Trial document





This study has been imported from ClinicalTrials.gov without additional data checks.
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  DRKS00005853

Trial Description

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Title

Effects of a Home-based Exercise Program on Low Back Pain in Employees

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Trial Acronym

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URL of the Trial

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Brief Summary in Lay Language

Evaluation of the effectiveness of an individually educated exercise program for the lower
back at home in employees over a period of 20 weeks.

We hypothesize that regular exercise for the lower back results in greater improvements of
low back strengths compared to controls.

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Brief Summary in Scientific Language

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Organizational Data

  •   DRKS00005853
  •   2015/02/19
  •   2014/01/03
  •   yes
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Secondary IDs

  •   NCT02029131  (ClinicalTrials.gov)
  •   SpoMed Low Back  (Hannover Medical School)
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Health Condition or Problem studied

  •   Healthy Volunteers With and Without Chronic Low Back Pain
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Interventions/Observational Groups

  •   Behavioral: Exercise
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Characteristics

  •   Interventional
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  •   Randomized controlled trial
  •   Blinded
  •   assessor
  •   No treatment
  •   Prevention
  •   Parallel
  •   N/A
  •   [---]*
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Primary Outcome

- Back strength (kg); time frame: At baseline and after 20 weeks; Assessed with the back-check 607 (Dr. WOLFF Sports and Prevention)

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Secondary Outcome

- Strenght at lateral flexion of the trunk (kg); time frame: At baseline and after 20 weeks; Assessed with the back-check 607 (Dr. WOLFF Sports and Prevention)
- Oswestry Low Back Pain Disability Score; time frame: At baseline and after 20 weeks; Assessed with the Oswestry Low Back Pain Disability questionaire
- Pain (scale); time frame: At baseline and after 20 weeks; Assessed with the visual analog scale
- Quality of life (score); time frame: At baseline and after 20 weeks; Assessed with the short form 36 questionaire
- Work ability index (score); time frame: At baseline and afetr 20 weeks; Assessed with the WAI questionaire
- Physical activity (score); time frame: At baseline and after 20 weeks; Assessed with the "Freiburger activity questionaire"
- Fat mass and fat-free mass (kg); time frame: At baseline and after 20 weeks; Assessed with Bio Impedance Analysis
- sick days (numbers); time frame: At baseline and after 20 weeks; sick days at work will be assessed for the 20 weeks of the active intervention and the whole year the intervention is conducted

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Countries of Recruitment

  •   Germany
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Locations of Recruitment

  •  
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Recruitment

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  •   2014/01/31
  •   210
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Inclusion Criteria

  •   Both, male and female
  •   18   Years
  •   67   Years
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Additional Inclusion Criteria

- men and women

- age between 18 and 67 years

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Exclusion Criteria

- beeing currently involved in an exercise program for the lower back

- known drug or alcohol abuse

- any disease that excludes the participation in an exercise program

- clinical relevant acute or chronic infections

- pregnant women

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Addresses

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    • Hannover Medical School
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    •   [---]*
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Sources of Monetary or Material Support

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    • Bitte wenden Sie sich an den Sponsor / Please refer to primary sponsor
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    •   [---]*
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Status

  •   Recruiting complete, follow-up continuing
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Trial Publications, Results and other Documents

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The parameters in ClinicalTrials.gov and DRKS are not identical. Therefore the data import from ClinicalTrials.gov required adjustments. For full details please see the DRKS FAQs .
  •   1
  •   2014/02/23
* This entry means the parameter is not applicable or has not been set.