- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04890743
Effectiveness of Various Electrotherapy Methods in Treating People With Cervical Spine Pain Syndrome.
30. maj 2022 opdateret af: Jolanta Zwolińska, University of Rzeszow
Volunteers will take part in the study; Students of the university in the area of Rzeszow reporting chronic spinal ailments participation in remote learning.
Applicant participants will be randomised into 3 groups of subjected to various electrotherapy procedures.
Studieoversigt
Status
Rekruttering
Betingelser
Intervention / Behandling
- Andet: Kinesiotherapy combined with electrotherapy (Convenctional TENS method).
- Andet: Kinesiotherapy combined with electrotherapy (Pseudo-acupuncture TENS method).
- Andet: Kinesiotherapy combined with electrotherapy (Trabert ultrastimulation method)
- Andet: Kinesiotherapy combined with placebo electrotherapy
Detaljeret beskrivelse
Study participants will be tested:
- Before a series of electrotherapy treatments.
- 7 to 10 days after the end of electrotherapy.
3 months after the end of electrotherapy. The study will use
- a self-authored survey taking into account: basic personal data (age, gender, value and BMI, lifestyle and degree of load on the cervical spine), information on the nature, intensity and frequency of the presence of pain in the spine cervical system, taking into account possible adverse reactions
- a questionnaire for subcjective assessment of the state of the spine Neck Disability Index,
- measuring the tone of the vertebral muscles in the cervical (myotonometer),
- a visual analog scale used to assess the severity of symptoms (Visual Analog Scale -VAS) Intervention;
- irradiation of the neck area with a sollux lamp with a blue filter
- individual exercises conducted according to the prepared author's mobility improvement program
electrotherapy treatments:
- Trabert currents
- TENS currents (conventional)
- TENS currents (pseudo-acupuncture)
Undersøgelsestype
Interventionel
Tilmelding (Forventet)
60
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiekontakt
- Navn: Jolanta Zwolińska, PhD
- Telefonnummer: 505095199
- E-mail: jolantazwolinska@op.pl
Undersøgelse Kontakt Backup
- Navn: Paulina Sałaga
- Telefonnummer: 731275361
- E-mail: paulina.salaga@gmail.com
Studiesteder
-
-
Podkarpackie
-
Rzeszów, Podkarpackie, Polen, 35-310 Rzeszów
- Rekruttering
- Laboratorium Czynników Fizykalnych w Rehabilitacji w Przyrodniczo-Medycznym Centrum Badań Innowacyjnych Uniwersytetu Rzeszowskiego
-
Kontakt:
- Jolanta Zwolińska, PhD
- Telefonnummer: 505095199
- E-mail: jolantazwolinska@op.pl
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Kontakt:
- Lidia Perenc, prof.drhab.
- Telefonnummer: 722015220
- E-mail: lperenc@ur.edu.pl
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-
Deltagelseskriterier
Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.
Berettigelseskriterier
Aldre berettiget til at studere
19 år til 25 år (Voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- informed written consent of the patient to participate in the study
- no contraindications to electrotherapy in the area of the cervical spine;
Exclusion Criteria:
- poor tolerance of electrotherapy treatments;
- breaks between consecutive treatments longer than 3 days;
- failure to complete a series of kinesiotherapy and electrotherapy treatments;
- use of any stimulants during the observation period.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Conventional TENS group
One of the four groups created during randomization will undergo a unified program of kinesiotherapy and electrotherapy (Conventional TENS method).
|
One of the four groups created during randomization will undergo a unified program of kinesiotherapy and electrotherapy (Conventional TENS method).
|
|
Eksperimentel: Pseudo-acupuncture TENS group
One of the four groups created during randomization will undergo a unified program of kinesiotherapy and electrotherapy (Pseudo-acupuncture TENS method).
|
One of the four groups created during randomization will undergo a unified program of kinesiotherapy and electrotherapy (Pseudo-acupuncture TENS method).
|
|
Eksperimentel: Trabert ultrastimulation group
One of the four groups created during randomization will undergo a unified program of kinesiotherapy and electrotherapy (Trabert ultrastimulation method).
|
One of the four groups created during randomization will undergo a unified program of kinesiotherapy and electrotherapy (Trabert ultrastimulation method).
|
|
Placebo komparator: Placebo group
One of the four groups created during randomization will undergo a unified program of kinesiotherapy and placebo electrotherapy.
|
One of the four groups created during randomization will undergo a unified program of kinesiotherapy and placebo electrotherapy.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Neck Disability Index
Tidsramme: 1. Before a series of electrotherapy treatments.
|
A questionnaire for subcjective assessment of the state of the spine.
|
1. Before a series of electrotherapy treatments.
|
|
Neck Disability Index
Tidsramme: 2. 7 to 10 days after the end of electrotherapy.
|
A questionnaire for subcjective assessment of the state of the spine.
|
2. 7 to 10 days after the end of electrotherapy.
|
|
Neck Disability Index
Tidsramme: 3. 3 months after the end of electrotherapy.
|
A questionnaire for subcjective assessment of the state of the spine.
|
3. 3 months after the end of electrotherapy.
|
|
Myotonometer
Tidsramme: 1. Before a series of electrotherapy treatments.
|
Measuring the tone of the vertebral muscles in the cervical.
|
1. Before a series of electrotherapy treatments.
|
|
Myotonometer
Tidsramme: 2. 7 to 10 days after the end of electrotherapy.
|
Measuring the tone of the vertebral muscles in the cervical.
|
2. 7 to 10 days after the end of electrotherapy.
|
|
Myotonometer
Tidsramme: 3. 3 months after the end of electrotherapy.
|
Measuring the tone of the vertebral muscles in the cervical.
|
3. 3 months after the end of electrotherapy.
|
|
Visual Analog Scale
Tidsramme: 1. Before a series of electrotherapy treatments.
|
A Visual Analog Scale used to assess the severity of symptoms.
It enables the Patient to fine-tune the pain level on a scale from 0 to 10, where 0 is no pain at all and 10 is the maximum imaginable.
|
1. Before a series of electrotherapy treatments.
|
|
Visual Analog Scale
Tidsramme: 2. 7 to 10 days after the end of electrotherapy.
|
A Visual Analog Scale used to assess the severity of symptoms.
It enables the Patient to fine-tune the pain level on a scale from 0 to 10, where 0 is no pain at all and 10 is the maximum imaginable.
|
2. 7 to 10 days after the end of electrotherapy.
|
|
Visual Analog Scale
Tidsramme: 3. 3 months after the end of electrotherapy.
|
A Visual Analog Scale used to assess the severity of symptoms.
It enables the Patient to fine-tune the pain level on a scale from 0 to 10, where 0 is no pain at all and 10 is the maximum imaginable.
|
3. 3 months after the end of electrotherapy.
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Studieleder: Lidia Perenc, docent prof, University of Rzeszow
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
Generelle publikationer
- Cohen SP. Epidemiology, diagnosis, and treatment of neck pain. Mayo Clin Proc. 2015 Feb;90(2):284-99. doi: 10.1016/j.mayocp.2014.09.008.
- Martimbianco ALC, Porfirio GJ, Pacheco RL, Torloni MR, Riera R. Transcutaneous electrical nerve stimulation (TENS) for chronic neck pain. Cochrane Database Syst Rev. 2019 Dec 12;12(12):CD011927. doi: 10.1002/14651858.CD011927.pub2.
- Martins-de-Sousa PH, Guimaraes Almeida MQ, da Silva Junior JM, Santos AS, Costa Araujo GG, de Oliveira Pires F, Fidelis-de-Paula-Gomes CA, Koga Ferreira VT, Dibai-Filho AV. Program of therapeutic exercises associated with electrotherapy in patients with chronic neck pain: Protocol for a randomized controlled trial. J Bodyw Mov Ther. 2020 Jan;24(1):25-30. doi: 10.1016/j.jbmt.2019.04.008. Epub 2019 Apr 25.
Hjælpsomme links
- Review of clinical trials assessing the effectiveness of exercise therapy and electrotherapy.
- In the study included adults with chronic neck pain (lasting > 12 weeks) that compared TENS alone or in combination with other treatments versus active or inactive treatments. The primary outcomes were pain, disability and adverse events.
- The objective of this study will be to evaluate the clinical effects of adding high- and low-frequency transcutaneous electrical nerve stimulation (TENS) in a program of specific therapeutic exercises for the treatment of patients with chronic neck pain.
Datoer for undersøgelser
Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.
Studer store datoer
Studiestart (Faktiske)
1. april 2022
Primær færdiggørelse (Forventet)
30. november 2022
Studieafslutning (Forventet)
31. januar 2023
Datoer for studieregistrering
Først indsendt
29. april 2021
Først indsendt, der opfyldte QC-kriterier
17. maj 2021
Først opslået (Faktiske)
18. maj 2021
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
2. juni 2022
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
30. maj 2022
Sidst verificeret
1. oktober 2021
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- Urzeszow Club of Physical
Plan for individuelle deltagerdata (IPD)
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