Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04369079
Other study ID # MYONAMASTE
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 1, 2013
Est. completion date December 31, 2014

Study information

Verified date April 2020
Source The Greater Poland Cancer Centre
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Description:

Treatment duration in both groups was a mean of 4 weeks. Therapy was performed daily excluding weekends and consisted of 45 minutes of individual work with an oncological physiotherapist. In the treatment group, manual myofascial techniques were used to decrease muscle tension and increase elasticity of the soft tissues in the surgical area as well as in tissues that could affect range of motion (ROM) and cause pain. Fascial techniques were used together with the following techniques: deep massage of neck and shoulder girdle muscles; trigger point therapy; tissue scar treatment in the vicinity of the scar and directly on the scar, by stretching, breaking, pulling, as well as static and dynamic rolling; post-isometric relaxation (stretching) of shoulder and neck muscles; active release technique of the chest and shoulder; selected fascial distortion model techniques; and fascial manipulation techniques consisting of developing specific CC-center of coordination and CF-center of fusion points in the operated area and the shoulder on the same side. The exact sequence and number of procedures differed in each patient according to need as determined by prior functional examination. The control group underwent kinesiotherapeutic procedures that included various floor gymnastic exercises with gymnastic stick, balls, and/or elastic tapes, conventional massage of neck and shoulder girdle muscles and therapeutic exercises to increase ROM in the upper limb and in the chest area. Both groups before or after every of the treatment procedure underwent ten-minute manual lymphatic drainage in the limb on the mastectomy side.

Patient interviews and diagnostic examinations were performed at baseline (pre-treatment) and after treatment finalization. The following variables were assessed during the diagnostic examination of the 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.


Recruitment information / eligibility

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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
manual myofascial techniques
Fascial techniques were used together with the following techniques: deep massage of neck and shoulder girdle muscles; trigger point therapy; tissue scar treatment in the vicinity of the scar and directly on the scar, by stretching, breaking, pulling, as well as static and dynamic rolling; post-isometric relaxation (stretching) of shoulder and neck muscles; active release technique of the chest and shoulder; selected fascial distortion model techniques; and fascial manipulation techniques consisting of developing specific CC-center of coordination and CF-center of fusion points in the operated area and the shoulder on the same side.
conventional therapy consisting of exercise and massage.
Underwent kinesiotherapeutic procedures that included various floor gymnastic exercises with gymnastic stick, balls, and/or elastic tapes, conventional massage of neck and shoulder girdle muscles and therapeutic exercises to increase ROM in the upper limb and in the chest area.

Locations

Country Name City State
Poland Greater Poland Cancer Centre Poznan Wielkopolska

Sponsors (1)

Lead Sponsor Collaborator
The Greater Poland Cancer Centre

Country where clinical trial is conducted

Poland, 

Outcome

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
See also
  Status Clinical Trial Phase
Completed NCT03650543 - Effect of the CYP2C19 Polymorphism in Helicobacter Pylori Eradication Phase 4
Recruiting NCT05788861 - Invasive Group A Streptococcal Infection
Completed NCT03712748 - Online Imaginal Exposure N/A
Completed NCT01031667 - Synergistic Effect of Combination Therapy With Cilostazol and Probucol on Plaque Stabilization and Lesion Regression: Serial Intravascular Ultrasound and Virtual Histology Study(SECURE Study) Phase 4
Recruiting NCT00226408 - Standard High-Dose Alpha Interferon Versus Intermittent High-Dose Alpha Interferon Phase 3
Completed NCT05104957 - Evaluation of the Kinesiology Taping Effectiveness in the Treatment of Lumbar Spine Pain N/A
Recruiting NCT06137053 - Effect of Telitacicept on Transitional Regulatory B Cells in Patients With Systemic Lupus Erythematosus
Completed NCT01023126 - Obesity and Psychotherapy as an Alternative to Treatment N/A
Not yet recruiting NCT06413407 - Tai Chi Exercise and Receptive Music Therapy for the Elderly N/A
Recruiting NCT06040515 - Probiotic After Acute Colonic Diverticulitis
Recruiting NCT05340738 - AI-Based Fidelity Feedback to Enhance CBT N/A
Active, not recruiting NCT02455609 - Intrathecal Ketamine, Dexmedetomidine and Both With Bupivacaine for Postoperative Abdominal Cancer Surgery Pain Phase 2/Phase 3
Completed NCT05261503 - Investigation of the Effectiveness of Environmental Enrichment-Based Intervention in Preterm Infants N/A
Completed NCT04926311 - Efficiency of Speech and Language Intervention on Achievement of Children With Developmental Language Disorder
Recruiting NCT03721783 - Infant and Child European Cryoablation Project ICECaP
Recruiting NCT03283839 - Consequences of Temporomandibular Disorder on Balance Control N/A
Recruiting NCT05901558 - Strategies for Toddler ASD With Remote-therapy (STAR) Model for ASD N/A
Completed NCT03177863 - Expectancy as Alternative to Treatment for Cervical Intraepithelial Neoplasia Grade 2 Among Women 25 - 30 Years of Age N/A
Recruiting NCT06146972 - Efficacy Study of Iguratimod Combined With Tofacitab in Patients With RF Positive/Negative Rheumatoid Arthritis Phase 4
Recruiting NCT03161249 - Psychoeducative Treatment of FEP With Mobile Training N/A