Does local immersion in Thermo-Neutral Bath influence surface ElectroMyoGraphy measurements? Results of an experimental trial

ISRCTN ISRCTN86475982
DOI https://doi.org/10.1186/ISRCTN86475982
Secondary identifying numbers 20 February 2004
Submission date
09/02/2007
Registration date
13/04/2007
Last edited
08/08/2011
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Other
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Not provided at time of registration

Contact information

Dr Banu Kalpakcioglu
Scientific

Haydarpasa Numune Hastanesi Fiziksel Týp ve Rehabilitasyon Klinigi
Haydarpasa
Istanbul
34668
Türkiye

Study information

Study designExperimental study on healthy individuals
Primary study designInterventional
Secondary study designOther
Study setting(s)Other
Study typeDiagnostic
Scientific title
Study acronymTNB-sEMG
Study objectivesDoes thermo-neutral whole body immersion into water influence the measurement of surface Electromyography (EMG)?
Ethics approval(s)Ethics approval was not sought for this trial. All subjects were informed about the study and written consent forms were provided from each of them.
Health condition(s) or problem(s) studiedHealthy individuals
InterventionAll participants received the same intervention. Each participant immersed his/her forearm in the thermo-neutral bath for one minute. In order to see the effect of the immersion on the participants, EMG measurements were made before and after the immersion process.
Intervention typeOther
Primary outcome measureTo measure thermo-neutral whole body immersion effect on measurements of surface electromyography on healthy subjects.
Secondary outcome measuresEfficacy of thermo-neutral whole body immersion on measurements of surface electromyography on healthy subjects.
Overall study start date14/04/2005
Completion date25/05/2006

Eligibility

Participant type(s)Patient
Age groupAdult
Lower age limit18 Years
SexNot Specified
Target number of participants11 healthy subjects
Key inclusion criteriaHealthy subjects over 18 years of age and who have given written informed consents.
Key exclusion criteria1. Subjects with any neurosensorial and/or muscular disease
2. Subjects on sedative treatments and/or on any medications for any reasons
Date of first enrolment14/04/2005
Date of final enrolment25/05/2006

Locations

Countries of recruitment

  • Germany
  • Türkiye

Study participating centre

Haydarpasa Numune Hastanesi Fiziksel Týp ve Rehabilitasyon Klinigi
Istanbul
34668
Türkiye

Sponsor information

Individual sponsor (Germany)
Other

c/o Dr Banu Kalpakcioglu
Haydarpasa Numune Hastanesi Fiziksel Týp ve Rehabilitasyon Klinigi
Haydarpasa
Turkey
Istanbul
34668
Türkiye

Funders

Funder type

Other

Investigator-funded trial

No information available

Results and Publications

Intention to publish date
Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot provided at time of registration
Publication and dissemination planNot provided at time of registration
IPD sharing plan