TCECAM: Exercise, Hypoxia and CPC in TBI Patients

Sponsor
University of Barcelona (Other)
Overall Status
Completed
CT.gov ID
NCT02083445
Collaborator
Ministerio de Economía y Competitividad, Spain (Other)
21
1
3
27
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Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Other: cognitive activities
  • Other: Exercise program
  • Device: Muscle electro-stimulation
  • Other: Intermittent hypobaric hypoxia
N/A

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.

Study Design

Study Type:
Interventional
Actual Enrollment :
21 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Exercise, Muscle Electro-stimulation and Intermittent Hypobaric Hypoxia Program and Circulating Progenitor Cells in Traumatic Brain Injured Patients
Study Start Date :
Nov 1, 2011
Actual Primary Completion Date :
Dec 1, 2013
Actual Study Completion Date :
Feb 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Control group

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.

Other: cognitive activities
Participants followed a day of cognitive activities 1 day (1 hour/day) per week during 12 weeks.

Active Comparator: Exercise group

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.

Other: Exercise program
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.

Active Comparator: Muscle electro-stimulation and IHH

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.

Device: Muscle electro-stimulation
A program of intermittent hypobaric hypoxia and muscle electro-stimulation of 3 days (3 hours/day) per week during 12 weeks

Other: Intermittent hypobaric hypoxia

Outcome Measures

Primary Outcome Measures

  1. Change from initial physical stress test at one week post-intervention [One week before and an expected average of one week after the 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.

  2. Change from initial psychological test at one weeks after intervention [One week before and an average of one week after the 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

  1. Circulating progenitor cells increase [The day before, every 15 days during the intervention and two weeks after the intervention]

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

Other Outcome Measures

  1. Relationship between circulating progenitor cells and physical or psychological tests improvement [An average of two weeks after intervention]

    If a statistically significant increase of circulating progenitor cells occurs and physical and/or psychological tests improvement, their relationship will be analyzed

Eligibility Criteria

Criteria

Ages Eligible for Study:
20 Years to 60 Years
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Barcelona L'Hospitalet de Llobregat Barcelona Spain 08907

Sponsors and Collaborators

  • University of Barcelona
  • Ministerio de Economía y Competitividad, Spain

Investigators

  • Principal Investigator: Luisa Corral, MD, PhD, University of Barcelona and Bellvitge University Hospital
  • Study Director: Casimiro F Javierre, MD, PhD, Universiy of Barcelona
  • Study Chair: Ginés Viscor, PhD, University of Barcelona
  • Study Director: Josep L Ventura, MD, PhD, Bellvitge University Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Luisa Corral, Luisa Corral, University of Barcelona
ClinicalTrials.gov Identifier:
NCT02083445
Other Study ID Numbers:
  • DEP2010-222005-C02-02
  • AC048-10, PR017/10
First Posted:
Mar 11, 2014
Last Update Posted:
Mar 11, 2014
Last Verified:
Mar 1, 2014
Keywords provided by Luisa Corral, Luisa Corral, University of Barcelona
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 11, 2014