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Exercise the Mind and Brain. A Multimodal Intervention in Stroke (Mindfit)

Primary Purpose

Stroke

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Multicomponent Physical Activity Program
Mindfulness-Based Stress Reduction Program
Computerized Cognitive Training
Sponsored by
University of Barcelona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring Neuroplasticity, stroke, neuroprotection, physical exercise, cognitive training, mindfulness, neuroimaging, intervention, randomization, blind

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Individuals aged 18-80 years old
  • Ischemic or hemorrhagic stroke
  • Stroke diagnoses between 3-60 months ago
  • To have consent from a physician to engage in an exercise intervention
  • Fluency in Catalan or Spanish (I.e., able to understand and speak)
  • Accept to take part in the study and sign the informed consent according to the Declaration of Helsinki.

Exclusion Criteria:

  • Cognitive impairment (MMSE > 23)
  • Severe aphasia (item 9 of the NIHSS scale ≥ 2)
  • Severe sensory problems
  • Other neurological conditions apart from stroke
  • Severe pre-stroke psychiatric disorders (e.g., bipolar disorder, schizophrenia)
  • History of alcohol or other toxic abuse

Exclusion criteria only for MRI examination:

  • Claustrophobia
  • Medical device (e.g., pacemaker implants, stents)
  • Other metal objects in the body

Sites / Locations

  • Maria Mataro

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Physical exercise & cognitive training group

Mindfulness & cognitive training group

Cognitive training group

Arm Description

The Physical exercise & cognitive training group receives a multicomponent physical exercise program combined with computer-based cognitive training.

The Mindfulness & cognitive training group receives mindfulness-based stress reduction therapy combined with computer-based cognitive training.

The Cognitive training group, as an active control group, receives only computer-based cognitive training.

Outcomes

Primary Outcome Measures

Change in immediate verbal attention after receiving treatment
Forward Digit Span (WAIS III)
Change in verbal digit working memory after receiving treatment
Backward Digit Span (WAIS III)
Change in verbal memory after receiving treatment
Rey Auditory Learning Test
Change in visual memory after receiving treatment
Rey's Complex Figure Test
Change in executive function, verbal fluency after receiving treatment
Phonetic Fluency is measured using the Controlled Oral Word Association Test, spanish adaptation, and semantic fluency test using the category Animal
Change in executive function, inhibition after receiving treatment
Stroop Test
Change in executive function, set-switching task after receiving treatment
Trail Making Test
Change in language, naming after receiving treatment
Boston naming Test

Secondary Outcome Measures

Changes in psychological distress
Clinical Outcomes in Routine Evaluation (CORE-OM)
Changes in depression and anxiety
Depression Anxiety Stress Scale (DASS-21)
Changes in wellbeing
Ryff Scales of Psychological Wellbeing.
Changes in Mindfulness
Mindful Attention Awareness Scale (MAAS)
Changes in White matter integrity
White matter integrity: tractography
Changes in Resting-state connectivity
Resting state brain activity using fMRI
Changes in brain volumetry
Grey and white matter volume measured by MRI
Molecular changes: growth factors (BDNF, SDF1-a, VEGF-A, IGF-1, and NGF), cortisol, protein C reactive, IL-6 and homocysteine levels
Quantification of different biomarkers from blood samples.
Changes in Microbiota data
Bacterial composition of stool samples in terms of relative abundance
Changes in Sleep
Pittsburgh Sleep Quality Index (PSQI)
Changes in Fitness
Senior Fitness Test (SFT)
Changes in stroke specific quality of life
Stroke-specific Quality of Life Scale (ECVI-38)
Changes in quality of life
World Health Organization Quality of Life (WHOQOL-BREF)
Changes in mental fatigue
Fatigue Assessment Scale (FAS)
Changes in physical activity:
Spanish version of the reduced Minnesota leisure-time physical and activity questionnaire (VREM)

Full Information

First Posted
December 31, 2020
Last Updated
March 1, 2022
Sponsor
University of Barcelona
Collaborators
Fundació La Marató de TV3, Germans Trias i Pujol Hospital, Institut Guttmann, Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina, University of Pittsburgh
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1. Study Identification

Unique Protocol Identification Number
NCT04759950
Brief Title
Exercise the Mind and Brain. A Multimodal Intervention in Stroke
Acronym
Mindfit
Official Title
Effects of Combined Therapies of Physical Exercise, Mindfulness and Cognitive Stimulation on Cognition and Neuroplasticity in Chronic Stroke Patients: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
March 2022
Overall Recruitment Status
Completed
Study Start Date
October 28, 2020 (Actual)
Primary Completion Date
July 30, 2021 (Actual)
Study Completion Date
January 30, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Barcelona
Collaborators
Fundació La Marató de TV3, Germans Trias i Pujol Hospital, Institut Guttmann, Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina, University of Pittsburgh

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The main objective of MindFit Project is to develop an evidence-based multimodal investigation of combined non-pharmacological strategies in chronic stroke patients and clarify the neuroplasticity mechanisms underlying the benefits of physical exercise and mindfulness strategies combined with cognitive training on post-stroke recovery. The investigators have adopted a multidisciplinary and multimodal approach to provide a more integrative perspective using cognitive, social-psychological, biochemical, and neuroimaging measurements.
Detailed Description
The MindFit Project is a multicentric, prospective, parallel, single-blinded, randomized controlled trial with a sample of 141 participants at 3 to 60 months after stroke. Participants are randomly allocated to one of three arms (through a simple randomizing procedure with a 1:1:1 ratio created with a random sequence generator software). The first group (n=47) receives computer-based cognitive training (CCT) combined with a multicomponent physical exercise program. The second group (n=47) receives CCT combined with mindfulness-based stress reduction therapy. Finally, the third group (n=47), as an active control group, receives only CCT. All interventions last 12 weeks. Within two weeks before the start of the interventions, and again at 3 months after completing the interventions, medical, cognitive, and physical assessments, neuroimaging, and biological samples collection are performed. The objectives of this project are: To examine the effects of multimodal interventions in a population of chronic stroke patients on various domains: cognition, emotion, physical health, and quality of life. To examine specific plasticity effects of each of the three interventions regarding structural and functional magnetic resonance imaging (MRI) and how these changes may contribute to cognitive and emotional benefits. To study the molecular mechanisms by which the different types of interventions influence cognitive, emotional and brain benefits. To study interventions-induced microbiome changes and to explain how these changes may induce inflammatory and immune responses that may contribute to cognitive, emotional and brain benefits. To determine the demographic, clinical and genetic factors that may modulate cognitive, emotional and brain changes: baseline cognitive status; baseline cerebral status (atrophy, total intracranial volume); sex; age, educational level, intelligence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke
Keywords
Neuroplasticity, stroke, neuroprotection, physical exercise, cognitive training, mindfulness, neuroimaging, intervention, randomization, blind

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
141 participants at 3 to 60 months after stroke are randomly allocated to one of three arms: The first group (n=47) receives computer-based cognitive training (CCT) combined with a multicomponent physical exercise program. The second group (n=47) receives CCT combined with mindfulness-based stress reduction therapy. Finally, the third group (n=47), as an active control group, receives only CCT.
Masking
InvestigatorOutcomes Assessor
Masking Description
The randomization sequence is concealed (blinded) from research personnel, so that the investigators are not aware of whether a particular subject has been randomized to one of the intervention groups or to the active control group.
Allocation
Randomized
Enrollment
141 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Physical exercise & cognitive training group
Arm Type
Experimental
Arm Description
The Physical exercise & cognitive training group receives a multicomponent physical exercise program combined with computer-based cognitive training.
Arm Title
Mindfulness & cognitive training group
Arm Type
Experimental
Arm Description
The Mindfulness & cognitive training group receives mindfulness-based stress reduction therapy combined with computer-based cognitive training.
Arm Title
Cognitive training group
Arm Type
Active Comparator
Arm Description
The Cognitive training group, as an active control group, receives only computer-based cognitive training.
Intervention Type
Behavioral
Intervention Name(s)
Multicomponent Physical Activity Program
Intervention Description
The proposed physical exercise intervention follows the American College of Sports Medicine (ACSM, 2017) and the American Stroke Association (Billinger et al., 2014) recommendations for stroke patients. The five weekly 45-minute sessions are divided into (1) three sessions guided and supervised telematically by a physical exercise specialist and a physiotherapist; (2) and two autonomous exercise sessions. The supervised sessions include exercises to work aerobic capacity, muscle strength and endurance, flexibility, agility, and balance. The intensity of these exercises is prescribed individually according to each participant's initial level and are gradually increased as the program progresses. Participants are encouraged to walk at a similar intensity on autonomous physical exercise days as performed in the guided sessions (moderate intensity), based on the Borg scale of perceived exertion (Borg, 1982).
Intervention Type
Behavioral
Intervention Name(s)
Mindfulness-Based Stress Reduction Program
Intervention Description
This intervention follows an adaptation of the scheme and instructions of the official Mindfulness-Based Stress Reduction (MBSR) program designed by Jon Kabat-Zinn. It includes body scanning, sitting meditation, and gentle hatha yoga techniques. An accredited mindfulness instructor leads the 12-week online program, which comprises a presentation session, followed by eight intervention sessions (once a week, lasting 2.5 hours) and an intensive practice session interspersed between sessions six and seven. Apart from the supervised session, the therapist asks participants to carry out some independent practice daily.
Intervention Type
Behavioral
Intervention Name(s)
Computerized Cognitive Training
Intervention Description
An accredited neuropsychologist programs and supervises the computerized cognitive training through the Guttmann Neuropersonal Trainer (GNPT®) platform. The 12-week program consists of five sessions a week (45 minutes each) that include personalized activities planned to stimulate executive functioning, attention, processing speed, and memory.
Primary Outcome Measure Information:
Title
Change in immediate verbal attention after receiving treatment
Description
Forward Digit Span (WAIS III)
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Change in verbal digit working memory after receiving treatment
Description
Backward Digit Span (WAIS III)
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Change in verbal memory after receiving treatment
Description
Rey Auditory Learning Test
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Change in visual memory after receiving treatment
Description
Rey's Complex Figure Test
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Change in executive function, verbal fluency after receiving treatment
Description
Phonetic Fluency is measured using the Controlled Oral Word Association Test, spanish adaptation, and semantic fluency test using the category Animal
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Change in executive function, inhibition after receiving treatment
Description
Stroop Test
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Change in executive function, set-switching task after receiving treatment
Description
Trail Making Test
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Change in language, naming after receiving treatment
Description
Boston naming Test
Time Frame
3 months (at baseline, 3 months from baseline)
Secondary Outcome Measure Information:
Title
Changes in psychological distress
Description
Clinical Outcomes in Routine Evaluation (CORE-OM)
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Changes in depression and anxiety
Description
Depression Anxiety Stress Scale (DASS-21)
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Changes in wellbeing
Description
Ryff Scales of Psychological Wellbeing.
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Changes in Mindfulness
Description
Mindful Attention Awareness Scale (MAAS)
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Changes in White matter integrity
Description
White matter integrity: tractography
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Changes in Resting-state connectivity
Description
Resting state brain activity using fMRI
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Changes in brain volumetry
Description
Grey and white matter volume measured by MRI
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Molecular changes: growth factors (BDNF, SDF1-a, VEGF-A, IGF-1, and NGF), cortisol, protein C reactive, IL-6 and homocysteine levels
Description
Quantification of different biomarkers from blood samples.
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Changes in Microbiota data
Description
Bacterial composition of stool samples in terms of relative abundance
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Changes in Sleep
Description
Pittsburgh Sleep Quality Index (PSQI)
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Changes in Fitness
Description
Senior Fitness Test (SFT)
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Changes in stroke specific quality of life
Description
Stroke-specific Quality of Life Scale (ECVI-38)
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Changes in quality of life
Description
World Health Organization Quality of Life (WHOQOL-BREF)
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Changes in mental fatigue
Description
Fatigue Assessment Scale (FAS)
Time Frame
3 months (at baseline, 3 months from baseline)
Title
Changes in physical activity:
Description
Spanish version of the reduced Minnesota leisure-time physical and activity questionnaire (VREM)
Time Frame
3 months (at baseline, 3 months from baseline)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Individuals aged 18-80 years old Ischemic or hemorrhagic stroke Stroke diagnoses between 3-60 months ago To have consent from a physician to engage in an exercise intervention Fluency in Catalan or Spanish (I.e., able to understand and speak) Accept to take part in the study and sign the informed consent according to the Declaration of Helsinki. Exclusion Criteria: Cognitive impairment (MMSE > 23) Severe aphasia (item 9 of the NIHSS scale ≥ 2) Severe sensory problems Other neurological conditions apart from stroke Severe pre-stroke psychiatric disorders (e.g., bipolar disorder, schizophrenia) History of alcohol or other toxic abuse Exclusion criteria only for MRI examination: Claustrophobia Medical device (e.g., pacemaker implants, stents) Other metal objects in the body
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maria Mataro, PhD
Organizational Affiliation
University of Barcelona
Official's Role
Principal Investigator
Facility Information:
Facility Name
Maria Mataro
City
Barcelona
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
36248000
Citation
Bermudo-Gallaguet A, Ariza M, Dacosta-Aguayo R, Agudelo D, Camins-Vila N, Boldo M, Carrera O, Vidal S, Ferrer-Uris B, Busquets A, Via M, Pera G, Caceres C, Gomis M, Garcia-Molina A, Tormos JM, Arrabe A, Diez G, Dura Mata MJ, Toran-Monserrat P, Soriano-Raya JJ, Domenech S, Perera-Lluna A, Erickson KI, Mataro M. Effects and mechanisms of mindfulness training and physical exercise on cognition, emotional wellbeing, and brain outcomes in chronic stroke patients: Study protocol of the MindFit project randomized controlled trial. Front Aging Neurosci. 2022 Sep 29;14:936077. doi: 10.3389/fnagi.2022.936077. eCollection 2022.
Results Reference
derived

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Exercise the Mind and Brain. A Multimodal Intervention in Stroke

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