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Effects of High-intensity Interval Training in Patients in Hemodialysis (OsloExDia)

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ClinicalTrials.gov Identifier: NCT01728415
Recruitment Status : Unknown
Verified September 2014 by Birgitta Blakstad Nilsson, PhD, Oslo University Hospital.
Recruitment status was:  Recruiting
First Posted : November 19, 2012
Last Update Posted : September 22, 2014
Sponsor:
Collaborator:
Norwegian Fund for Postgraduate Training in Physiotherapy
Information provided by (Responsible Party):
Birgitta Blakstad Nilsson, PhD, Oslo University Hospital

Brief Summary:
The purpose of this study is to evaluate the effects of high intensity interval training compared to moderate exercise training and a control group on exercise capacity and quality of life in patients with end stage renal disease on hemodialysis.

Condition or disease Intervention/treatment Phase
Chronic Renal Disease Other: exercise Not Applicable

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 18 participants
Allocation: Randomized
Intervention Model: Factorial Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Effects of High-intensity Interval Training in Patients in Hemodialysis
Study Start Date : October 2012
Estimated Primary Completion Date : December 2014
Estimated Study Completion Date : September 2016

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: A: Exercise
High intensity interval exercise training (3 x 3 minutes of intensity abow 85% og Heart rate peak)
Other: exercise
Group A: high intensity exercise training Group B: moderate intensity exercise training C: Control group

Active Comparator: B: Execise
Moderate continuous exercise training
Other: exercise
Group A: high intensity exercise training Group B: moderate intensity exercise training C: Control group

No Intervention: C: Controll
Usual care without exercise training



Primary Outcome Measures :
  1. Peak oxygen uptake [ Time Frame: baseline, 16 weeks ]
    Canges from baseline in peak oxygen uptake at 16 weeks



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Ages Eligible for Study:   20 Years to 75 Years   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients on hemodialysis ≥ 3 months

Exclusion Criteria:

  • Acute infection
  • Systolic BP>180 mmHG or diabolic BP>105 mmHG
  • Unstable angina pectoris
  • Serious rhythm disturbances
  • Hyperkalemic (> 6 mmol/L),
  • Unstable diabetes mellitus
  • Wheelchair
  • Dialyses access on lower extremities
  • Haemoglobin < 9 g/dl

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01728415


Contacts
Contact: Birgitta Blakstad Nilsson, PhD +4793210913 b.b.nilsson@medisin.uio.no
Contact: Aud Eldrid Stenehjem, PhD +4790667069 uxaust@ous-hf.no

Locations
Norway
Oslo University Hospital Recruiting
Oslo, Postboks 4950 Nydalen, Norway, 0424
Contact: Birgitta Blakstad Nilsson, PhD    +47 93210913      
Principal Investigator: Heidi B Næss         
Sponsors and Collaborators
Oslo University Hospital
Norwegian Fund for Postgraduate Training in Physiotherapy

Responsible Party: Birgitta Blakstad Nilsson, PhD, The Oslo ExDia-study, Oslo University Hospital
ClinicalTrials.gov Identifier: NCT01728415     History of Changes
Other Study ID Numbers: 2012/1459
126/12-303.0 ( Other Grant/Funding Number: The Norwegian Fund for Post-Graduate Training in Physiotherapy )
First Posted: November 19, 2012    Key Record Dates
Last Update Posted: September 22, 2014
Last Verified: September 2014

Keywords provided by Birgitta Blakstad Nilsson, PhD, Oslo University Hospital:
Exercise
Hemodialysis
Physical therapy
high-intensity

Additional relevant MeSH terms:
Renal Insufficiency, Chronic
Kidney Failure, Chronic
Renal Insufficiency
Kidney Diseases
Urologic Diseases