Effects of Health Education for Patients Received Minimally Invasive Lumbar Spinal Surgery
7. oktober 2019 oppdatert av: Taipei Medical University Shuang Ho Hospital
Lumbar degenerative disease surgery has been a routine clinical operation, and has good treatment effects.
Although the patient's neurological symptoms improve after surgery, many patients still have postoperative muscle soreness.
The postoperative rehabilitation intervention for the patients receiving traditional lumbar surgery has been confirmed to effectively improve pain and disability.
However, in recent years, minimally invasive lumbar spinal surgery has gradually replaced traditional surgery, postoperative pain has been greatly reduced.
Therefore, patients have the opportunity to receive early intervention in rehabilitation, but there is no standardization process for rehabilitation of minimally invasive lumbar spine surgery.
Therefore, this study aims to establish a health education program for patients receiving minimally invasive lumbar spinal surgery, and conduct clinical trials to test its effectiveness.
Studieoversikt
Status
Ukjent
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Forventet)
100
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Taipei, Taiwan, 235
- Rekruttering
- Taipei Medical University-Shuang Ho Hospital
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Ta kontakt med:
- Chiao-Ling Chen, Master
- Telefonnummer: 8127 886-02-22490088
- E-post: 18395@s.tmu.edu.tw
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Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
45 år til 90 år (Voksen, Eldre voksen)
Tar imot friske frivillige
Nei
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- Age between 45 and 90 years old.
- Low back pain has been persisting at least 3 months.
- Clinical degeneration diagnosis supports the need of MI-TLIF.
- Able to understand Chinese.
Exclusion Criteria:
- Emergency surgery.
- Unstable vital sign.
- Any psychological, neurological, orthopedics, cardiopulmonary, and cancer history.
- Had spinal surgery before.
- Pregnancy.
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
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Ingen inngripen: Vanlig omsorgsgruppe
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Eksperimentell: Utdanningsgruppe
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Physical therapist will be consulted one day before and after the operation (OP) day.
On the day before the OP day, they focus on education, including how to get up from bed and stand up from a chair.
Five rehabilitation exercises are also demonstrated: 1) ankle flexion and extension, 2) knee flexion and extension, 3) hip joint abduction and adduction, 4) hip joint flexion and extension, and 5) drawing-in maneuver.
The participants will be required to repeat each component to confirm that they can do it correctly.
Each exercise is suggested to be done 10 times per day following MI-TLIF, and the number will be recorded 3 days (pre-OP day, post-OP day, and post-OP day 2).
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Change of Oswestry Disability Index
Tidsramme: The day before operation day, and 1, 3, 6 months after surgery
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This scale evaluates subject's physical function.
The range is 0 to 1. Higher values represent a better outcome.
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The day before operation day, and 1, 3, 6 months after surgery
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Change of Visual Analogue Scale
Tidsramme: The day before operation day, and 1, 3, 6 months after surgery
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This scale evaluates subject's pain intensity.
"0" indicates no pain and "10" indicates the worst possible pain.
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The day before operation day, and 1, 3, 6 months after surgery
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Change of Short Form 12 version 2
Tidsramme: The day before operation day, and 1, 3, 6 months after surgery
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This scale evaluates subject's health-related quality of life.
We will record the subscales: physical component summary (PCS) and mental component summary (MCS).
Higher values represent a better outcome.
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The day before operation day, and 1, 3, 6 months after surgery
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Change of Functional reach test
Tidsramme: The day before operation day, and 1, 3, 6 months after surgery
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It is a dynamic measure of balance.
A 100 cm yardstick will be horizontally set on the wall with the acromion height.
The patient will be asked to make a fit and reach forward as far as possible without moving his/her feet.
It will be measured twice and the better outcome will be recorded.
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The day before operation day, and 1, 3, 6 months after surgery
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Change of 30-second Chair Rise
Tidsramme: The day before operation day, and 1, 3, 6 months after surgery
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It is used to evaluate the lower limb function and strength relating to the daily activities.
The patient starts with a sitting position, and need to repeat stand-to-sit movements.
He/She will be encouraged to move safely as soon as possible in 30 minutes.
Higher number indicates better function.
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The day before operation day, and 1, 3, 6 months after surgery
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Change of Timed Up and Go test
Tidsramme: The day before operation day, and 1, 3, 6 months after surgery
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It was developed to measure subjects' balance and mobility.
The patient starts with a sitting position, stands up, walks a 3-meter distance, turns, walks back, and sits down.
He/She will be encouraged to finish it safely as soon as possible.
A shorter time indicates better function.
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The day before operation day, and 1, 3, 6 months after surgery
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Change of 15-m walk test
Tidsramme: The day before operation day, and 1, 3, 6 months after surgery
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Gait speed shows good reliability and is valid to assess physical mobility.
A 15-mile straight line will be mounted on a flat surface.
The patient will be required to walk down the line at the maximal speed.
He/She will be encouraged to finish it safely as soon as possible.
A shorter time indicates better function.
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The day before operation day, and 1, 3, 6 months after surgery
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
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Length of hospitalization
Tidsramme: The duration between admission and discharge
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The duration between admission and discharge
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Narcotic use during hospitalization
Tidsramme: The duration between admission and discharge
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The duration between admission and discharge
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Return-to-work status
Tidsramme: up to 6 months after surgery
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up to 6 months after surgery
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Adverse events
Tidsramme: up to 6 months after surgery
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The rate of infection and the rate of re-operation (including: dural tear, cage migration and retropulsion, and screw loosening).
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up to 6 months after surgery
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Etterforskere
- Studiestol: Heng-Wei Liu, Doctor, Shuangho Hospital
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart (Faktiske)
25. april 2019
Primær fullføring (Forventet)
1. oktober 2021
Studiet fullført (Forventet)
1. januar 2022
Datoer for studieregistrering
Først innsendt
6. oktober 2019
Først innsendt som oppfylte QC-kriteriene
7. oktober 2019
Først lagt ut (Faktiske)
9. oktober 2019
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
9. oktober 2019
Siste oppdatering sendt inn som oppfylte QC-kriteriene
7. oktober 2019
Sist bekreftet
1. oktober 2019
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- N201904001
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