- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT03501147
The Effect of a Resistance Training Program in Healthcare Workers on Pain, Workability and Physical Function.
The Effect of a Brief Daily Resistance Training Program in Healthcare Workers on Pain, Workability and Physical Function.
The prevalence and consequences of musculoskeletal pain is considerable among healthcare workers, allegedly due to high physical work demands of healthcare work.
Performing physical exercise at the workplace together with colleagues may be more motivating for some employees and thus increase adherence. On the other hand, physical exercise performed during working hours at the workplace may be costly for the employers in terms of time spend. Thus, it seems relevant to perform a brief intervention. This study is intended to investigate the difference between the effect of workplace-based physical exercise (using elastic bands and body weight exercises) and a group control on musculoskeletal pain, physical exertion during work, physical function, need for recovery, self-rated use of analgesics, and work ability among healthcare workers.
Studienübersicht
Status
Intervention / Behandlung
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
-
Valencia, Spanien, 46010
- Clinic Universitary Hospital of Valencia
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Healthcare Workers at the Hospital
- Informed consent
Exclusion Criteria:
- Unable to perform exercises
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Verhütung
- Zuteilung: Nicht randomisiert
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Single
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
---|---|
Experimental: Intervention
15 minutes of resistance training at the work place every day
|
15 minutes of resistance training during work every day
|
Kein Eingriff: Control
Usual work
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Pain overall status: Standard 7-point patient global impression
Zeitfenster: 2 days after the end of intervention (POST)
|
Standard 7-point patient global impression of pain collected at the endpoint
|
2 days after the end of intervention (POST)
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
---|---|---|
Workability Index
Zeitfenster: Baseline
|
Questionnaire work ability
|
Baseline
|
Workability Index
Zeitfenster: 2 days after the end of intervention (POST)
|
Questionnaire work ability
|
2 days after the end of intervention (POST)
|
Physical function
Zeitfenster: Baseline
|
Physical tests (push-ups, Biering-Sorensen test, Sit to Stand)
|
Baseline
|
Physical function
Zeitfenster: 2 days after the end of intervention (POST)
|
Physical tests (push-ups, Biering-Sorensen test, Sit to Stand)
|
2 days after the end of intervention (POST)
|
Perceived physical exertion
Zeitfenster: Baseline
|
Based on Borg's rate of perceived exertion (RPE) (Borg CR10 scale)
|
Baseline
|
Perceived physical exertion
Zeitfenster: 3 weeks of resistance training
|
Based on Borg's rate of perceived exertion (RPE) (Borg CR10 scale)
|
3 weeks of resistance training
|
Perceived physical exertion
Zeitfenster: 6 weeks of resistance training
|
Based on Borg's rate of perceived exertion (RPE) (Borg CR10 scale)
|
6 weeks of resistance training
|
Perceived physical exertion
Zeitfenster: 2 days after the end of intervention (POST)
|
Based on Borg's rate of perceived exertion (RPE) (Borg CR10 scale)
|
2 days after the end of intervention (POST)
|
"Need for recovery scale" after work
Zeitfenster: Baseline
|
Five point scale (1 = never, 5 = always)
|
Baseline
|
"Need for recovery scale" after work
Zeitfenster: 3 weeks of resistance training
|
Five point scale (1 = never, 5 = always)
|
3 weeks of resistance training
|
"Need for recovery scale" after work
Zeitfenster: 6 weeks of resistance training
|
Five point scale (1 = never, 5 = always)
|
6 weeks of resistance training
|
"Need for recovery scale" after work
Zeitfenster: 2 days after the end of intervention (POST)
|
Five point scale (1 = never, 5 = always)
|
2 days after the end of intervention (POST)
|
Self-rated use of analgesics
Zeitfenster: Baseline
|
The number of days the participants used analgesics during the last week
|
Baseline
|
Self-rated use of analgesics
Zeitfenster: 3 weeks of resistance training
|
The number of days the participants used analgesics during the last week
|
3 weeks of resistance training
|
Self-rated use of analgesics
Zeitfenster: 6 weeks of resistance training
|
The number of days the participants used analgesics during the last week
|
6 weeks of resistance training
|
Self-rated use of analgesics
Zeitfenster: 2 days after the end of intervention (POST)
|
The number of days the participants used analgesics during the last week
|
2 days after the end of intervention (POST)
|
Pain: Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10)
Zeitfenster: Baseline
|
Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10, 0 = not pain, 10 = worst possible pain)
|
Baseline
|
Pain: Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10)
Zeitfenster: 3 weeks of resistance training
|
Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10, 0 = not pain, 10 = worst possible pain)
|
3 weeks of resistance training
|
Pain: Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10)
Zeitfenster: 6 weeks of resistance training
|
Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10, 0 = not pain, 10 = worst possible pain)
|
6 weeks of resistance training
|
Pain: Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10)
Zeitfenster: 2 days after the end of intervention (POST)
|
Average pain intensity (Visual Analogue Scale (VAS) Scale 0-10, 0 = not pain, 10 = worst possible pain)
|
2 days after the end of intervention (POST)
|
Mitarbeiter und Ermittler
Sponsor
Ermittler
- Studienstuhl: Jose C Granell, PhD, University of Valencia
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 0000260894
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
Klinische Studien zur Muskel-Skelett-Schmerzen
-
Foundation IRCCS San Matteo HospitalAktiv, nicht rekrutierendGreater Trochanteric Pain Syndrome beider unteren ExtremitätenItalien
-
Gazi UniversityAbgeschlossenGesäß-Tendinitis | Greater Trochanteric Pain Syndrome beider unteren ExtremitätenTruthahn
-
Lawson Health Research InstituteNoch keine RekrutierungSchmerzen im unteren Rücken | Greater Trochanteric Pain Syndrome
-
C.R.Darnall Army Medical CenterUnbekanntGreater Trochanteric Pain SyndromeVereinigte Staaten
-
Guna S.p.aBeendetGreater Trochanteric Pain Syndrome | Pertrochantäre Fraktur | Gesäß-Tendinitis | GTPS - Greater Trochanteric Pain Syndrome | Sehnenerkrankung | GesäßmuskulaturItalien
-
NHS Greater Glasgow and ClydeNHS Research ScotlandRekrutierungGreater Trochanteric Pain SyndromeVereinigtes Königreich
-
Smith & Nephew, Inc.AbgeschlossenHüftschmerzen chronisch | Greater Trochanteric Pain SyndromeAustralien
-
Kutahya Health Sciences UniversityRekrutierungGreater Trochanteric Pain SyndromeTruthahn
-
Massachusetts General HospitalAbgeschlossenGreater Trochanteric Pain SyndromeVereinigte Staaten
-
Montefiore Medical CenterNoch keine RekrutierungGreater Trochanteric Pain SyndromeVereinigte Staaten
Klinische Studien zur Resistance training
-
University of California, San DiegoAbgeschlossenAutismus-Spektrum-Störung | Autistische StörungVereinigte Staaten
-
San Diego State UniversityUniversity of California, San DiegoAbgeschlossen
-
Umeå UniversityKarlstad UniversityRekrutierungParkinson Krankheit | Kognitive BeeinträchtigungSchweden
-
Maastricht University Medical CenterBeendetÜberfütterung und BewegungNiederlande
-
Taichung Veterans General HospitalAbgeschlossen
-
Karolinska InstitutetRegion Stockholm; Stiftelsen Sunnerdahls Handikappfond; Swedish Foundation for... und andere MitarbeiterAbgeschlossenAufmerksamkeitsdefizitsyndromSchweden
-
KTO Karatay UniversityAbgeschlossenStreicheln | Schlaganfall-RehabilitationTruthahn
-
Chiang Mai UniversityAbgeschlossenLeichte kognitive EinschränkungThailand
-
VA Office of Research and DevelopmentAbgeschlossenParkinson-Krankheit | Leichte kognitive EinschränkungVereinigte Staaten
-
Chang Gung UniversityAbgeschlossenGesunde ältere ErwachseneTaiwan