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Pilot Study Among Type 2 Diabetes Patients Investigating the Effects of Computerized Cognitive and Physical Activity Programs Combined or Single (DIASCOP) (DIASCOP)

Primary Purpose

Diabetes Mellitus, Type 2

Status
Unknown status
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Physical activity
cognitive training
combined physical and cognitive training
Sponsored by
University Hospital, Clermont-Ferrand
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Diabetes Mellitus, Type 2 focused on measuring Exercise, Physical fitness, Neuropsychological Tests, Cognition, Diabetes Mellitus, Type 2

Eligibility Criteria

50 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Male or female aged between 50 and 70 years old, suffering from type 2 diabetes.

Normal or corrected sight and audition. Being able to engage in physical activity. Being able to give enlightened consent. Being affiliate to social welfare

Exclusion Criteria:

Being unable to meet the study conditions or to answer in French to surveys. Any condition considered, by the investigator, as incompatible with the participation in the study.

Major incapacities. Refusal of participation.

Sites / Locations

  • CHU de Clermont-Ferrand

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Group 1: physical activity then cognitive training

Group 2: Cognitive training then physical activity

Group 3 : resonance frequency breathing then combined physical activity and cognitive training

Arm Description

Using an online-computerized application, physical activities will be prescribed for one month. After a 15 days break, cognitive training activities will be prescribed the same way. A feedback by the patient will be asked fallowing each activity to control the observance.

Contrary to the first group, the second one starts with cognitive training intervention then engages in physical activity in same way as the first group. A feedback by the patient will also be asked fallowing each activity to control the observance

The third group takes part in a 1 month breathing exercise program. After a 15 days break (as the groups 1 and 2), a combined physical activity and cognitive training program is administrated for 1 month. As the others arms, a feedback by the patient will be asked fallowing each activity to control the observance

Outcomes

Primary Outcome Measures

Episodic memory performances
Scores are obtained from delayed memory recall tests from the logical memory subtest of the Wechsler memory scale. It consists of two short narrative stories with an immediate recall phase after each story and a delayed recall phase after 10 minutes. During the delayed recall, each correct detail was awarded with one score point. On a scale of 0 to 50, a higher score means a better detailed recall.
Episodic memory performances
Scores are obtained from delayed memory recall tests from the logical memory subtest of the Wechsler memory scale. It consists of two short narrative stories with an immediate recall phase after each story and a delayed recall phase after 10 minutes. During the delayed recall, each correct detail was awarded with one score point. On a scale of 0 to 50, a higher score means a better detailed recall.
Episodic memory performances
Scores are obtained from delayed memory recall tests from the logical memory subtest of the Wechsler memory scale. It consists of two short narrative stories with an immediate recall phase after each story and a delayed recall phase after 10 minutes. During the delayed recall, each correct detail was awarded with one score point. On a scale of 0 to 50, a higher score means a better detailed recall.

Secondary Outcome Measures

Heart rate variability
Time interval between two heart beats assessed by a monitoring watch (Empatica E4) and belt (Zephyr Bioharness 3)
Heart rate variability
Time interval between two heart beats assessed by a monitoring watch (Empatica E4) and belt (Zephyr Bioharness 3)
Heart rate variability
Time interval between two heart beats assessed by a monitoring watch (Empatica E4) and belt (Zephyr Bioharness 3)
Blood circulation
Assessed by laser speckle contrast imaging (LSCI).
Blood circulation
Assessed by laser speckle contrast imaging (LSCI).
Blood circulation
Assessed by laser speckle contrast imaging (LSCI).
Biomarkers of stress
A salivary sample to test cortisol level and DHEA.
Biomarkers of stress
A salivary sample to test cortisol level and DHEA.
Biomarkers of stress
A salivary sample to test cortisol level and DHEA.
Body Mass index
The ratio between weight and height will be computed to report BMI in kg/m2.
Body Mass index
The ratio between weight and height will be computed to report BMI in kg/m2.
Body Mass index
The ratio between weight and height will be computed to report BMI in kg/m2.
Life satisfaction scale
This scale assesses the feeling of satisfaction of one's life. This scale has 5 items. The minimum score is 5 and the maximum score is 35. A higher score means a higher life satisfaction level.
Life satisfaction scale
This scale assesses the feeling of satisfaction of one's life. This scale has 5 items. The minimum score is 5 and the maximum score is 35. A higher score means a higher life satisfaction level.
Life satisfaction scale
This scale assesses the feeling of satisfaction of one's life. This scale has 5 items. The minimum score is 5 and the maximum score is 35. A higher score means a higher life satisfaction level.
Psychological Outcome Profiles
This survey assesses the patient's satisfaction level before and after the intervention. Five items with a 6-points Likert scale (0 to 5) allow to obtain a score between 0 and 25. A higher score means a better satisfaction level
Psychological Outcome Profiles
This survey assesses the patient's satisfaction level before and after the intervention. Five items with a 6-points Likert scale (0 to 5) allow to obtain a score between 0 and 25. A higher score means a better satisfaction level
Psychological Outcome Profiles
This survey assesses the patient's satisfaction level before and after the intervention. Five items with a 6-points Likert scale (0 to 5) allow to obtain a score between 0 and 25. A higher score means a better satisfaction level
Interoception awareness questionnaire
To assess the awareness of both neutral and negative bodily signals, this scale has 19 items with a 5-points Likert scale (1 to 5). The minimum total score is 9 while the maximum is 95. A higher score means a higher perception of bodily signals.
Interoception awareness questionnaire
To assess the awareness of both neutral and negative bodily signals, this scale has 19 items with a 5-points Likert scale (1 to 5). The minimum total score is 9 while the maximum is 95. A higher score means a higher perception of bodily signals.
Interoception awareness questionnaire
To assess the awareness of both neutral and negative bodily signals, this scale has 19 items with a 5-points Likert scale (1 to 5). The minimum total score is 9 while the maximum is 95. A higher score means a higher perception of bodily signals.
BORB Birmingham Object Recognition Battery
To assess visuospatial processing by asking the participants if two stimuli are orientated the same way.
BORB Birmingham Object Recognition Battery
To assess visuospatial processing by asking the participants if two stimuli are orientated the same way.
BORB Birmingham Object Recognition Battery
To assess visuospatial processing by asking the participants if two stimuli are orientated the same way.
Executive functions
A battery of 5 tests assessing cognitive inhibition (Stroop and Go/No-Go), cognitive flexibility (Trail Making Test), working memory (Nback) and lexical access (verbal fluency) to reflect executive functioning.
Executive functions
A battery of 5 tests assessing cognitive inhibition (Stroop and Go/No-Go), cognitive flexibility (Trail Making Test), working memory (Nback) and lexical access (verbal fluency) to reflect executive functioning.
Executive functions
A battery of 5 tests assessing cognitive inhibition (Stroop and Go/No-Go), cognitive flexibility (Trail Making Test), working memory (Nback) and lexical access (verbal fluency) to reflect executive functioning.
The emotion regulation questionnaire
A questionnaire to measure emotion regulation strategies one favors such as emotion suppression or cognitive reappraisal. This questionnaire has 10 items with a 5-points Likert scale (1 to 5). The score ranges from 5 to 50. A higher score means better emotion regulation strategies.
The emotion regulation questionnaire
A questionnaire to measure emotion regulation strategies one favors such as A questionnaire to measure emotion regulation strategies one favors such as emotion suppression or cognitive reappraisal. This questionnaire has 10 items with a 5-points Likert scale (1 to 5). The score ranges from 5 to 50. A higher score means better emotion regulation strategies.
The emotion regulation questionnaire
A questionnaire to measure emotion regulation strategies one favors such as emotion suppression or cognitive reappraisal. This questionnaire has 10 items with a 5-points Likert scale (1 to 5). The score ranges from 5 to 50. A higher score means better emotion regulation strategies.
Beck Depression Scale
To estimate the level of depression among adults, this scale has 13 items with a 4-points Likert scale (0 to 3). The score ranges from 0 to 39, a higher score means a higher level of depression.
Beck Depression Scale
To estimate the level of depression among adults, this scale has 13 items with a 4-points Likert scale (0 to 3). The score ranges from 0 to 39, a higher score means a higher level of depression.
Beck Depression Scale
To estimate the level of depression among adults, this scale has 13 items with a 4-points Likert scale (0 to 3). The score ranges from 0 to 39, a higher score means a higher level of depression.
Fat/lean mass ratio
The bio-electrical impedance analysis measurements will include total body fat mass (FM in kg), and total body lean mass (LM in kg). Then the fat/lean mass (F/L) ratio will be calculated.
Fat/lean mass ratio
The bio-electrical impedance analysis measurements will include total body fat mass (FM in kg), and total body lean mass (LM in kg). Then the fat/lean mass (F/L) ratio will be calculated.
Fat/lean mass ratio
The bio-electrical impedance analysis measurements will include total body fat mass (FM in kg), and total body lean mass (LM in kg). Then the fat/lean mass (F/L) ratio will be calculated.
Client satisfaction questionnaire
This survey assesses the patient's satisfaction level of the intervention. Eight items with a 4-points Likert scale (1 to 4) allow to obtain a score between 8 and 32. A higher score means a better satisfaction level.
Client satisfaction questionnaire
This survey assesses the patient's satisfaction level of the intervention. Eight items with a 4-points Likert scale (1 to 4) allow to obtain a score between 8 and 32. A higher score means a better satisfaction level.
Client satisfaction questionnaire
This survey assesses the patient's satisfaction level of the intervention. Eight items with a 4-points Likert scale (1 to 4) allow to obtain a score between 8 and 32. A higher score means a better satisfaction level.

Full Information

First Posted
May 21, 2021
Last Updated
May 31, 2021
Sponsor
University Hospital, Clermont-Ferrand
Collaborators
University of Clermont Auvergne (UCA) / LAPSCO
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1. Study Identification

Unique Protocol Identification Number
NCT04915339
Brief Title
Pilot Study Among Type 2 Diabetes Patients Investigating the Effects of Computerized Cognitive and Physical Activity Programs Combined or Single (DIASCOP)
Acronym
DIASCOP
Official Title
Pilot Study Among Type 2 Diabetes Patients Investigating Effects of Computerized Cognitive and Physical Activity Programs Combined or Single.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Unknown status
Study Start Date
June 2021 (Anticipated)
Primary Completion Date
September 2022 (Anticipated)
Study Completion Date
June 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Clermont-Ferrand
Collaborators
University of Clermont Auvergne (UCA) / LAPSCO

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 purpose of this study is to assess the cognitive benefits of combined physical activity and cognitive training on cognitive health compare to physical activity or cognitive training programs singly administrated among type 2 diabetes. Two group in cross over will take part in either physical activity only (for the first one) or cognitive training only (for the second one) for one month then the other way around during the second month. A fallow up will be administrated 3 months later.
Detailed Description
The growing Type 2 diabetes prevalence is associated with health, economic and social consequences. As such, type 2 diabetes is recognized as major health issue. Health care should go on after being discharged from the hospital in order to promote cognitive autonomy. Physical activity and cognitive training are two interventions often recommended individually to benefit cognition among type 2 diabetes patients. Yet, a program combining physical activity and cognitive training might be more effective to favor cognitive health. In this study, diabetes patient between 50 and 75 years old will be allocated randomly in 3 intervention groups in order to have a homogeneous distribution of the education level, sex and age across the 3 samples. The first group will take part in a physical activity program the first month and in a cognitive training one the second. The second group will be cross-over meaning taking part in a cognitive training program the first month and engaging in the physical activity one the second month. The last group will engage in a program based on resonance frequency breathing the first month (as a control condition), then in a combined physical activity and cognitive training program. Between the 2 interventions, there will be a 15 days break (limiting the transfer of the effect of one intervention onto another). At the beginning of the study, a screening will allow to identify possible exclusion criteria (health factors that could influence the main outcomes). At the beginning (baseline) of the first intervention and after each month, neuropsychological tests assessing cognitive and psychological health as well as well-being. Physiological parameters such as heart rate variability, cortisol and DHEA levels, muscle and lean mass, blood circulation (assessed by Laser speckle contrast imaging). A whole session (psychological and physiological testing) should take 1 h 30. Besides, participants will complete online questionnaires. They have one week after the testing to complete those surveys. If they are late an email will be sent before a phone call in the case the delay goes on. The main outcome is the increase of the cognitive variables after the intervention. It is expected that the physical activity and cognitive training combined program will benefit cognitive functioning more than either of those programs administrated individually. To investigate to long-term effects of the intervention, a fallow up 3 months later will be conduct

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2
Keywords
Exercise, Physical fitness, Neuropsychological Tests, Cognition, Diabetes Mellitus, Type 2

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Group 1: physical activity (one month) then cognitive training (one month) Group 2: Cognitive training (one month) then physical activity (one month) Group 3 : resonance frequency breathing (one month) then combined physical activity and cognitive (one month) training
Masking
ParticipantInvestigatorOutcomes Assessor
Masking Description
The study hypothesis is not given to the participants and the investigator will not be aware of the group the participants have been allocated to.
Allocation
Randomized
Enrollment
81 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group 1: physical activity then cognitive training
Arm Type
Experimental
Arm Description
Using an online-computerized application, physical activities will be prescribed for one month. After a 15 days break, cognitive training activities will be prescribed the same way. A feedback by the patient will be asked fallowing each activity to control the observance.
Arm Title
Group 2: Cognitive training then physical activity
Arm Type
Experimental
Arm Description
Contrary to the first group, the second one starts with cognitive training intervention then engages in physical activity in same way as the first group. A feedback by the patient will also be asked fallowing each activity to control the observance
Arm Title
Group 3 : resonance frequency breathing then combined physical activity and cognitive training
Arm Type
Experimental
Arm Description
The third group takes part in a 1 month breathing exercise program. After a 15 days break (as the groups 1 and 2), a combined physical activity and cognitive training program is administrated for 1 month. As the others arms, a feedback by the patient will be asked fallowing each activity to control the observance
Intervention Type
Behavioral
Intervention Name(s)
Physical activity
Intervention Description
The intervention is administrated through a computerized application as prescribed exercises (cognitive or physical). The specific measures that will be used to determine the effect of the intervention are psychological variables (mood, anxiety, well-being, cognitive variables…) and physical ones (Heart rate variability, stress biomarkers, fat and muscle mass, blood circulation…).
Intervention Type
Behavioral
Intervention Name(s)
cognitive training
Intervention Description
The intervention is administrated through a computerized application as prescribed exercises (cognitive or physical). The specific measures that will be used to determine the effect of the intervention are psychological variables (mood, anxiety, well-being, cognitive variables…) and physical ones (Heart rate variability, stress biomarkers, fat and muscle mass, blood circulation…).
Intervention Type
Behavioral
Intervention Name(s)
combined physical and cognitive training
Intervention Description
The intervention is administrated through a computerized application as prescribed exercises (cognitive or physical). The specific measures that will be used to determine the effect of the intervention are psychological variables (mood, anxiety, well-being, cognitive variables…) and physical ones (Heart rate variability, stress biomarkers, fat and muscle mass, blood circulation…).
Primary Outcome Measure Information:
Title
Episodic memory performances
Description
Scores are obtained from delayed memory recall tests from the logical memory subtest of the Wechsler memory scale. It consists of two short narrative stories with an immediate recall phase after each story and a delayed recall phase after 10 minutes. During the delayed recall, each correct detail was awarded with one score point. On a scale of 0 to 50, a higher score means a better detailed recall.
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
Episodic memory performances
Description
Scores are obtained from delayed memory recall tests from the logical memory subtest of the Wechsler memory scale. It consists of two short narrative stories with an immediate recall phase after each story and a delayed recall phase after 10 minutes. During the delayed recall, each correct detail was awarded with one score point. On a scale of 0 to 50, a higher score means a better detailed recall.
Time Frame
Month 2 (a week after the second intervention)
Title
Episodic memory performances
Description
Scores are obtained from delayed memory recall tests from the logical memory subtest of the Wechsler memory scale. It consists of two short narrative stories with an immediate recall phase after each story and a delayed recall phase after 10 minutes. During the delayed recall, each correct detail was awarded with one score point. On a scale of 0 to 50, a higher score means a better detailed recall.
Time Frame
Month 3
Secondary Outcome Measure Information:
Title
Heart rate variability
Description
Time interval between two heart beats assessed by a monitoring watch (Empatica E4) and belt (Zephyr Bioharness 3)
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
Heart rate variability
Description
Time interval between two heart beats assessed by a monitoring watch (Empatica E4) and belt (Zephyr Bioharness 3)
Time Frame
Month 2 (a week after the second intervention)
Title
Heart rate variability
Description
Time interval between two heart beats assessed by a monitoring watch (Empatica E4) and belt (Zephyr Bioharness 3)
Time Frame
Month 3
Title
Blood circulation
Description
Assessed by laser speckle contrast imaging (LSCI).
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
Blood circulation
Description
Assessed by laser speckle contrast imaging (LSCI).
Time Frame
Month 2 (a week after the second intervention)
Title
Blood circulation
Description
Assessed by laser speckle contrast imaging (LSCI).
Time Frame
Month 3
Title
Biomarkers of stress
Description
A salivary sample to test cortisol level and DHEA.
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
Biomarkers of stress
Description
A salivary sample to test cortisol level and DHEA.
Time Frame
Month 2 (a week after the second intervention)
Title
Biomarkers of stress
Description
A salivary sample to test cortisol level and DHEA.
Time Frame
Month 3
Title
Body Mass index
Description
The ratio between weight and height will be computed to report BMI in kg/m2.
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
Body Mass index
Description
The ratio between weight and height will be computed to report BMI in kg/m2.
Time Frame
Month 2 (a week after the second intervention)
Title
Body Mass index
Description
The ratio between weight and height will be computed to report BMI in kg/m2.
Time Frame
Month 3
Title
Life satisfaction scale
Description
This scale assesses the feeling of satisfaction of one's life. This scale has 5 items. The minimum score is 5 and the maximum score is 35. A higher score means a higher life satisfaction level.
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
Life satisfaction scale
Description
This scale assesses the feeling of satisfaction of one's life. This scale has 5 items. The minimum score is 5 and the maximum score is 35. A higher score means a higher life satisfaction level.
Time Frame
Month 2 (a week after the second intervention)
Title
Life satisfaction scale
Description
This scale assesses the feeling of satisfaction of one's life. This scale has 5 items. The minimum score is 5 and the maximum score is 35. A higher score means a higher life satisfaction level.
Time Frame
Month 3
Title
Psychological Outcome Profiles
Description
This survey assesses the patient's satisfaction level before and after the intervention. Five items with a 6-points Likert scale (0 to 5) allow to obtain a score between 0 and 25. A higher score means a better satisfaction level
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
Psychological Outcome Profiles
Description
This survey assesses the patient's satisfaction level before and after the intervention. Five items with a 6-points Likert scale (0 to 5) allow to obtain a score between 0 and 25. A higher score means a better satisfaction level
Time Frame
Month 2 (a week after the second intervention)
Title
Psychological Outcome Profiles
Description
This survey assesses the patient's satisfaction level before and after the intervention. Five items with a 6-points Likert scale (0 to 5) allow to obtain a score between 0 and 25. A higher score means a better satisfaction level
Time Frame
Month 3
Title
Interoception awareness questionnaire
Description
To assess the awareness of both neutral and negative bodily signals, this scale has 19 items with a 5-points Likert scale (1 to 5). The minimum total score is 9 while the maximum is 95. A higher score means a higher perception of bodily signals.
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
Interoception awareness questionnaire
Description
To assess the awareness of both neutral and negative bodily signals, this scale has 19 items with a 5-points Likert scale (1 to 5). The minimum total score is 9 while the maximum is 95. A higher score means a higher perception of bodily signals.
Time Frame
Month 2 (a week after the second intervention)
Title
Interoception awareness questionnaire
Description
To assess the awareness of both neutral and negative bodily signals, this scale has 19 items with a 5-points Likert scale (1 to 5). The minimum total score is 9 while the maximum is 95. A higher score means a higher perception of bodily signals.
Time Frame
Month 3
Title
BORB Birmingham Object Recognition Battery
Description
To assess visuospatial processing by asking the participants if two stimuli are orientated the same way.
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
BORB Birmingham Object Recognition Battery
Description
To assess visuospatial processing by asking the participants if two stimuli are orientated the same way.
Time Frame
Month 2 (a week after the second intervention)
Title
BORB Birmingham Object Recognition Battery
Description
To assess visuospatial processing by asking the participants if two stimuli are orientated the same way.
Time Frame
Month 3
Title
Executive functions
Description
A battery of 5 tests assessing cognitive inhibition (Stroop and Go/No-Go), cognitive flexibility (Trail Making Test), working memory (Nback) and lexical access (verbal fluency) to reflect executive functioning.
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
Executive functions
Description
A battery of 5 tests assessing cognitive inhibition (Stroop and Go/No-Go), cognitive flexibility (Trail Making Test), working memory (Nback) and lexical access (verbal fluency) to reflect executive functioning.
Time Frame
Month 2 (a week after the second intervention)
Title
Executive functions
Description
A battery of 5 tests assessing cognitive inhibition (Stroop and Go/No-Go), cognitive flexibility (Trail Making Test), working memory (Nback) and lexical access (verbal fluency) to reflect executive functioning.
Time Frame
Month 3
Title
The emotion regulation questionnaire
Description
A questionnaire to measure emotion regulation strategies one favors such as emotion suppression or cognitive reappraisal. This questionnaire has 10 items with a 5-points Likert scale (1 to 5). The score ranges from 5 to 50. A higher score means better emotion regulation strategies.
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
The emotion regulation questionnaire
Description
A questionnaire to measure emotion regulation strategies one favors such as A questionnaire to measure emotion regulation strategies one favors such as emotion suppression or cognitive reappraisal. This questionnaire has 10 items with a 5-points Likert scale (1 to 5). The score ranges from 5 to 50. A higher score means better emotion regulation strategies.
Time Frame
Month 2 (a week after the second intervention)
Title
The emotion regulation questionnaire
Description
A questionnaire to measure emotion regulation strategies one favors such as emotion suppression or cognitive reappraisal. This questionnaire has 10 items with a 5-points Likert scale (1 to 5). The score ranges from 5 to 50. A higher score means better emotion regulation strategies.
Time Frame
Month 3
Title
Beck Depression Scale
Description
To estimate the level of depression among adults, this scale has 13 items with a 4-points Likert scale (0 to 3). The score ranges from 0 to 39, a higher score means a higher level of depression.
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
Beck Depression Scale
Description
To estimate the level of depression among adults, this scale has 13 items with a 4-points Likert scale (0 to 3). The score ranges from 0 to 39, a higher score means a higher level of depression.
Time Frame
Month 2 (a week after the second intervention)
Title
Beck Depression Scale
Description
To estimate the level of depression among adults, this scale has 13 items with a 4-points Likert scale (0 to 3). The score ranges from 0 to 39, a higher score means a higher level of depression.
Time Frame
Month 3
Title
Fat/lean mass ratio
Description
The bio-electrical impedance analysis measurements will include total body fat mass (FM in kg), and total body lean mass (LM in kg). Then the fat/lean mass (F/L) ratio will be calculated.
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
Fat/lean mass ratio
Description
The bio-electrical impedance analysis measurements will include total body fat mass (FM in kg), and total body lean mass (LM in kg). Then the fat/lean mass (F/L) ratio will be calculated.
Time Frame
Month 2 (a week after the second intervention)
Title
Fat/lean mass ratio
Description
The bio-electrical impedance analysis measurements will include total body fat mass (FM in kg), and total body lean mass (LM in kg). Then the fat/lean mass (F/L) ratio will be calculated.
Time Frame
Month 3
Title
Client satisfaction questionnaire
Description
This survey assesses the patient's satisfaction level of the intervention. Eight items with a 4-points Likert scale (1 to 4) allow to obtain a score between 8 and 32. A higher score means a better satisfaction level.
Time Frame
Month 1 (Between 1 day and a week before and after the first intervention)
Title
Client satisfaction questionnaire
Description
This survey assesses the patient's satisfaction level of the intervention. Eight items with a 4-points Likert scale (1 to 4) allow to obtain a score between 8 and 32. A higher score means a better satisfaction level.
Time Frame
Month 2 (a week after the second intervention)
Title
Client satisfaction questionnaire
Description
This survey assesses the patient's satisfaction level of the intervention. Eight items with a 4-points Likert scale (1 to 4) allow to obtain a score between 8 and 32. A higher score means a better satisfaction level.
Time Frame
Month 3

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female aged between 50 and 70 years old, suffering from type 2 diabetes. Normal or corrected sight and audition. Being able to engage in physical activity. Being able to give enlightened consent. Being affiliate to social welfare Exclusion Criteria: Being unable to meet the study conditions or to answer in French to surveys. Any condition considered, by the investigator, as incompatible with the participation in the study. Major incapacities. Refusal of participation.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Lise LACLAUTRE
Phone
+33473754963
Email
promo_interne_drci@chu-clermontferrand.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
FrΓ©dΓ©ric Dutheil
Organizational Affiliation
University Hospital, Clermont-Ferrand
Official's Role
Principal Investigator
Facility Information:
Facility Name
CHU de Clermont-Ferrand
City
Clermont-Ferrand
ZIP/Postal Code
63000
Country
France
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lise Laclautre
Phone
+33473754963
Email
promo_interne_drci@chu-clermontferrand.fr
First Name & Middle Initial & Last Name & Degree
FrΓ©dΓ©ric Dutheil

12. IPD Sharing Statement

Citations:
PubMed Identifier
35777867
Citation
Magnon V, Dutheil F, Tauveron I, Mille J, Baker JS, Brusseau V, Silvert L, Izaute M, Vallet GT. Does an increase in physiological indexes predict better cognitive performance: the PhyCog randomised cross-over protocol in type 2 diabetes. BMJ Open. 2022 Jul 1;12(7):e060057. doi: 10.1136/bmjopen-2021-060057.
Results Reference
derived

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Pilot Study Among Type 2 Diabetes Patients Investigating the Effects of Computerized Cognitive and Physical Activity Programs Combined or Single (DIASCOP)

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