search
Back to results

Impact of Physical Activity on Successful Aging

Primary Purpose

Alzheimer Disease, Cognitive Impairment, Physical Activity

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Physical activity (PA)
cognitive treatment (CT)
Sponsored by
Universita di Verona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alzheimer Disease focused on measuring alzheimer's disease, physical activity, cognitive training

Eligibility Criteria

65 Years - 90 Years (Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • age ≥ 65 years;
  • Mini Mental State Examination (MMSE) ≥ 8;
  • Performance Oriented Mobility Assessment ≥ 19 (POMA).

Exclusion Criteria:

  • presence of other concurrent neurological diseases;
  • presence of other orthopaedic diseases involving the lower limbs and/or interfering with standing position and/or walking;
  • presence of severe auditory and visual deficits not corrected;
  • abuse of alcohol or drugs;
  • psychiatric disorders,
  • severe behavioral disorders;
  • hearth and respiratory disease that interfere with the motor activity.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm 4

    Arm Type

    Experimental

    Experimental

    No Intervention

    No Intervention

    Arm Label

    Alzheimer's Disease (G1)

    Alzheimer's Disease (G2)

    Healthy Old Subjects (G1)

    Healthy young Subjects (G2)

    Arm Description

    (G1) physical activity (PA)

    (G2) cognitive treatment (CT)

    Control group old

    Control group young

    Outcomes

    Primary Outcome Measures

    Mini Mental State Examination

    Secondary Outcome Measures

    Trail Making Test
    For MCI patients (Reitan,1958)
    Rivermead Behavioral Memory Test
    For MCI patients (Wilson, 1989)
    Tower of London
    For MCI patients (Shallice, 1982)
    Dual Task
    For MCI patients (Della Sala et al., 1997)
    Frontal Assessment Battery
    (Iavarone A et al., 2004)
    Attention Matrix
    For AD patients (Spinnler et al., 1987)
    Alzheimer's Disease Assessment Scale
    For AD patients (Rosen WG et al., 1984)
    6-Minute Walking Test
    (Ries JD et al., 2009)
    gait analysis by GAITRite® System
    (Bilney B et al., 2003)
    stabilometric assessments with Stability Line
    (Nashner LM and Peters JF, 1990),
    Instrumental Activity in Daily Living Scale (IADL)
    Neuropsychiatric Inventory Scale (NPI)
    cerebral circulation
    measured MRI arterial spin labeling
    peripheral vascular function
    measured by vascular doppler

    Full Information

    First Posted
    January 10, 2017
    Last Updated
    January 27, 2017
    Sponsor
    Universita di Verona
    search

    1. Study Identification

    Unique Protocol Identification Number
    NCT03034746
    Brief Title
    Impact of Physical Activity on Successful Aging
    Official Title
    Impact of Physical Activity on Successful Aging: Multidisciplinary Analysis of Mechanisms and Outcomes
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2017
    Overall Recruitment Status
    Completed
    Study Start Date
    September 2013 (undefined)
    Primary Completion Date
    May 2016 (Actual)
    Study Completion Date
    October 2016 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Universita di Verona

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Emerging literature suggests that vascular factors might be involved in the pathogenesis of Alzheimer's disease (AD). Other recent studies demonstrate the positive effects of physical activity on cognitive and behavioral disturbances of patients with AD. Therefore, it has been postulated that exercise enchantment in cerebral circulation is the physiological mechanism that link physical exercise and reduction of AD symptoms. Consequently, a program of physical activity could be considered one approach to counteract dementia by improving cerebrovascular health. However at this moment, it is not clear if the progressive brain vascular dysfunction and hypoperfusion, associated with the β-amyloid deposition, might be reversed or stabilized by an exercise intervention. The aim of this study is to assess, in patients with AD, the influence of physical exercise, compared to cognitive stimulation, on: Cognitive function; Independence in daily living and behavioral symptoms; Vascular function Finally, to investigate the physiological processes on the basis of the motor parameters' changes, the performances of the patients will be compared with the performances of healthy young and old subjects. MAIN OBJECTIVE: Investigate, in patients with Mild Cognitive Impairment (MCI) and AD, the effects of a physical activity program, or cognitive stimulation on global cognitive function. SECONDARY OBJECTIVES: Investigate the effects of the two treatments on: cognitive and motor performances, independence in activities of daily living, behavioral symptoms, peripheral vascular function.
    Detailed Description
    STUDY DESIGN: Randomised controlled, blinded clinical trial. SUBJECTS: The study will include 120 patients with definite diagnosis of MCI or AD and 30 young healthy subjects and 30 old healthy subjects referred to the Research Unit associated with the Department. Patients will be regarded as suitable to participate if they fulfilled the following criteria: Mini Mental State Examination (MMSE) ≥ 8; Performance Oriented Mobility Assessment ≥ 19 (POMA). Exclusion criteria will be: presence of other concurrent neurological diseases; presence of other orthopaedic diseases involving the lower limbs and/or interfering with standing position and/or walking; presence of severe auditory and visual deficits not corrected; abuse of alcohol or drugs; psychiatric disorders, severe behavioral disorders; hearth and respiratory disease that interfere with the motor activity. The protocol was be approved by the local ethics committee with number 2389. All participants will perform a physiatric examination by a medical doctor of the Department of Neurological and Movement Sciences. Written inform consent will be obtained from all participants before inclusion in the study. Participants who will meet the inclusion criteria will conduct a clinical and instrumental evaluation at enrollment (T0) and after 6 months ± 15 days after the first visit (T1). The assessment procedures will also be repeated after 3 months (T2) from T1. ASSESSMENT PROCEDURES Primary endpoints: - score obtained in the Mini Mental State Examination. Secondary endpoints: - score obtained in a cognitive battery. For MCI patients will be used: Trial Making Test (Reitan,1958), Rivermead Behavioral Memory Test (Wilson, 1989), Tower of London (Shallice, 1982), Dual Task (Della Sala et al., 1997), Frontal Assessment Battery (Iavarone A et al., 2004). For AD patients will be used: Attention Matrix (Spinnler et al., 1987), Alzheimer's Disease Assessment Scale (Rosen WG et al., 1984), Frontal Assessment Battery (Iavarone A et al., 2004). - score obtained in a motor skills assessment composed by: 6-Minute Walking Test (Ries JD et al., 2009), gait analysis by GAITRite® System (Bilney B et al., 2003), stabilometric assessments with Stability Line (Nashner LM and Peters JF, 1990), score obtained in the test Instrumental Activity in Daily Living (Lawton MP and Brody EM, 1969), score obtained in the test Neuropsychiatric Inventory (Cummings JL et al., 1994), peripheral vascular function measured by doppler. To evaluate the effectiveness of motor treatment, compared to a cognitive treatment on motor skills, cognitive skills, behavioral and autonomy in patients with cognitive decline, all patients will be evaluated by motor, cognitive, behavioral and autonomy scales, at baseline, after 6 months (T1), and after others 3 months (T2). A subgroup of 50% of patients will undergo instrumental procedures to investigate the effects of treatments on cerebral blood flow (arterial spin labeling). TREATMENT PROCEDURES The participants will be recruited and randomly assigned, according to the degree of cognitive decline, to one of the 3 groups (7-8 subjects): Physical Activity group (PA group): It will perform a program consist of 15 min of warm-up, 60 min of aerobic and resistance training, and 15 min of cool-down. Cognitive treatment group (CT group): The cognitive stimulation group will received a rehabilitation program with multimodal repetitive stimulation in order to exercise and reinforce the cognitive skills of the participant to slow/prevent the decline. In particular the treatment will be focused on reorient the patient about his/her-self, his/her history and his/her environment, to improve the memory skill by teaching compensatory and restitutive strategies, to help the patient to the discussion about everyday life and in particular to the everyday problems The PA and CT groups will be homogeneous for clinical and demographic data, and participants will undergo 72 treatment group sessions, 60-minute/session, and 3 days/week for 6 consecutively months. Both types of treatment will be balanced with different degrees of difficulty depending on the state of disease severity . o The control groups (CG) will not receive any such treatment during the study and they will be evaluated by the same clinical and instrumental assessments.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Alzheimer Disease, Cognitive Impairment, Physical Activity
    Keywords
    alzheimer's disease, physical activity, cognitive training

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    Outcomes Assessor
    Allocation
    Randomized
    Enrollment
    90 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Alzheimer's Disease (G1)
    Arm Type
    Experimental
    Arm Description
    (G1) physical activity (PA)
    Arm Title
    Alzheimer's Disease (G2)
    Arm Type
    Experimental
    Arm Description
    (G2) cognitive treatment (CT)
    Arm Title
    Healthy Old Subjects (G1)
    Arm Type
    No Intervention
    Arm Description
    Control group old
    Arm Title
    Healthy young Subjects (G2)
    Arm Type
    No Intervention
    Arm Description
    Control group young
    Intervention Type
    Other
    Intervention Name(s)
    Physical activity (PA)
    Intervention Description
    It will perform a program consist of 15 min of warm-up, 60 min of aerobic and resistance training, and 15 min of cool-down.
    Intervention Type
    Other
    Intervention Name(s)
    cognitive treatment (CT)
    Intervention Description
    The cognitive stimulation group will received a rehabilitation program with multimodal repetitive stimulation in order to exercise and reinforce the cognitive skills of the participant to slow/prevent the decline. In particular the treatment will be focused on reorient the patient about his/her-self, his/her history and his/her environment, to improve the memory skill by teaching compensatory and restitutive strategies, to help the patient to the discussion about everyday life and in particular to the everyday problems
    Primary Outcome Measure Information:
    Title
    Mini Mental State Examination
    Time Frame
    0-6-9 months (change will be assessed)
    Secondary Outcome Measure Information:
    Title
    Trail Making Test
    Description
    For MCI patients (Reitan,1958)
    Time Frame
    0-6-9 months (change will be assessed)
    Title
    Rivermead Behavioral Memory Test
    Description
    For MCI patients (Wilson, 1989)
    Time Frame
    0-6-9 months (change will be assessed)
    Title
    Tower of London
    Description
    For MCI patients (Shallice, 1982)
    Time Frame
    0-6-9 months (change will be assessed)
    Title
    Dual Task
    Description
    For MCI patients (Della Sala et al., 1997)
    Time Frame
    0-6-9 months (change will be assessed)
    Title
    Frontal Assessment Battery
    Description
    (Iavarone A et al., 2004)
    Time Frame
    0-6-9 months (change will be assessed)
    Title
    Attention Matrix
    Description
    For AD patients (Spinnler et al., 1987)
    Time Frame
    0-6-9 months (change will be assessed)
    Title
    Alzheimer's Disease Assessment Scale
    Description
    For AD patients (Rosen WG et al., 1984)
    Time Frame
    0-6-9 months (change will be assessed)
    Title
    6-Minute Walking Test
    Description
    (Ries JD et al., 2009)
    Time Frame
    0-6-9 months (change will be assessed)
    Title
    gait analysis by GAITRite® System
    Description
    (Bilney B et al., 2003)
    Time Frame
    0-6-9 months (change will be assessed)
    Title
    stabilometric assessments with Stability Line
    Description
    (Nashner LM and Peters JF, 1990),
    Time Frame
    0-6-9 months (change will be assessed)
    Title
    Instrumental Activity in Daily Living Scale (IADL)
    Time Frame
    0-6-9 months (change will be assessed)
    Title
    Neuropsychiatric Inventory Scale (NPI)
    Time Frame
    0-6-9 months (change will be assessed)
    Title
    cerebral circulation
    Description
    measured MRI arterial spin labeling
    Time Frame
    0-6-9 months (change will be assessed)
    Title
    peripheral vascular function
    Description
    measured by vascular doppler
    Time Frame
    0-6-9 months (change will be assessed)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    65 Years
    Maximum Age & Unit of Time
    90 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: age ≥ 65 years; Mini Mental State Examination (MMSE) ≥ 8; Performance Oriented Mobility Assessment ≥ 19 (POMA). Exclusion Criteria: presence of other concurrent neurological diseases; presence of other orthopaedic diseases involving the lower limbs and/or interfering with standing position and/or walking; presence of severe auditory and visual deficits not corrected; abuse of alcohol or drugs; psychiatric disorders, severe behavioral disorders; hearth and respiratory disease that interfere with the motor activity.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Nicola Smania
    Organizational Affiliation
    Department of Neurological and Movement Sciences
    Official's Role
    Study Chair
    First Name & Middle Initial & Last Name & Degree
    Federico Schena
    Organizational Affiliation
    Department of Neurological and Movement Sciences
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No
    Citations:
    PubMed Identifier
    20209421
    Citation
    Venturelli M, Lanza M, Muti E, Schena F. Positive effects of physical training in activity of daily living-dependent older adults. Exp Aging Res. 2010 Apr;36(2):190-205. doi: 10.1080/03610731003613771.
    Results Reference
    result
    PubMed Identifier
    21852281
    Citation
    Venturelli M, Scarsini R, Schena F. Six-month walking program changes cognitive and ADL performance in patients with Alzheimer. Am J Alzheimers Dis Other Demen. 2011 Aug;26(5):381-8. doi: 10.1177/1533317511418956. Epub 2011 Aug 17.
    Results Reference
    result
    PubMed Identifier
    22984089
    Citation
    Venturelli M, Magalini A, Scarsini R, Schena F. From Alzheimer's disease retrogenesis: a new care strategy for patients with advanced dementia. Am J Alzheimers Dis Other Demen. 2012 Nov;27(7):483-9. doi: 10.1177/1533317512459794. Epub 2012 Sep 13.
    Results Reference
    result
    PubMed Identifier
    24219216
    Citation
    Venturelli M, Scarsini R, Muti E, Salvagno GL, Schena F. Sundowning syndrome and hypothalamic-pituitary-adrenal axis dysregulation in individuals with Alzheimer's disease: is there an association? J Am Geriatr Soc. 2013 Nov;61(11):2055-6. doi: 10.1111/jgs.12491. No abstract available.
    Results Reference
    result
    PubMed Identifier
    27347878
    Citation
    Venturelli M, Ce E, Limonta E, Muti E, Scarsini R, Brasioli A, Schena F, Esposito F. Possible Predictors of Involuntary Weight Loss in Patients with Alzheimer's Disease. PLoS One. 2016 Jun 27;11(6):e0157384. doi: 10.1371/journal.pone.0157384. eCollection 2016.
    Results Reference
    result
    PubMed Identifier
    27540967
    Citation
    Venturelli M, Sollima A, Ce E, Limonta E, Bisconti AV, Brasioli A, Muti E, Esposito F. Effectiveness of Exercise- and Cognitive-Based Treatments on Salivary Cortisol Levels and Sundowning Syndrome Symptoms in Patients with Alzheimer's Disease. J Alzheimers Dis. 2016 Jul 14;53(4):1631-40. doi: 10.3233/JAD-160392.
    Results Reference
    result
    PubMed Identifier
    27802234
    Citation
    Crispoltoni L, Stabile AM, Pistilli A, Venturelli M, Cerulli G, Fonte C, Smania N, Schena F, Rende M. Changes in Plasma beta-NGF and Its Receptors Expression on Peripheral Blood Monocytes During Alzheimer's Disease Progression. J Alzheimers Dis. 2017;55(3):1005-1017. doi: 10.3233/JAD-160625.
    Results Reference
    result
    PubMed Identifier
    30744116
    Citation
    Pedrinolla A, Venturelli M, Tamburin S, Fonte C, Stabile AM, Galazzo IB, Ghinassi B, Venneri MA, Pizzini FB, Muti E, Smania N, Di Baldassarre A, Naro F, Rende M, Schena F. Non-Abeta-Dependent Factors Associated with Global Cognitive and Physical Function in Alzheimer's Disease: A Pilot Multivariate Analysis. J Clin Med. 2019 Feb 9;8(2):224. doi: 10.3390/jcm8020224.
    Results Reference
    derived
    PubMed Identifier
    29376858
    Citation
    Pedrinolla A, Venturelli M, Fonte C, Munari D, Benetti MV, Rudi D, Tamburin S, Muti E, Zanolla L, Smania N, Schena F. Exercise Training on Locomotion in Patients with Alzheimer's Disease: A Feasibility Study. J Alzheimers Dis. 2018;61(4):1599-1609. doi: 10.3233/JAD-170625.
    Results Reference
    derived

    Learn more about this trial

    Impact of Physical Activity on Successful Aging

    We'll reach out to this number within 24 hrs