The goal of this clinical trial is to learn whether adding breathing training to an exercise program can improve pain, mood, and thinking skills in adults with chronic spinal pain. The main questions it aims to answer are: * Does adding breathing training lower pain and its impact on daily life? * Does it improve symptoms of anxiety and depression? * Does it improve thinking skills, such as attention and mental flexibility? Researchers will compare three groups to see if adding breathing training provides additional benefits: * a group that performs exercise only * a group that performs exercise combined with breathing training * a group that receives general advice only Participants will: * take part in a 12-week program * attend one supervised session each week * complete two home-based (unsupervised) exercise sessions each week (about 30 minutes each) Participants in the combined group will also: * learn breathing techniques during supervised sessions using biofeedback (a method that provides real-time feedback on breathing patterns) * practice breathing exercises at home four times per week (about 10 minutes each) without biofeedback support
This study examined the effects of a structured exercise program, with or without diaphragmatic breathing training, in adults with chronic non-specific musculoskeletal pain of the spine. Chronic pain was defined as pain persisting for at least 12 weeks or recurring over a prolonged period. Non-specific musculoskeletal pain refers to pain that cannot be attributed to a specific underlying pathology, such as fracture, trauma, or systemic disease, and is not associated with conditions that require surgical treatment. Participants were recruited from the general population through an open call distributed across academic, clinical, and occupational settings. Individuals who expressed interest were screened for eligibility according to predefined criteria. Eligible participants were randomly assigned to one of three groups: an exercise-only group, a combined exercise and diaphragmatic breathing group, or a minimal intervention control group. All participants in the intervention groups followed a 12-week program that included supervised and home-based sessions. The exercise program was designed to improve spinal mobility, functional movement, flexibility, and neuromuscular control through progressive, multi-planar exercises performed in seated and standing positions. The combined intervention group additionally received training in diaphragmatic breathing supported by biofeedback during supervised sessions and practiced breathing exercises independently at home. The control group received psychoeducation and general recommendations for physical activity, including walking, stretching, and relaxation techniques. Validated clinical, psychological, and neuropsychological measures were used to assess pain, emotional status, quality of life, cognitive performance, and behavioral responses. These measures were administered at baseline, after completion of the intervention, and at follow-up. All procedures were conducted according to predefined protocols to ensure consistency across groups.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
183
A structured exercise program targeting spinal mobility, muscular strengthening, postural control, flexibility, and neuromuscular coordination. Exercises were performed in seated and standing positions and included multi-planar functional movements, stretching, and mobilization of joints and neural tissue. The program was delivered over 12 weeks with one supervised session per week and additional unsupervised home-based sessions.
A biofeedback-assisted breathing intervention involving slow, controlled diaphragmatic breathing with emphasis on nasal inhalation and prolonged exhalation. Breathing was guided by visual pacing to regulate rhythm and promote a target breathing rate. Training was delivered during supervised sessions and practiced independently at home throughout the intervention period.
Private Practice
Heraklion, Crete, Greece
Democritus University of Thrace, Department of Physical Education and Sport Science
Komotini, Thrace, Greece
Pain intensity and pain-related interference
Pain intensity and interference were assessed using the Brief Pain Inventory - Short Form (BPI-SF). Pain severity and interference scores range from 0 to 10, with higher scores indicating greater pain and functional impact.
Time frame: Baseline, post-intervention (12 weeks), and 4-week follow-up
Emotional status (anxiety and depression)
Emotional status was assessed using the Hospital Anxiety and Depression Scale (HADS), a 14-item instrument with two subscales (anxiety and depression), each item scored from 0 to 3, with higher scores indicating greater symptom severity.
Time frame: Baseline, post-intervention (12 weeks), and 4-week follow-up
Cognitive flexibility
Cognitive flexibility was assessed using the Trail Making Test (Part A and Part B) and the Stroop Color-Word Test. Performance was evaluated based on completion time and interference indices, with higher completion times and greater interference indicating lower cognitive flexibility.
Time frame: Baseline, post-intervention (12 weeks), and 4-week follow-up
Adherence to the intervention
Adherence was defined as the total time (in minutes) of home-based (unsupervised) practice, recorded prospectively by participants throughout the intervention period using standardized weekly logs. Participants documented the frequency, type, and duration of exercise and, where applicable, diaphragmatic breathing practice.
Time frame: Throughout the 12-week intervention period
Quality of life (WHOQOL-BREF total and domain scores)
Quality of life was assessed using the World Health Organization Quality of Life - BREF (WHOQOL-BREF), a 26-item instrument measuring physical, psychological, social, and environmental domains. Items are rated on a 5-point Likert scale, with higher scores indicating better perceived quality of life.
Time frame: Baseline, post-intervention (12 weeks), and 4-week follow-up
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