High Intensity Interval Training (HIIT) for Patients With Cancer-related Lymphedema in the Lower Limbs

NCT03653819 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2018-11-15

No results posted yet for this study

Summary

The aim of the study is to explore the feasibility and safety of High Intensity Interval Training on a stationary bike for patients with lymphedema in the lower limbs and the role of compression garments during exercise.

The design of the study is a cross-over randomized clinical trial. Participants will be randomized into two groups. Both will perform two separate exercise sessions.Group A will perform the first exercise with compression garment and the second session without compression garment, with wash-out period of 1 week between sessions. Group B will perform the exercise sessions in the opposite order.

Conditions

  • Lymphedema of Leg
  • Cancer of Cervix
  • Cancer, Ovarian
  • Cancer, Endometrial
  • Cancer of the Prostate
  • Malignant Melanoma

Interventions

OTHER

First exercise session + compression

The Interval Training consists of a 5 minute warm-up on the stationary bike followed by 7 intervals of cycling for 1 minute at level 15-16 on the Borg Scale of Perceived Exertion. Inbetween intervals, participants reduce resistance on the stationary bike and pedals for 1 minute at level 11-12 on the Borg Scale. The session ends with a 5-10 minute cool-down pedaling and stretching exercises for the lower limbs.

OTHER

First exercise session - compression

The Interval Training consists of a 5 minute warm-up on the stationary bike followed by 7 intervals of cycling for 1 minute at level 15-16 on the Borg Scale of Perceived Exertion. Inbetween intervals, participants reduce resistance on the stationary bike and pedals for 1 minute at level 11-12 on the Borg Scale. The session ends with a 5-10 minute cool-down pedaling and stretching exercises for the lower limbs.

Sponsors & Collaborators

  • University of Copenhagen

    collaborator OTHER
  • Herlev and Gentofte Hospital

    lead OTHER

Principal Investigators

  • Merete C Wittenkamp, PT · Department of Physiotherapy and Occupational Therapy at Herlev and Gentofte Hospital,

  • Carsten B Juhl, PT MPH PhD · Department of Physiotherapy and Occupational Therapy, Herlev and Gentofte Hospital/Research Unit for Musculoskeletal Function and Physiotherapy, University of Southern Denmark.

  • Anders Vinther, PT MSc PhD · Department of Physiotherapy and Occupational Therapy, Herlev and Gentofte Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-09-06
Primary Completion
2018-11-13
Completion
2018-11-13

Countries

  • Denmark

Study Locations

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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 NCT03653819 on ClinicalTrials.gov