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
| Type | Name | Description |
|---|---|---|
| DEVICE | Compression sleeve, worn during exercise | Participants wear their daytime compression sleeve during the DPRE program. |
| DEVICE | Adjustable Compression (AC) garment, worn during exercise | Participants 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. |
| DEVICE | Compression sleeve, daytime wear | Compression sleeve worn for at least 12 hours per day, seven days a week. |
| BEHAVIORAL | Decongestive Progressive Resistance Exercise program | Supervised 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. |
| BEHAVIORAL | Home exercise program | Participants 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.