Clinical Trials Directory

Trials / Completed

CompletedNCT05022823

Exercise and Compression for Lymphedema

Decongestive Progressive Resistance Exercise With Advanced Compression for Breast Cancer Related Lymphedema Management (DREAM): A Randomized Control Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
AHS Cancer Control Alberta · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to investigate the benefit of combining resistance exercise with use of a compression sleeve on arm lymphedema. In the study, participants will be taught a resistance exercise that follows the decongestive exercise sequence. This program is called "decongestive progressive resistance exercise" (DPRE). To evaluate the benefit from use of a compression garment on the arm. Some participants will wear their usual compression sleeve during exercise and others will use an adjustable compression wrap. The investigators hope to see if this type of combined program is helpful for women with lymphedema. The investigators also want to see if there are benefits from the addition of use of an adjustable compression wrap during exercise over use of a regularly prescribed compression sleeve.

Conditions

Interventions

TypeNameDescription
DEVICECompression sleeve, worn during exerciseParticipants wear their daytime compression sleeve during the DPRE program.
DEVICEAdjustable Compression (AC) garment, worn during exerciseParticipants wear an Adjustable Compression (AC) garment during the DPRE program. Participants will be fitted for an Adjustable Compression garment and instructed in its application by a physical therapist.
DEVICECompression sleeve, daytime wearCompression sleeve worn for at least 12 hours per day, seven days a week.
BEHAVIORALDecongestive Progressive Resistance Exercise programSupervised DPRE exercise program, twice a week for 12 weeks. Exercises will be individualized and offered in a group-based format. After the 12-week intervention, participants will continue the same program (independently) twice weekly for an additional 12 weeks at home or in a community-based fitness center or attend supervised group exercise sessions virtually.
BEHAVIORALHome exercise programParticipants are provided with a home exercise program that follows the decongestive exercise sequence and instructed to perform the exercise sequence once daily for a 10-15 minute period.

Timeline

Start date
2022-06-29
Primary completion
2024-02-08
Completion
2024-02-08
First posted
2021-08-26
Last updated
2025-06-27

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT05022823. Inclusion in this directory is not an endorsement.