Last reviewed · How we verify
NCT06820073: GPR-KS_PI24/47
Effects of GPR with K-Stretch Hammock on Posture and Musculoskeletal Discomfort
NA trial testing Global Postural Reeducation (RPG) using the K-Stretch hammock in Cervical and Lumbar Musculoskeletal Discomfort in 32 participants. Currently enrolling.
20 April 2025
Quick facts
| Lead sponsor | Universidad San Jorge |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | crossover |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 32 |
| Start date | 1 February 2025 |
| Primary completion | 20 April 2025 |
| Estimated completion | 1 October 2025 |
| Sites | 1 location across Spain |
Drugs / interventions tested
- Global Postural Reeducation (RPG) using the K-Stretch hammock
Conditions studied
- Cervical and Lumbar Musculoskeletal Discomfort — all drugs for Cervical and Lumbar Musculoskeletal Discomfort →
Sponsor
Universidad San Jorge
Who can join
Adults 18 to 65, any sex, with Cervical and Lumbar Musculoskeletal Discomfort. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study aims to evaluate the effects of Global Postural Reeducation (RPG) using the K-Stretch hammock on workers at San Jorge University who experience neck and lower back discomfort due to prolonged sitting. The primary goal is to examine how this intervention impacts posture, musculoskeletal discomfort, flexibility, and range of motion, as well as participants' quality of life, stress levels, and sleep quality. Neck and lower back discomfort are common issues that significantly impact individuals' quality of life and work performance. Global Postural Reeducation (RPG) is a therapeutic approach that focuses on stretching and strengthening muscle chains to improve posture and alleviate discomfort. This study is innovative in applying RPG combined with a specialized K-Stretch hammock to assess its potential benefits in a workplace setting. Participants will include 32 administrative staff members aged 19 to 65 who work predominantly in seated positions and meet specific inclusion criteria. They will undergo a 6-week program involving bi-weekly 30-minute sessions. The study will also compare pre- and post-intervention results to evaluate changes in musculoskeletal discomfort, functional abilities, and physical alignment. Findings from this study may contribute to developing effective workplace interventions for musculoskeletal health.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06820073 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Universidad San Jorge
- Last refreshed: 11 February 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06820073.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing