search
Back to results

Dual-task Training Effects on Cognition in Breast Cancer Survivors: the BRAINonFIT Study (BRAINonFIT). (BRAINonFIT)

Primary Purpose

Breast Cancer Survivors, Cognitive Impairment, Executive Dysfunction

Status
Not yet recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Exercise
Dual-Task Training
Health and Wellness
Sponsored by
University of Seville
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Breast Cancer Survivors focused on measuring Cancer-related Cognitive Impairment, Physical exercise, dual motor-cognitive tasks, cognitive stimulation, Neurocognitive disorders

Eligibility Criteria

25 Years - 65 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Diagnosed with stage I-IIIA breast cancer Completed primary treatment, including surgery, radiotherapy and/or chemotherapy Scheduled to receive adjuvant endocrine therapy, or currently receiving adjuvant endocrine therapy Without functional limitations or other illnesses that condition and prevent them from practising intense physical exercise FACT-Cog questionnaire score ≥ 10th percentile considering age groups Fluency in Spanish (spoken and written) Exclusion Criteria: Undergoing radiotherapy and/or chemotherapy FACT-Cog questionnaire score ≤ 10th percentile considering age groups Congenital heart disease Chronic lung disease Severe psychiatric disorders History of substance abuse, or dependence (other than tobacco) Mood disorders require treatment (anxiety or depression) Relapses (2-3 months before the study start)

Sites / Locations

  • SADUS - Servicio de Actividades Deportivas de la Universidad de Sevilla
  • Laboratorio de Ciencias del Deporte
  • Oncoavanze

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Active Comparator

Arm Label

Exercise Intervention

Dual Motor-Cognitive Intervention

Health and Wellness Intervention

Arm Description

This arm will receive a 5-month (20 weeks) supervised exercise program based on aerobic and resistance/strength training together with a weekly calorie or step challenge.

This arm will receive a 5-month (20 weeks) supervised and simultaneous dual-task program based on aerobic, resistance, and cognitive stimulation training together with a weekly calorie or step challenge

This arm will receive a 5-month health and wellness program.

Outcomes

Primary Outcome Measures

Executive Function (Cognitive Flexibility and Processing Speed)
Trail Making Test A and B (minimum and maximum values, defined by the time in seconds, depend on the age- and education-normalised groups; higher scores mean worse results)

Secondary Outcome Measures

Inhibitory Control and Concentration
Stroop Color and Word test (minimum and maximum values, defined by the time in seconds, depend on the age- and education-normalised groups; higher scores mean worse results)
Verbal Intelligence, Non-verbal Intelligence, Verbal memory, and Non-verbal Memory
Reynolds Intellectual Assessment Scale (Global index values range from ≤ 69 to ≥ 130, mean value of 100; higher scores mean better results)
Learning Ability
Wechsler Memory Scale subtest "word pairs" (The subtest score range from 40 to 60, mean value of 100; higher scores mean better results)
Perceived Cognitive Functions
Functional Assessment of Cancer Therapy: Cognition (FACT-Cog) (Total score ranges from 0 to 148; higher scores mean better results)
Max. Oxygen Consumption
Modified Bruce Test (80% sub-max)
Muscular Strength of shoulder and knee extensors
Isokinetic dynamometer
Range of Movement
Manual Goniometer
Forced Vital Capacity (FVC) and Forced Expiratory Volume (FEV)
Spirometry (FEV/FVC ratio, represented in percentages)
Volume of physical activity
Accelerometer (Volume in minutes per week)
Intensity of Physical Activity
Accelerometer (Intensity in metabolic equivalents)
Weight and Height
Body Mass Index (weight and height will be combined to report BMI in kg/m^2)
Brain-Derived Neurotrophic Factor (BDNF), Vascular Endothelial Growth Factor (VEGF), Fibroblast Growth Factor 17 (FDF-17), Soluble Klotho (S-KL)
Concentration of these proteins in plasma by ELISA kit (Concentration of these proteins will be expressed in pg/mL or ng/mL)
Fatigue
Functional Assessment of Chronic Illness Therapy: Fatigue (FACIT-F) (Total score range from 0 to 52; higher scores mean better results)
Pain Scale
Visual Analogue Scale (Total score ranges from 0 to 10; higher scores mean worse results)
Depression
Back Depression Inventory (Total score ranges from 0 to 63; higher scores mean worse results)
Anxiety
State-Trait Anxiety Inventory (The score ranges from 20 to 80; higher scores mean worse results)

Full Information

First Posted
September 22, 2023
Last Updated
October 2, 2023
Sponsor
University of Seville
search

1. Study Identification

Unique Protocol Identification Number
NCT06073717
Brief Title
Dual-task Training Effects on Cognition in Breast Cancer Survivors: the BRAINonFIT Study (BRAINonFIT).
Acronym
BRAINonFIT
Official Title
Dual-task Training Effects on Cancer-related Cognitive Impairment and Muscle-brain Crosstalk Biomarkers in Breast Cancer Survivors: the BRAINonFIT Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 2023 (Anticipated)
Primary Completion Date
August 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Seville

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 goal of this interventional study is to assess the effects of either physical exercise program or combined with cognitive training (dual motor and cognitive training program) on breast cancer survivors. The main questions it aims to answer are: Analyze the effectiveness of a supervised dual-task training program or a physical exercise program on the executive functions of the participants. Evaluate the impact of both interventions on physical function, emotional aspects, and important biomarkers related to muscle-brain crosstalk. Participants will perform a 20-week supervised and controlled program, three times a week, along with weekly calorie and step challenges. Researchers will compare the dual-task training group, with the physical exercise group, and with a control group, which will perform the guideline recommendations of physical activity (non-supervised) to see how these intervention approaches can impact cognitive functions, physical functions, emotional aspects, and biomarkers related to muscle-brain crosstalk. Assessments will take place at three-time points: at baseline, after the intervention (20 weeks post-baseline) and after a 12-week follow-up period (32 weeks post-baseline).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer Survivors, Cognitive Impairment, Executive Dysfunction
Keywords
Cancer-related Cognitive Impairment, Physical exercise, dual motor-cognitive tasks, cognitive stimulation, Neurocognitive disorders

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This study has been designed as a randomised, controlled, longitudinal (20 weeks), three-arm, parallel study with a follow-up phase (12 weeks).
Masking
Participant
Masking Description
Regarding the control of experimental bias, simple blinding will be used. Thus, participants will be blinded to the research problem. They will be informed that three interventions will be applied (without comment on specific details of each one) randomly allocated, to compare the impact on cognitive functions, circulating levels of certain biomarkers, and different symptoms associated with breast cancer. Therefore, study participants will not be able to know to which experimental or control group they belong.
Allocation
Randomized
Enrollment
108 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Exercise Intervention
Arm Type
Experimental
Arm Description
This arm will receive a 5-month (20 weeks) supervised exercise program based on aerobic and resistance/strength training together with a weekly calorie or step challenge.
Arm Title
Dual Motor-Cognitive Intervention
Arm Type
Experimental
Arm Description
This arm will receive a 5-month (20 weeks) supervised and simultaneous dual-task program based on aerobic, resistance, and cognitive stimulation training together with a weekly calorie or step challenge
Arm Title
Health and Wellness Intervention
Arm Type
Active Comparator
Arm Description
This arm will receive a 5-month health and wellness program.
Intervention Type
Behavioral
Intervention Name(s)
Exercise
Intervention Description
Participants will complete a 5-month exercise program structured in 4 blocks of 5 weeks. Three supervised and combined aerobic/strength exercise sessions each week will be performed together with an aerobic weekly challenge. Aerobic exercise will be performed for 20-30 minutes using a treadmill, bicycle, or circuit training at light to moderate intensities (40-75% of heart rate reserve) during the first two blocks; gradually achieving high intensity (>75% of HHR) in the last two blocks. Heart rate and the subjective perception of the exertion scale (6-20 Borg scale) will be monitored. Strength exercises will be started at light to moderate intensities (2 sets of 15-20 repetitions at 40-50% of repetition maximum), performed muscle actions at high intensities in the last two blocks (2 sets of 8-15 repetitions at 50-75% RM); using elastic bands, free weights, and weights gym exercises.
Intervention Type
Behavioral
Intervention Name(s)
Dual-Task Training
Intervention Description
Participants will complete the same four-block exercise program in terms of type, frequency, intensity, and volume of physical/motor training. Simultaneous with the progression of physical/motor training, the complexity of cognitive stimulation will be increased according to the performance of the participants. General dual-task training will be performed, which describes the use of a physical/motor intervention with different cognitive stimulations (memory, language, intelligence, attention, processing speed, calculation, inhibitory control) that are not specific to the methods to be used for their assessment.
Intervention Type
Behavioral
Intervention Name(s)
Health and Wellness
Intervention Description
Participants randomly assigned to the health and wellness group will be advised and re-educated to support and improve health aspects. Participants in this group will aim to achieve the physical activity recommendations, and in addition, they will receive bi-weekly emails and phone call coaching with tools to empower patients with knowledge about physical exercise, nutrition, and brain health guidelines. Following completion of the 5-month exercise program, this group will receive an exercise program for 12 weeks.
Primary Outcome Measure Information:
Title
Executive Function (Cognitive Flexibility and Processing Speed)
Description
Trail Making Test A and B (minimum and maximum values, defined by the time in seconds, depend on the age- and education-normalised groups; higher scores mean worse results)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Secondary Outcome Measure Information:
Title
Inhibitory Control and Concentration
Description
Stroop Color and Word test (minimum and maximum values, defined by the time in seconds, depend on the age- and education-normalised groups; higher scores mean worse results)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Verbal Intelligence, Non-verbal Intelligence, Verbal memory, and Non-verbal Memory
Description
Reynolds Intellectual Assessment Scale (Global index values range from ≤ 69 to ≥ 130, mean value of 100; higher scores mean better results)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Learning Ability
Description
Wechsler Memory Scale subtest "word pairs" (The subtest score range from 40 to 60, mean value of 100; higher scores mean better results)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Perceived Cognitive Functions
Description
Functional Assessment of Cancer Therapy: Cognition (FACT-Cog) (Total score ranges from 0 to 148; higher scores mean better results)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Max. Oxygen Consumption
Description
Modified Bruce Test (80% sub-max)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Muscular Strength of shoulder and knee extensors
Description
Isokinetic dynamometer
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Range of Movement
Description
Manual Goniometer
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Forced Vital Capacity (FVC) and Forced Expiratory Volume (FEV)
Description
Spirometry (FEV/FVC ratio, represented in percentages)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Volume of physical activity
Description
Accelerometer (Volume in minutes per week)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Intensity of Physical Activity
Description
Accelerometer (Intensity in metabolic equivalents)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Weight and Height
Description
Body Mass Index (weight and height will be combined to report BMI in kg/m^2)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Brain-Derived Neurotrophic Factor (BDNF), Vascular Endothelial Growth Factor (VEGF), Fibroblast Growth Factor 17 (FDF-17), Soluble Klotho (S-KL)
Description
Concentration of these proteins in plasma by ELISA kit (Concentration of these proteins will be expressed in pg/mL or ng/mL)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Fatigue
Description
Functional Assessment of Chronic Illness Therapy: Fatigue (FACIT-F) (Total score range from 0 to 52; higher scores mean better results)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Pain Scale
Description
Visual Analogue Scale (Total score ranges from 0 to 10; higher scores mean worse results)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Depression
Description
Back Depression Inventory (Total score ranges from 0 to 63; higher scores mean worse results)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)
Title
Anxiety
Description
State-Trait Anxiety Inventory (The score ranges from 20 to 80; higher scores mean worse results)
Time Frame
Baseline (week 0); Post-intervention (25 weeks post-baseline); and Post-follow up (32 weeks post-baseline)

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
25 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Diagnosed with stage I-IIIA breast cancer Completed primary treatment, including surgery, radiotherapy and/or chemotherapy Scheduled to receive adjuvant endocrine therapy, or currently receiving adjuvant endocrine therapy Without functional limitations or other illnesses that condition and prevent them from practising intense physical exercise FACT-Cog questionnaire score ≥ 10th percentile considering age groups Fluency in Spanish (spoken and written) Exclusion Criteria: Undergoing radiotherapy and/or chemotherapy FACT-Cog questionnaire score ≤ 10th percentile considering age groups Congenital heart disease Chronic lung disease Severe psychiatric disorders History of substance abuse, or dependence (other than tobacco) Mood disorders require treatment (anxiety or depression) Relapses (2-3 months before the study start)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jesus Orellana
Phone
691436904
Email
orellanajaenjesus1995@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Luis Carrasco Páez, PhD
Phone
629084764
Email
lcarrasco@us.es
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matilde Mora Fernández, PhD
Organizational Affiliation
University of Seville
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Luis Carrasco Páez, PhD
Organizational Affiliation
University of Seville
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Jesús Orellana Jaén
Organizational Affiliation
University of Seville
Official's Role
Principal Investigator
Facility Information:
Facility Name
SADUS - Servicio de Actividades Deportivas de la Universidad de Sevilla
City
Sevilla
ZIP/Postal Code
41012
Country
Spain
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jorge Tihriet
Phone
95.448.77.00
Email
sadus@us.es
Facility Name
Laboratorio de Ciencias del Deporte
City
Sevilla
ZIP/Postal Code
41013
Country
Spain
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Alfonso J García González
Phone
95.455.17.00
Email
fce-informacion@us.es
Facility Name
Oncoavanze
City
Sevilla
ZIP/Postal Code
41013
Country
Spain
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lourdes Valero
Phone
954 231 459
Email
info@oncoavanze.es

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
37480454
Citation
Jesus OJ, Luis CP, Matilde MF. Effects of exercise on cancer-related cognitive impairment in breast cancer survivors: a scoping review. Breast Cancer. 2023 Nov;30(6):885-909. doi: 10.1007/s12282-023-01484-z. Epub 2023 Jul 22.
Results Reference
background

Learn more about this trial

Dual-task Training Effects on Cognition in Breast Cancer Survivors: the BRAINonFIT Study (BRAINonFIT).

We'll reach out to this number within 24 hrs