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Exercise, Hypoxia and CPC in TBI Patients (TCECAM)

Primary Purpose

Traumatic Brain Injury

Status
Completed
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
cognitive activities
Exercise program
Muscle electro-stimulation
Intermittent hypobaric hypoxia
Sponsored by
University of Barcelona
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Traumatic Brain Injury focused on measuring Traumatic brain injury, Exercise, Psychology, Physiology, Progenitor cells, Hypoxia

Eligibility Criteria

20 Years - 60 Years (Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients who suffered severe TBI more than one year previously with physical or psychological sequelae.
  • Written informed consent from patient

Exclusion Criteria:

  • Epilepsy
  • Any medical or psychological contraindications for implementing the program of physical activity or hypobaric chamber.
  • Inclusion in other ongoing study
  • Refuse consent

Sites / Locations

  • University of Barcelona

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Placebo Comparator

Active Comparator

Active Comparator

Arm Label

Control group

Exercise group

Muscle electro-stimulation and IHH

Arm Description

Once a week there will be an attendance cognitive session (specific sessions designed to work on aspects related to body perception, movement, space) and the extraction of blood samples will be carried out to determine the progenitor cells on the same day of the active groups.

Patients with past history of TBI will perform exercise sessions two hours three days a week during 12 weeks. The sessions will consist of aerobic, strength, flexibility, proprioception and balance activities and muscle electro-stimulation sessions or cycling sessions.

Patients with past history of TBI will perform a 12 weeks program: intermittent hypobaric hypoxia (IHH) 2 hours at a simulated altitude of 4500 meters 3 days/week. Muscle electro-stimulation for two periods of 20 minutes during the stay in the hypobaric chamber.

Outcomes

Primary Outcome Measures

Change from initial physical stress test at one week post-intervention
Physical graded maximum stress tests are performed on a cycle ergometer controlling the workload, in order to evaluate physical capacity and adaptation to different intensities of effort.While performance of these tests are conducted, cardiocirculatory (control of heart rate, blood pressure measurement, continuous ECG) and respiratory (breathing gases analysis) are monitored to observe the adaptation to the effort.
Change from initial psychological test at one weeks after intervention
Psychological tests evaluated features of language and work (verbal memory-RAVLT), Trail Making Test (TMT A and B), Stroop Test, working memory capacity and attention (WAIS III), information processing speed (WAIS III), orientation and verbal fluency (Barcelona test), executive functions (WAIS III and Tower of London tests) and estimated premorbid intelligence index (vocabulary, WAIS III). Reduced Paced Auditory Serial Addition Test (PASAT-G)

Secondary Outcome Measures

Circulating progenitor cells increase
Blood CD34 staining and flow cytometry assay in accordance with ISHAGE guidelines (Keeney et al., 1998). CD34 cells/µL.

Full Information

First Posted
March 1, 2014
Last Updated
March 7, 2014
Sponsor
University of Barcelona
Collaborators
Ministerio de Economía y Competitividad, Spain
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1. Study Identification

Unique Protocol Identification Number
NCT02083445
Brief Title
Exercise, Hypoxia and CPC in TBI Patients
Acronym
TCECAM
Official Title
Exercise, Muscle Electro-stimulation and Intermittent Hypobaric Hypoxia Program and Circulating Progenitor Cells in Traumatic Brain Injured Patients
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Completed
Study Start Date
November 2011 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
February 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Barcelona
Collaborators
Ministerio de Economía y Competitividad, Spain

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Circulating progenitor cells (CPC) treatments may have great potential for the recovery of neurons and brain function. Our group has reported how exposure to intermittent hypobaric hypoxia with superficial muscle electrostimulation is able to increase the concentration of CPC in peripheral blood in humans. Therefore, we believe that through physical activities and exposure to intermittent hypobaric hypoxia for a period, it will increase CPC in the blood of subjects who have suffered a severe Traumatic Brain Injury (TBI) one or more years ago, promoting regeneration and functional and cognitive recovery. The study primary end-point is to improve physical or psychological functioning of participants with TBI with a program of exercise, muscle electro-stimulation (ME) and/or intermittent-hypobaric-hypoxia (IHH). Secondary end-points are to increase and maintain CPC and also to study their possible relationship with physical or psychological improvement of participants with Traumatic Brain Injury (TBI). In order to achieve these objectives investigators have designed a randomized controlled trial that will include those patients who suffered severe TBI more than one year previously with physical or psychological sequelae. Exercise, muscle electro-stimulation (ME) and/or intermittent hypobaric hypoxia (IHH) programs will be applied during twelve weeks. Psychological and physical stress tests will carry out before and after the program and CPC will measure at the beginning, every two weeks, and at the end of the program.
Detailed Description
Clinical, experimental, case control and prospective study. Inclusion criteria are: patients who suffered severe TBI more than one year previously with physical or psychological sequelae, male sex, and age 20-60 years old. Patients with epilepsy are not included. The study was approved by the institution's Research Ethics Committee and informed consent was obtained from the patients. A program of three days per week during twelve weeks will be applied to the active groups: one, exercise and muscle electrical stimulation, and the other, exercise, muscle electrical stimulation and IHH chamber exposure. Control group participants will follow a a day of cognitive activities one day per week during 12 weeks. Psychological and physical stress tests are carried out before and after the program. Psychological tests evaluate features of language and work (verbal memory-RAVLT), Trail Making Test (TMT A and B), Stroop Test, working memory capacity and attention (WAIS III), information processing speed (WAIS III), orientation and verbal fluency (Barcelona test), executive functions (WAIS III and Tower of London tests) and estimated premorbid intelligence index (vocabulary, WAIS III). Reduced Paced Auditory Serial Addition Test (PASAT-G) evaluate work memory components. Physical graded maximum stress tests were performed on a cycle ergometer increasing progressively the workload, in order to evaluate physical capacity and adaptation to different intensities of effort. CPC (CD34+) are measured in peripheral blood according to a previously used method (Viscor et al., 2009), at the beginning, every two weeks, and at the end of the program (blood samples were always obtained before the exercise sessions). Statistical analysis: data will express as mean, median, standard deviation and interquartile range as appropriate. The continuous variables will compare using the Mann-Whitney U test. Wilcoxon signed rank test and Friedman test are used for repeated measures. All tests will perform using Statistical Package for the Social Sciences (SPSS) v.13. Statistical significance was set at P<0.05.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Traumatic Brain Injury
Keywords
Traumatic brain injury, Exercise, Psychology, Physiology, Progenitor cells, Hypoxia

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
21 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
Once a week there will be an attendance cognitive session (specific sessions designed to work on aspects related to body perception, movement, space) and the extraction of blood samples will be carried out to determine the progenitor cells on the same day of the active groups.
Arm Title
Exercise group
Arm Type
Active Comparator
Arm Description
Patients with past history of TBI will perform exercise sessions two hours three days a week during 12 weeks. The sessions will consist of aerobic, strength, flexibility, proprioception and balance activities and muscle electro-stimulation sessions or cycling sessions.
Arm Title
Muscle electro-stimulation and IHH
Arm Type
Active Comparator
Arm Description
Patients with past history of TBI will perform a 12 weeks program: intermittent hypobaric hypoxia (IHH) 2 hours at a simulated altitude of 4500 meters 3 days/week. Muscle electro-stimulation for two periods of 20 minutes during the stay in the hypobaric chamber.
Intervention Type
Other
Intervention Name(s)
cognitive activities
Intervention Description
Participants followed a day of cognitive activities 1 day (1 hour/day) per week during 12 weeks.
Intervention Type
Other
Intervention Name(s)
Exercise program
Intervention Description
Exercise program of endurance, resistance and proprioception exercises, comprising three sessions per week and muscle electro-stimulation was applied using the Compex Vitality® vascular and capillarization program with electrodes fixed in quadriceps and abdominal muscles or cycling exercise.
Intervention Type
Device
Intervention Name(s)
Muscle electro-stimulation
Intervention Description
A program of intermittent hypobaric hypoxia and muscle electro-stimulation of 3 days (3 hours/day) per week during 12 weeks
Intervention Type
Other
Intervention Name(s)
Intermittent hypobaric hypoxia
Primary Outcome Measure Information:
Title
Change from initial physical stress test at one week post-intervention
Description
Physical graded maximum stress tests are performed on a cycle ergometer controlling the workload, in order to evaluate physical capacity and adaptation to different intensities of effort.While performance of these tests are conducted, cardiocirculatory (control of heart rate, blood pressure measurement, continuous ECG) and respiratory (breathing gases analysis) are monitored to observe the adaptation to the effort.
Time Frame
One week before and an expected average of one week after the intervention
Title
Change from initial psychological test at one weeks after intervention
Description
Psychological tests evaluated features of language and work (verbal memory-RAVLT), Trail Making Test (TMT A and B), Stroop Test, working memory capacity and attention (WAIS III), information processing speed (WAIS III), orientation and verbal fluency (Barcelona test), executive functions (WAIS III and Tower of London tests) and estimated premorbid intelligence index (vocabulary, WAIS III). Reduced Paced Auditory Serial Addition Test (PASAT-G)
Time Frame
One week before and an average of one week after the intervention
Secondary Outcome Measure Information:
Title
Circulating progenitor cells increase
Description
Blood CD34 staining and flow cytometry assay in accordance with ISHAGE guidelines (Keeney et al., 1998). CD34 cells/µL.
Time Frame
The day before, every 15 days during the intervention and two weeks after the intervention
Other Pre-specified Outcome Measures:
Title
Relationship between circulating progenitor cells and physical or psychological tests improvement
Description
If a statistically significant increase of circulating progenitor cells occurs and physical and/or psychological tests improvement, their relationship will be analyzed
Time Frame
An average of two weeks after intervention

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients who suffered severe TBI more than one year previously with physical or psychological sequelae. Written informed consent from patient Exclusion Criteria: Epilepsy Any medical or psychological contraindications for implementing the program of physical activity or hypobaric chamber. Inclusion in other ongoing study Refuse consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Luisa Corral, MD, PhD
Organizational Affiliation
University of Barcelona and Bellvitge University Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Casimiro F Javierre, MD, PhD
Organizational Affiliation
Universiy of Barcelona
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ginés Viscor, PhD
Organizational Affiliation
University of Barcelona
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Josep L Ventura, MD, PhD
Organizational Affiliation
Bellvitge University Hospital
Official's Role
Study Director
Facility Information:
Facility Name
University of Barcelona
City
L'Hospitalet de Llobregat
State/Province
Barcelona
ZIP/Postal Code
08907
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
19874615
Citation
Viscor G, Javierre C, Pages T, Ventura JL, Ricart A, Martin-Henao G, Azqueta C, Segura R. Combined intermittent hypoxia and surface muscle electrostimulation as a method to increase peripheral blood progenitor cell concentration. J Transl Med. 2009 Oct 29;7:91. doi: 10.1186/1479-5876-7-91.
Results Reference
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PubMed Identifier
22410278
Citation
Corral L, Javierre CF, Ventura JL, Marcos P, Herrero JI, Manez R. Impact of non-neurological complications in severe traumatic brain injury outcome. Crit Care. 2012 Dec 12;16(2):R44. doi: 10.1186/cc11243.
Results Reference
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PubMed Identifier
18236198
Citation
Corral L, Ventura JL, Herrero JI, Monfort JL, Juncadella M, Gabarros A, Bartolome C, Javierre CF, Garcia-Huete L. Improvement in GOS and GOSE scores 6 and 12 months after severe traumatic brain injury. Brain Inj. 2007 Nov;21(12):1225-31. doi: 10.1080/02699050701727460.
Results Reference
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PubMed Identifier
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Citation
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Citation
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PubMed Identifier
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Citation
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Citation
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Citation
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Citation
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Citation
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Exercise, Hypoxia and CPC in TBI Patients

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