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Exercise therapy on cording after breast cancer surgery

Physical therapy treatment of axillary web syndrome dysfunctions: a randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-5h983f
Enrollment
Unknown
Registered
2019-03-28
Start date
2019-05-14
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast neoplasms

Interventions

Intervention Group (IG): Therapeutic exercise (active, active assisted and stretching exercises). Sessions once a week, during the four week period. (30 participants) Control group (CG): No interven
Other
E02.760.169.063.500.387
H02.010.625
E02.779.474

Sponsors

Hospital Universitário de Brasília
Lead Sponsor
Universidade de Brasilia
Collaborator

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Women over 18 years old; who underwent unilateral breast cancer surgery; with reduced range of motion compared to the contralateral limb due to axillary web syndrome; with pain in the upper limb due to axillary web syndrome.

Exclusion criteria

Exclusion criteria: Inability to read; stage IV breast cancer; lymphedema; active infection in the area to be treated; dehiscence; deep venous thrombosis; physical or mental conditions that interfere in the assessment and / or treatment proposal; unavailability for weekly physiotherapeutic intervention for four weeks.

Design outcomes

Primary

MeasureTime frame
Shoulder range of motion assessed by a universal goniometer. It will be evaluated before the intervention (baseline) and at the end of the intervention (4 weeks).;Pain measured by Numerical Rating Scale and Visual Analog Scale. It will be evaluated before the intervention (baseline) and at the end of the intervention (4 weeks).

Secondary

MeasureTime frame
Upper limb function, evaluated by Disabilies of the Arm Shoulder and Hand (DASH) questionnaire. Evaluated before the intervention (baseline)and at the end of the intervention (4 weeks).;Quality of life measured by European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core -30 (EORTC QLQ-C30) and Quality of Life Questionnaire- Breast Cancer (EORT QLQ-BR23). Evaluated before the intervention (baseline) and at the end of the intervention (4 weeks).;Patient satisfaction with treatment evaluated by Numerical Rating Scale. Evaluated at the end of the intervention (4 weeks).;Stretching sensation in upper limb, evaluated by Numerical Rating Scale. It will be evaluated before the intervention (baseline) and at the end of the intervention (4 weeks).;Presence of cord: visible and/ or palpable, evaluated by physical exam before the intervention (baseline) and at the end of the intervention (4 weeks).

Countries

Brazil

Contacts

Public ContactLiana Matheus

Universidade de Brasilia

lbgomide@yahoo.com.br5561982205050

Outcome results

None listed

Source: REBEC (via WHO ICTRP)