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NCT07174635: Tele-Nursing
The Effect of Tele-Nursing Service in Patients Diagnosed With Fibromyalgia
NA trial testing Intervention-telenursing in Pain in 44 participants. Completed in 14 June 2024.
14 June 2024
Quick facts
| Lead sponsor | Çankırı Karatekin University |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | triple |
| Primary purpose | prevention |
| Enrollment | 44 |
| Start date | 10 April 2024 |
| Primary completion | 14 June 2024 |
| Estimated completion | 14 June 2024 |
| Sites | 1 location across Turkey (Türkiye) |
Drugs / interventions tested
- Intervention-telenursing
Conditions studied
- Pain — all drugs for Pain →
- Tele-nursing — all drugs for Tele-nursing →
- Fibromyalgia Syndrome — all drugs for Fibromyalgia Syndrome →
Sponsor
Çankırı Karatekin University
Who can join
18 and older, any sex, with Pain or Tele-nursing. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The aim of the study was to determine the effect of tele-nursing service provided to patients diagnosed with fibromyalgia on the pain and activity level of patients. The study was designed as a randomised controlled experimental study in a pretest-posttest design. The research was conducted in a State Hospital between April 2024 and June 2024 with patients diagnosed with fibromyalgia who applied to the physical therapy outpatient clinic and met the inclusion criteria. The sample was divided into two groups as intervention and control groups of 22 participants by simple randomisation. Descriptive Information Form, Fibromyalgia Impact Questionnaire Revised (FIQR), Mcgill Pain Scale were used as data collection tools in the study. The second researcher was given the contact information of all patients and the data collection forms were applied as a pre-test. The second researcher did not know which group the patients were in. Thus, the researcher collecting the data was blinded. Data collection forms were administered by the researcher by interviewing the patient in approximately 15-20 minutes. Patients in the intervention group were called three times by phone and were trained in accordance with the prepared training booklet by first researcher.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT07174635
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
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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 NCT07174635 (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 Çankırı Karatekin University
- Last refreshed: 16 September 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/NCT07174635.
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