Active Intervention for Patients With Neck Pain
29. august 2019 opdateret af: Marie Carmen Valenza, Universidad de Granada
Effects of an Active Program in Patients With Chronic Neck Pain: a Randomized Controlled Trial.
Neck pain is a complex biopsychosocial disorder often precipitated or aggravated by neck movements or sustained neck postures.
More than 80 % of individuals experience neck pain and neck associated disorders.
The aim of this study was to investigate the effects of a 4-week active exercising program in patients with chronic neck pain.
Studieoversigt
Detaljeret beskrivelse
While neck pain can be severely disabling and costly, treatment options have shown moderate evidence of effectiveness.
The optimal physiotherapy intervention is currently unclear.
Consequently, more research in this area combining different techniques in patients with a specific clinical profile is needed.
It has been previously shown that participants prefer self-care measures for the management of neck pain.
The aim of this study was to investigate the effects of a 4-week active exercising program in patients with chronic neck pain.
Undersøgelsestype
Interventionel
Tilmelding (Forventet)
50
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
-
Granada, Spanien, 18071
- Rekruttering
- Department of Physical Therapy
-
Kontakt:
- Marie Carmen Valenza, PhD
- E-mail: cvalenza@ugr.es
-
-
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
18 år til 65 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- To suffer from chronic neck pain (at least 3 months' duration)
- Neck pain of at least 3 on a visual analogue scale.
- Participants' symptoms should be at least partly related to increased nerve mechanosensitivity in the neck and upper limb confirmed by the reproduction of participants' symptoms by median nerve upper-limb neurodynamic test.
Exclusion Criteria:
- Whiplash related neck pain.
- Previous cervical surgical intervention.
- Cognitive impairments which prevent them to follow instructions.
- Visual or acoustic limitations.
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: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Active intervention
Patients will be included in an active intervention.
|
Patients allocated to the experimental group were included in an active exercising program adapted to each patient
|
|
Ingen indgriben: Control group
Patients in the control group will not receive any intervention
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Changes in number of active trigger points
Tidsramme: Changes from baseline to 4 weeks in the number of active trigger points assessed by palpation. The percentage of active trigger points is obtained.
|
Baseline, 4 weeks
|
Changes from baseline to 4 weeks in the number of active trigger points assessed by palpation. The percentage of active trigger points is obtained.
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Severity of pain
Tidsramme: Changes from baseline to 4 weeks in the severity of pain assessed using the Brief Pain Inventory. The severity and the interference of pain with daily life subscales were included. Score is the sum of the items divided by the number of items.
|
Baseline, 4 weeks
|
Changes from baseline to 4 weeks in the severity of pain assessed using the Brief Pain Inventory. The severity and the interference of pain with daily life subscales were included. Score is the sum of the items divided by the number of items.
|
|
Functionality
Tidsramme: Changes from baseline to 4 weeks on functionality assessed using the Neck Outcome Score.Symptoms, sleep disturbance, every day activity and pain and participation in everyday life subscales were included. They Ranged from 0 to 100 (no simptoms).
|
Baseline, 4 weeks
|
Changes from baseline to 4 weeks on functionality assessed using the Neck Outcome Score.Symptoms, sleep disturbance, every day activity and pain and participation in everyday life subscales were included. They Ranged from 0 to 100 (no simptoms).
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
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)
11. juni 2019
Primær færdiggørelse (Faktiske)
11. august 2019
Studieafslutning (Forventet)
11. september 2019
Datoer for studieregistrering
Først indsendt
11. juni 2019
Først indsendt, der opfyldte QC-kriterier
11. juni 2019
Først opslået (Faktiske)
17. juni 2019
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
4. september 2019
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
29. august 2019
Sidst verificeret
1. august 2019
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- DF0081UG
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .