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临床试验/NCT04944446
NCT04944446已完成不适用

Effectiveness of Myofascial Release in Pathologies of the Shoulder

University of Cadiz1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2018年9月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
44
试验地点
1
主要终点
Degree of pain

研究概览

简要总结

Shoulder pathology has a high prevalence in the field of musculoskeletal diagnoses, as well as being a common etiology in cases of disability. Passive and active-assisted kinesitherapy are used in the physiotherapy protocol. These techniques sometimes lead to feedback of fear and increased sensation of pain on the part of the patient that can slow or hinder the optimal recovery. A randomized clinical trial is intended to demonstrate that techniques for myofascial release of muscles important in the biomechanics of the shoulder, it is more effective than kinesitherapy in improving myofascial and also by eliminating the aforementioned unwanted effects and, therefore, improving the recovery of these processes.

详细描述

The purpose of this study was to compare the efficacy of myofascial therapy and kinesitherapy in improving function in shoulder pathology with prolonged immobilization. Design Prospective, single-blind randomized controlled trial. Setting Inpatient department of a secondary university hospital. Participants Shoulder pain patients (N=44) were consecutively recruited and randomly assigned to an intervention or control group. Interventions Patients were randomly assigned to a Control Group, to which conventional kinesitherapy was applied, or to the intervention group to which a Myofascial therapy protocol was applied. Both groups completed a therapeutic exercise program based on specific mobilization and strengthening exercises. Main Outcome Measures The QuickDash questionnaire was the primary outcome, visual analog scale and the passive range of motion of the shoulder joint, grades were the secondary outcomes. The outcomes were evaluated at baseline (T0) and at 4 (T2),

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

盲法说明

Double (Participant, Outcomes Assessor) external evaluator

入排标准

年龄范围
20 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Be between 20 and 80 years old.
  • •Patients who have been immobilized due to the following diagnoses: Suture of the rotator cuff or fracture of the proximal extremity of the humerus.
  • •Have signed the informed consent of acceptance in the participation of the study

排除标准

  • •Present neurological pathology.
  • •Be subdued corticoid therapy.
  • •Have anticoagulant treatment or have had it less than a month ago.
  • •Insulin-dependent diabetic patients.
  • •Patients with hemophilia.
  • •Having diagnosed a psychological or psychiatric pathology.
  • •Non-intervened displaced humerus fractures.

研究组 & 干预措施

Group myofascial treatment

Experimental

The trial group will also be referred by the rehabilitating doctor to the physiotherapy room, these patients will be treated by two physiotherapists with training in myofascial release therapy with which they will carry out a treatment protocol that will consist of myofascial release of the shoulder blade angle, subscapularis and global pectoral technique as well as superficial myofascial release of said musculature with a during 12-15 minutes, in addition to a 30-minute session of active kinesitherapy with exercises and mechanotherapy. Same as the control group.

These mobilizations are carried out in the absence of pain, although the difference between joint tension or stretching and pain is explained to the patient.

干预措施: Treatment (Other)

Group Kinesitherapy treatment

Active Comparator

This group will be treated in a protocolized way with techniques such as passive kinesitherapy, active-assisted and active kinesitherapy to win mobility.

They consist of mobilizing the affected arm in the movements of flexion (upward), separation (towards the outer side) and rotation, these lateral decubitus (bring the hand to the nape of the neck) and internal (bring the hand to the lower back) trying to win joint amplitude.

These mobilizations are performed in the absence of pain, although the difference between joint tension or stretching and pain will be explained to the patient. The treatment will be carried out as usual with a duration of about 12-15 minutes of mobilization and about 30 minutes of active kinesitherapy with exercises and mechanotherapy, these consist of active shoulder mobility exercises. Emphasis will be placed on working with the pain threshold so as not to cause damage or negative nociceptive reactions.

干预措施: Treatment (Other)

结局指标

主要结局

Degree of pain

时间窗: Change from Baseline at 4 weeks

Visual Analog Scale

Functional capacity

时间窗: Change from Baseline at 4 weeks

Dash Scale. Minimum: 0 Maximum: 100. Higher scores mean a worse outcome

Shoulder joint mobility

时间窗: Change from Baseline at 4 weeks

Goniometer Records

Functional capacity

时间窗: Baseline

Dash Scale. Minimum: 0 Maximum: 100. Higher scores mean a worse outcome

Shoulder joint mobility

时间窗: Baseline

Goniometer Records

Degree of pain

时间窗: Baseline

Visual Analog Scale. Minimum: 0 Maximum: 10. Higher scores mean a worse outcome

次要结局

  • Age(Baseline)
  • Sex(Baseline)
  • Pathology of access to the study(Baseline)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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