Efficacy of Myofascial Release in Patients With Axial Spondyloarthritis.
Kata kunci
Abstrak
Deskripsi
Trial design: Controlled parallel double blind superiority clinical trial. Participants of the trial: Patients with a diagnosis of axial spondyloarthritis, of legal age, attending the rheumatology service of an outpatient clinic in the city of Bogotá. Planned trial period: The intervention per participant is designed to develop 6 therapy sessions 2 times per week over the course of 3 weeks. It is not planned to follow up the participants in time after the end of the study and treatment time. The total duration of the project will be 4 months while the necessary population is recruited to complete the sample size.
tanggal
Terakhir Diverifikasi: | 05/31/2020 |
Pertama Dikirim: | 06/05/2020 |
Perkiraan Pendaftaran Telah Dikirim: | 06/05/2020 |
Pertama Diposting: | 06/10/2020 |
Pembaruan Terakhir Dikirim: | 06/05/2020 |
Pembaruan Terakhir Diposting: | 06/10/2020 |
Tanggal Mulai Studi Sebenarnya: | 11/30/2020 |
Perkiraan Tanggal Penyelesaian Utama: | 02/28/2021 |
Perkiraan Tanggal Penyelesaian Studi: | 05/31/2021 |
Kondisi atau penyakit
Intervensi / pengobatan
Other: Myofascial release
Other: Sham Therapy
Tahap
Kelompok Lengan
Lengan | Intervensi / pengobatan |
---|---|
Experimental: Myofascial release Myofascial release or induction (MFR) is a widely used manual therapy treatment involving specifically guided, low-load, long-lasting mechanical forces to manipulate the myofascial complex, aimed at restoring optimal length, decreasing pain, and improving function. Manual therapists often use their hands using their knuckles, elbows, or other instrumental tools to slowly penetrate the layers of the fascia, using applied pressure with a few kilograms of force that can strain the restricted fascia, this implies a guided gentle stretch.
The experimental group will receive 1 examination session and 6 myofascial release sessions carried out by a physiotherapist specialized in orthopedic manual therapy, superficial and deep techniques will be applied in the cervical region, for the spinal at the level of the quadratus lumborum, sacroiliac region and upper trapezius. 2 sessions per week over the course of 3 weeks. | Other: Myofascial release Myofascial release or induction (IMF) is a widely used manual therapy treatment involving specifically guided, low-load, long-lasting mechanical forces to manipulate the myofascial complex, aimed at restoring optimal length, decreasing pain, and improving function. The experimental group will receive 1 examination session and 6 myofascial induction sessions carried out by a physiotherapist specialized in orthopedic manual therapy, superficial and deep techniques will be applied in the cervical region, for spinal at the level of the lumbar square, sacroiliac region and upper trapezius. 2 sessions per week over the course of 3 weeks. |
Sham Comparator: Sham Therapy The control group will receive 1 examination session and 6 simulated myofascial releasesessions, where a physiotherapist will apparently apply the same techniques and maneuvers of myofascial release, however, they will not follow the basic principles of technique execution, which does a procedure with a placebo effect. | Other: Sham Therapy The control group will receive 1 examination session and 6 simulated myofascial induction sessions, where a physiotherapist will apparently apply the same techniques and maneuvers of myofascial induction, however, they will not follow the basic principles of technique execution, which does a procedure with a placebo effect. |
Kriteria kelayakan
Usia yang Layak untuk Belajar | 18 Years Untuk 18 Years |
Jenis Kelamin yang Layak untuk Belajar | All |
Menerima Relawan Sehat | Iya |
Kriteria | Inclusion Criteria: - Patients with a diagnosis of ankylosing spondyloarthritis confirmed by rheumatologist regardless of the level of disease activity. - Patients with cognitive ability to follow orders. - Patients who agree to participate in the study and firm informed consent. Exclusion Criteria: - Patients receiving oral or parenteral coagulation therapy. - Pregnant women - Patients with Kinesiophobia. - Patients with previous physical therapy in the last 15 days. - Presence of active cancer, current treatment in chemo or radiotherapy. - Patients who do not wish to participate in the study |
Hasil
Ukuran Hasil Utama
1. Bath Ankylosing Spondylitis Metrology Index (BASMI) [3 weeks]
Ukuran Hasil Sekunder
1. Bath Ankylosing Spondylitis Functional Index (BASFI) [3 Weeks]
2. El Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) [3 weeks]
3. ASQoL (Ankylosing Spondylitis Quality of Life) [3 Weeks]