This study evaluates whether strain counterstrain therapy affects pain, fatigue, psychological status, and quality of life in women diagnosed with fibromyalgia. Participants are assigned to one of three groups: a control group, a conservative treatment group, or a conservative treatment plus strain counterstrain therapy group. Treatment sessions are conducted five days per week for three weeks. Outcomes are assessed before and after the intervention using validated measurement scales. The purpose is to compare changes among groups and determine the effects of adding strain counterstrain therapy to conservative treatment.
Fibromyalgia is a chronic condition characterized by widespread pain, fatigue, and functional limitations that may negatively affect psychological well-being and quality of life. Nonpharmacological approaches are commonly used in management and may support symptom control and functional improvement. Manual therapy techniques are among the interventions applied to address musculoskeletal symptoms. This study is designed to investigate the effects of strain counterstrain therapy in individuals diagnosed with fibromyalgia. Participants are assigned to different intervention groups receiving either standard care alone or standard care combined with a manual therapy approach. The intervention is administered according to a structured treatment protocol over a defined study period. Outcome measures evaluate changes in pain, fatigue, psychological status, and quality of life using validated assessment instruments.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
105
The conservative physiotherapy program consists of standard physical therapy modalities applied according to a structured treatment protocol. Sessions are conducted five days per week for three weeks and include routinely used physiotherapy approaches intended to support symptom management and functional improvement.
Strain counterstrain therapy is a manual therapy technique applied by a trained therapist using passive positioning methods intended to reduce musculoskeletal tenderness and improve comfort. The intervention is administered according to a structured treatment protocol during scheduled sessions over the study period.
Inonu University Turgut Ozal Medical Center
Malatya, Turkey (Türkiye)
Change in Pain Intensity (Visual Analog Scale)
Pain intensity is assessed using the Visual Analog Scale (VAS), a validated measure consisting of a 10-cm line ranging from 0 (no pain) to 10 (worst imaginable pain). Participants indicate their pain level on the scale, and change is calculated as the difference between pre-intervention and post-intervention scores.
Time frame: Baseline and immediately after completion of the 3-week intervention period
Change in Fatigue Severity Score (Fatigue Severity Scale)
Fatigue is assessed using the Fatigue Severity Scale (FSS), a validated self-report questionnaire used to evaluate the impact of fatigue on daily functioning. Scores are calculated according to the instrument instructions, with higher scores indicating greater fatigue severity. Change is calculated as the difference between pre-intervention and post-intervention scores.
Time frame: Baseline and immediately after completion of the 3-week intervention period
Change in Depression Score (Beck Depression Inventory)
Depression is assessed using the Beck Depression Inventory, a validated self-report questionnaire used to measure the severity of depressive symptoms. Scores are calculated according to the instrument guidelines, with higher scores indicating greater depression severity. Change is calculated as the difference between pre-intervention and post-intervention scores.
Time frame: Baseline and immediately after completion of the 3-week intervention period
Change in Anxiety Score (Beck Anxiety Inventory)
Anxiety is assessed using the Beck Anxiety Inventory, a validated self-report questionnaire used to measure the severity of anxiety symptoms. Scores are calculated according to the instrument guidelines, with higher scores indicating greater anxiety severity. Change is calculated as the difference between pre-intervention and post-intervention scores.
Time frame: Baseline and immediately after completion of the 3-week intervention period
Change in Fibromyalgia Impact Score (Fibromyalgia Impact Questionnaire)
Fibromyalgia impact is assessed using the Fibromyalgia Impact Questionnaire, a validated instrument used to evaluate symptom severity, functional status, and overall impact of fibromyalgia on daily life. Scores are calculated according to the questionnaire instructions, with higher scores indicating greater disease impact. Change is calculated as the difference between pre-intervention and post-intervention scores.
Time frame: Baseline and immediately after completion of the 3-week intervention period
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