Exercise Training Study of Patients With Claudicatio Intermittens

NCT06448390 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 100

Last updated 2025-06-06

No results posted yet for this study

Summary

The aim of the study is to evaluate whether walking capacity in patients with intermittent claudication is improved more by home-based 5+ exercise training than by current recommendations of daily walking.

Conditions

  • Claudication, Intermittent

Interventions

BEHAVIORAL

Physical training

The patients are randomized to either walking 30 minutes 3 times a week or lifting the body to a tip toe position three times a day until pain in the claves and then add another five liftings before ending the session

Sponsors & Collaborators

  • Sykehuset i Vestfold HF

    collaborator OTHER
  • Oslo University Hospital

    collaborator OTHER
  • Haukeland University Hospital

    collaborator OTHER
  • Sorlandet Hospital HF

    collaborator OTHER_GOV
  • St. Olavs Hospital

    collaborator OTHER
  • Sykehuset Ostfold

    collaborator OTHER
  • Helse Stavanger HF

    collaborator OTHER_GOV
  • Sykehuset Innlandet HF

    collaborator OTHER
  • Drammen sykehus

    collaborator OTHER
  • Alesund Hospital

    collaborator OTHER
  • Sahlgrenska University Hospital

    collaborator OTHER
  • Karolinska Institutet

    collaborator OTHER
  • University Hospital, Linkoeping

    collaborator OTHER
  • Norwegian University of Science and Technology

    lead OTHER

Principal Investigators

  • Joakim Nordanstig, Professor · Sahlgrenska University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
DOUBLE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-01
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • Norway
  • Sweden

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06448390 on ClinicalTrials.gov