An interventional study of GDS Muscle and Joint Chains Method and Conventional Physiotherapy in Adhesive Capsulitis and Frozen Shoulder, sponsored by Anahuac University. Completed at 1 site in Mexico. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-09-15.
Sponsored by Anahuac University · Not applicable, Interventional, and Treatment
This randomized exploratory clinical trial evaluated the effectiveness of the GDS Muscle and Joint Chains Method compared with conventional physiotherapy in patients with frozen shoulder (adhesive capsulitis). Thirty participants were randomly assigned to either the GDS intervention group or the conventional physiotherapy control group. Both interventions consisted of eight 50-minute sessions administered twice weekly for four weeks. The primary therapeutic objectives were to improve shoulder range of motion and reduce pain. Shoulder mobility was assessed using goniometry, and pain intensity was evaluated using a Visual Analog Scale. The study hypothesized that the GDS Muscle and Joint Chains Method would produce greater improvements in shoulder mobility and pain than conventional physiotherapy.
383 studies on the registry are indexed under Bursitis; 111 are open to participants now.
This study's enrollment of 30 is below the median of 44 across 346 interventional studies indexed under Bursitis.
Browse Bursitis studies →Anahuac University is the lead sponsor of 10 studies on the registry; 4 are open to participants now.
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Exclusion Criteria:
Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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Informed consent
Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.
You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
Contraindication
A reason a treatment, test or procedure should not be given to a particular person, such as an allergy, another illness or a medicine they take.
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Other: GDS Muscle and Joint Chains Method
Other: Conventional Physiotherapy
Participants received eight 50-minute sessions of the GDS Muscle and Joint Chains Method, administered twice weekly for four weeks. Treatment was individualized according to the participant's typology and included muscle reprogramming, postural and movement retraining, manual techniques applied along muscle-chain pathways, passive stretching, isometric and eccentric muscle activation, proprioceptive techniques, and strategies aimed at restoring balance between antagonistic and complementary muscle chains. Shoulder range of motion and pain intensity were assessed before and after the four-week intervention.
Participants received eight 50-minute conventional physiotherapy sessions administered twice weekly for four weeks. Treatment included application of a hot compress to the affected shoulder, 15 minutes of conventional transcutaneous electrical nerve stimulation (TENS) at 150 Hz with intensity adjusted to participant tolerance, 10 minutes of therapeutic ultrasound at 3 MHz and 0.8 W/cm² in pulsed mode at 50%, followed by 15 minutes of therapeutic exercise according to the MEDBRIDGE GO program. Shoulder range of motion and pain intensity were assessed before and after the intervention.
Change in Shoulder Range of Motion
Shoulder range of motion was measured in degrees using goniometry. Measurements included shoulder flexion, abduction, internal rotation, external rotation at 90° of abduction, and external rotation at 0°.
Time frame: Baseline and 4 weeks
Change in Pain Intensity
Pain intensity was assessed using a Visual Analog Scale ranging from 0 to 10, with 0 representing no pain and 10 representing the greatest pain intensity.
Time frame: Baseline and 4 weeks
Ran from Jan 2021 to primary completion in Aug 2023, 31 months.
Of 217 non-industry interventional studies with no phase under Bursitis, half reached primary completion within 10 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 17. This study's 31 months is above that.
Counting every sponsor, half of 217 studies reached it within 10 months; a quarter within 5 and three quarters within 17.
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This study is completed, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.
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Anahuac University