, according to the investigator, is likely to interfere with the results of the study or to expose the subject to a supplementary risk, participation in another clinical study during the period of the present study, subjects who have refused cognitive evaluation during the MAPT follow-up, subjects deprived of their freedom by administrative or judicial decision, or under guardianship, with regard to performance of MRI: presence of a pacemaker or metallic materials, claustrophobia.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bruno Vellas, MD
Organizational Affiliation
University Hospital, Toulouse
Official's Role
Principal Investigator
Facility Information:
Facility Name
UH Toulouse - La Grave
City
Toulouse
ZIP/Postal Code
31059
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
33666880
Citation
Takano E, Maltais M, Kondo I, Rolland Y; MAPT/DSA group. Bidirectional relationship between depressive symptoms and physical performance in community-dwelling older people with subjective memory complaints. Eur Geriatr Med. 2021 Oct;12(5):973-980. doi: 10.1007/s41999-021-00473-9. Epub 2021 Mar 5.
Results Reference
derived
PubMed Identifier
33076983
Citation
Delrieu J, Voisin T, Saint-Aubert L, Carrie I, Cantet C, Vellas B, Payoux P, Andrieu S. The impact of a multi-domain intervention on cerebral glucose metabolism: analysis from the randomized ancillary FDG PET MAPT trial. Alzheimers Res Ther. 2020 Oct 19;12(1):134. doi: 10.1186/s13195-020-00683-6.
Results Reference
derived
PubMed Identifier
31558366
Citation
Delrieu J, Payoux P, Carrie I, Cantet C, Weiner M, Vellas B, Andrieu S. Multidomain intervention and/or omega-3 in nondemented elderly subjects according to amyloid status. Alzheimers Dement. 2019 Nov;15(11):1392-1401. doi: 10.1016/j.jalz.2019.07.008. Epub 2019 Sep 23.
Results Reference
derived
PubMed Identifier
30498824
Citation
Pothier K, de Souto Barreto P, Maltais M, Rolland Y, Vellas B. Shifting from Declines to Improvements: Associations between a Meaningful Walking Speed Change and Cognitive Evolution over Three Years in Older Adults. J Nutr Health Aging. 2018;22(10):1183-1188. doi: 10.1007/s12603-018-1059-8.
Results Reference
derived
PubMed Identifier
30207586
Citation
Lilamand M, Cesari M, Cantet C, Payoux P, Andrieu S, Vellas B; the MAPT/DSA study group. Relationship Between Brain Amyloid Deposition and Instrumental Activities of Daily Living in Older Adults: A Longitudinal Study from the Multidomain Alzheimer Prevention Trial. J Am Geriatr Soc. 2018 Oct;66(10):1940-1947. doi: 10.1111/jgs.15497. Epub 2018 Sep 12.
Results Reference
derived

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Long-term Effects of Interventional Strategies to Prevent Cognitive Decline in Elderly.

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