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NCT07150702
Effects of Close Follow-up on Patients With Low Back Pain
NA trial testing Conventional physical therapy program in Low Back Pain in 74 participants. Currently enrolling.
1 December 2025
Quick facts
| Lead sponsor | Istanbul Training and Research Hospital |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | treatment |
| Enrollment | 74 |
| Start date | 1 September 2025 |
| Primary completion | 1 December 2025 |
| Estimated completion | 10 December 2025 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Conventional physical therapy program
- Close follow-up by a physician
Conditions studied
- Low Back Pain — all drugs for Low Back Pain →
- Low Back Pain, Mechanical — all drugs for Low Back Pain, Mechanical →
Sponsor
Istanbul Training and Research Hospital
Who can join
Adults 18 to 65, any sex, with Low Back Pain or Low Back Pain, Mechanical. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This study will include patients aged 18-65 with subacute or chronic mechanical low back pain who apply to the Physical Medicine and Rehabilitation Clinic. The age, gender, body mass index, duration of low back pain, smoking status, and educational status of the patients included in the study will be recorded. Patients will be randomized into two groups: the study group and the control group. First, the psychosocial risk status of patients in both groups will be determined using the STarT Back Screening Tool. Then, patients in the control group will undergo a conventional physical therapy program that includes hot packs, transcutaneous electrical nerve stimulation, ultrasound, and core stabilization exercises. Patients in the study group will undergo daily close follow-up physician-patient meetings during the sessions, in addition to the conventional physical therapy program applied to the control group. Clinical assessments will be performed using the Visual Analogue Scale (VAS), Tampa Scale of Kinesiophobia, Pain Catastrophizing Scale, Beck's Depression Scale, Roland-Morris Disability Questionnaire, and Leeds Assessment of Neuropathic Symptoms and Signs. Clinical evaluations will be conducted at baseline, on Day 5 post-treatment, and at 1 month post-treatment.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07150702
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Currently open trials in the same condition.
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Other Istanbul Training and Research Hospital trials
Trials by the same sponsor.
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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 NCT07150702 (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 Istanbul Training and Research Hospital
- Last refreshed: 16 September 2025
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