HoBIDnurse: Home-based vs Intradialysis Exercise Guided by Nursing Staff

Sponsor
Cardenal Herrera University (Other)
Overall Status
Completed
CT.gov ID
NCT04051515
Collaborator
Hospital de Manises (Other)
70
7
2
3.7
10
2.7

Study Details

Study Description

Brief Summary

Participants will be randomized either to home-based exercise or to intradialysis exercise guided by nurses of the renal unit. The programs will last 16 weeks. The intradialysis exercise consists of combined aerobic and resistance training exercise. The home-based exercise consists of resistance exercise and walking.

Condition or Disease Intervention/Treatment Phase
  • Other: Intradialysis exercise training
  • Other: Home-based exercise training
N/A

Detailed Description

During 16 weeks one group will follow an intradialysis exercise program. The exercise program consists of strengthening exercises for lower limbs and for the upper limb free of fistula. The exercise program includes isotonic exercises for quadriceps, triceps surae, psoas, glutei, and brachial biceps; and isometric exercises for hip adductors and hamstrings. Elastic bands will be used to apply resistance. Progression will be achieved by increasing from 1 set of 10 repetitions until 3 sets of 15 repetitions. This first part of the exercise session will last no more than 30 minutes. The program will also include aerobic exercise (cycling) for up to 30 minutes. Intensity will adapted through the duration of the study so that the participant feel the exercise from hard to somewhat hard (13 to 15 at the rate of perceived exertion 6 to 20). Time and resistance will be adapted progressively. After an initial training period by a physiotherapist, the nursing staff will be responsible for monitoring and implementing the program.

The other group will follow a home-based program. A booklet with resistance exercise and recommendation of walking between exercises will be provided. An initial training phase will be applied by the physiotherapists from the rehabilitation department.

Study Design

Study Type:
Interventional
Actual Enrollment :
70 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Participants will be randomized into one of two exercise groups, intradialysis or home-based programParticipants will be randomized into one of two exercise groups, intradialysis or home-based program
Masking:
Double (Investigator, Outcomes Assessor)
Masking Description:
A team of assessors, different from the researchers implementing the exercise, will record all dependent variables. A blind researcher will randomize participants
Primary Purpose:
Treatment
Official Title:
Home-based vs Intradialysis Exercise Program Guided by Nursing Staff
Actual Study Start Date :
Aug 9, 2019
Actual Primary Completion Date :
Nov 29, 2019
Actual Study Completion Date :
Nov 29, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intradialysis exercise guided by nursing staff

During 16 weeks subjects will exercise during the hemodialysis session, the exercise will include both aerobic and resistance training. Guidance will be provided by nursing staff

Other: Intradialysis exercise training
Combined exercise, aerobic and resistance training, implemented by nursing staff

Active Comparator: Home-based exercise program

During 16 weeks subjects will exercise on their own at home. A booklet will be provided, with a diary. Instructions to do resistance exercise with intervals of walking will be provided. Initial training will be provided by physiotherapy staff from the hospital.

Other: Home-based exercise training
Combined exercise, aerobic and resistance training, implemented independently home

Outcome Measures

Primary Outcome Measures

  1. Change from baseline short physical performance battery at 16 weeks [Baseline, 16 weeks]

    Score achieved at the battery that includes balance tests (4 points), sit to stand to sit 5 (4 points) and and gait speed (4 points). The total score is calculated , from 1 to 12, being 12 the highest functional score

  2. Change from baseline gait speed at 16 weeks [Baseline, 16 weeks]

    Speed to cover 4 meters, in meters/second

Secondary Outcome Measures

  1. Change from baseline sit to stand 10 test at 16 weeks [Baseline, 16 weeks]

    Time to perform 10 repetitions sit to stand

  2. Change from baseline sit to stand 60 test at 16 weeks [Baseline, 16 weeks]

    Sit to stand repetitions performed in 60 seconds

  3. Change from baseline 6 minutes walk test at 16 weeks [Baseline, 16 weeks]

    Number of meters walked in 6 minutes

  4. Change from baseline handgrip strength at 16 weeks [Baseline, 16 weeks]

    Bilateral handgrip strength

  5. Change from baseline one-leg heel rise test at 16 weeks [Baseline, 16 weeks]

    Number of heel rise repetitions achieved

  6. Change from baseline one-leg standing test at 16 weeks [Baseline, 16 weeks]

    Time achieved while standing on one leg

  7. Change from baseline timed up and go test at 16 weeks [Baseline, 16 weeks]

    Time to stand up, walk 3 meters, come back and sit down again

  8. Change from baseline Physical activity level at 16 weeks [Baseline, 16 weeks]

    Physical activity questionnaires

  9. Change from baseline Health related quality of life at 16 weeks [Baseline, 16 weeks]

    Medical outcomes survey Short Form 36 questionnaire to measure health-related quality of life, rated from 0 to 100, being the highest score the better the quality of life

  10. Adherence, as number of sessions performed /number of sessions offered [16 weeks]

    Sessions performed/sessions offered

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Patients on hemodialysis medically stable, be able to walk at least a few steps, even if you need walking aids like canes or a walker. Life expectancy greater than 6 months

Exclusion Criteria:
  1. Myocardial infarction in the previous 6 weeks

  2. Angina unstable on exercise or at rest

  3. Brain injury derived from a cardiovascular problem. Cerebral vascular disease such as stroke in the last 6 months or with relevant sequelae in lower limb mobility presenting hemiparesia.

  4. Life expectancy less than 6 months

  5. Cognitive impairment

  6. Language barriers

  7. Illiteracy

Contacts and Locations

Locations

Site City State Country Postal Code
1 KU Leuven Leuven Belgium 3000
2 Aristotle University of Thessaloniki Thessaloníki Greece 57001
3 Hospital de Manises Manises Valencia Spain 46940
4 Universitat de Valencia Valencia Spain 46010
5 Universiat de Valéncia Valencia Spain 46022
6 Skane Univeristy Hospital Lund Sweden
7 Karolinska Institute Stockholm Sweden 14186

Sponsors and Collaborators

  • Cardenal Herrera University
  • Hospital de Manises

Investigators

  • Principal Investigator: Eva Segura-Ortí, PhD, Universidad CEU Cardenal Herrera, UCH CEU

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Eva Segura Ortí, Professor, Cardenal Herrera University
ClinicalTrials.gov Identifier:
NCT04051515
Other Study ID Numbers:
  • HoBIDnurse
First Posted:
Aug 9, 2019
Last Update Posted:
Jan 29, 2021
Last Verified:
Jan 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Eva Segura Ortí, Professor, Cardenal Herrera University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 29, 2021