Therapy Clinical Trial
— MYONAMASTEOfficial title:
Myofascial Versus Conventional Physiotherapy in Post-mastectomy Patients: a Randomized Controlled Trial
Verified date | April 2020 |
Source | The Greater Poland Cancer Centre |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
A total of 61 patients who underwent total mastectomy for breast cancer with axillar lymph
dissection and adjuvant radiotherapy were enrolled in this trial.
The patients were randomized by toss of a coin to the treatment (n=30) or control (n=26)
groups; of these, 48 met all study protocol requirements, including the final assessment.
Inclusion criteria were: presence of functional difficulties in the shoulder area and/or
upper torso on the surgical side, and 2) eligibility for physiotherapy (determined by the
treating physician). Patients with recurrent disease and/or inflammatory or acute ailments
were excluded. All patients gave their informed consent to participate in the study.
The treatment group received myofascial treatment while patients in the control group
received conventional therapy consisting of exercise and massage.
Status | Completed |
Enrollment | 61 |
Est. completion date | December 31, 2014 |
Est. primary completion date | December 31, 2014 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - presence of functional difficulties in the shoulder area and/or upper torso on the surgical side - eligibility for physiotherapy (determined by the treating physician) - signed informed consent to participate in the study. Exclusion Criteria: - patients with recurrent disease and/or inflammatory or acute ailments were excluded. |
Country | Name | City | State |
---|---|---|---|
Poland | Greater Poland Cancer Centre | Poznan | Wielkopolska |
Lead Sponsor | Collaborator |
---|---|
The Greater Poland Cancer Centre |
Poland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | muscle length | muscle length with Janda's protocol Pectoralis Major - pars clavicularis - the normal length of these fibers allows the patient's arm (in an extended position close to the body) to rest below the horizontal. Pectoralis Major - pars sternocostalis - the normal length of these fibers allows the abducted the patient's arm to 90° to rest below the horizontal. Pectoralis Major - pars abdomen - the normal length of these pectoral fibers allows the abducted the patient's arm to 150° with slight external rotation to rest in a horizontal position. Latissimus dorsi - the normal length allows the arm to rest horizontally to the table with the lumbar spine flat on the table. Descending part of trapezius - the length is assessed qualitatively by noting the end-feel resistance. The normal end feel is gradual rather than abrupt. Levator scapulae - the length is assessed qualitatively by noting the end-feel resistance. The normal end feel is gradual rather than abrupt [Page et al. 2010]. |
2 years | |
Secondary | Active ROM in the shoulder joint on the surgical side | complete pathological response (pCR, pathologic Complete Response) | 2 years | |
Secondary | pathological response | ROM of the shoulder joint on the surgical side (flexion; extension; abduction; internal rotation; external rotation in horizontal flexion | 2 years | |
Secondary | Pain intensity | VAS - A tool used to help a person rate the intensity of certain sensations and feelings, such as pain. The visual analog scale for pain is a straight line with one end meaning no pain (0) and the other end meaning the worst pain imaginable (10) . A patient marks a point ( 0 to 10) on the line that matches the amount of pain she feels." | 2 years | |
Secondary | Scar mobility | Made by the centimeter measure as difference of distance from the bone point, to the most limited place in the scar. It was measured in directions: cranial (distance from the ridge of the coracoid) and in the transverse direction (the distance from the xiphoidal process). The centimeter measure was the distance from the bone point (xiphoid process and coracoid), to the most limited place in the scar (which was marked on the patient's examination card so that the measurement could be repeated to the same place | 2 years | |
Secondary | Presence of the visual dysfunction of scar (retraction) and presence of the axillary web syndrome | Was observed presence of the visual dysfunction of scar (retraction) and presence of the axillary web syndrome | 2 years |
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