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Reliability of Custom-Made Platform for Trunk Flexion Isometric Strength Assessment

16. juli 2026 opdateret af: Riphah International University

Reliability of Custom-Made Platform for Trunk Flexion Isometric Strength Assessment in Healthy Young Adults

Trunk flexion strength is an essential component of core muscle performance, playing a critical role in spinal stability, injury prevention, and athletic function. While isokinetic dynamometers remain gold standard for trunk strength assessment, their high cost and limited accessibility restrict their use in most clinical and field settings in Pakistan. There is a need for reliable, affordable alternative that can be used by physiotherapists and sports practitioners without access to specialized laboratory equipment. Therefore, this study aims to evaluate the reliability of a custom-made standing platform for measuring trunk flexion isometric strength in healthy young adults. Establishing the reliability of this device will enable clinicians and researchers to confidently use it as a practical and cost effective tool for trunk strength assessment in both clinical and sports settings.

Studieoversigt

Detaljeret beskrivelse

The custom-made platform is a standing device designed to measure maximal voluntary isometric trunk flexion force. During testing, participants stand on the platform and lean forward to a standardised angle of 17.5 degrees of trunk flexion. A trunk belt connected to a handheld dynamometer fixed to the rear platform records the force generated when the participant pushes forward against the belt during a maximal isometric contraction. Force is recorded in Newtons using Biopac Student Lab Pro software through the MP36 data acquisition unit.

A cross-sectional test-retest reliability design will be employed. Twenty-nine healthy male participants aged 18-25 years will be recruited from Riphah International University using non-probability convenience sampling. Each participant will attend two identical testing sessions spaced one week apart, conducted at the same time of the day to control for diurnal variation in muscle strength. During each session, participants will perform three maximal voluntary isometric trunk flexion contractions of five seconds duration, with sixty seconds of passive rest between trials. The average force across the three trials will be recorded in Newtons and used as the primary outcome variable for analysis.

Reliability will be assessed using the Intraclass Correlation Coefficients with two-way random effects model for absolute agreement, single measures - ICC (2,1) - reported alongside the 95% confidence interval. Values below 0.50 will be interpreted as poor reliability, 0.50 to 0.75 as moderate, 0.75 to 0.90 as good, and above 0.90 excellent. Absolute reliability will be quantified using the Standard Error of Measurement and the Minimal Detectable Change at 95% confidence level. Bland-Altman analysis will be used to assess systematic bias and limits of agreement between sessions. A paired t-test or Wilcoxon signed-rank test, depending on normality assessed by the Shapiro-Wilk test, will determine whether a statistically significant learning effect exists between Session 1 and Session 2. All statistical analyses will be conducted using SPSS Version 30 at a significance level of 0.05.

If the platform demonstrates good to excellent reliability, it will be validated as a feasible and affordable alternative to isokinetic dynamometry for trunk flexion isometric strength assessment, with direct implications for physiotherapy practice and sports science research in Pakistan.

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

29

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

      • Islamabad, Pakistan, 44000
        • Rekruttering
        • Riphah International University
        • Kontakt:
          • Farwa Abid, DPT

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

  • Voksen

Tager imod sunde frivillige

Ja

Beskrivelse

Inclusion Criteria:

  • Healthy males
  • Age between 18 and 25 years
  • Non-athletes
  • No history of musculoskeletal injuries specifically in the trunk region

Exclusion Criteria:

  • History of any medical condition that would affect trunk muscle strength
  • Athletes

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Andet
  • Tildeling: N/A
  • Interventionel model: Enkelt gruppeopgave
  • Maskning: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Andet: Reliability of Custom-Made Platform for Trunk Flexion Isometric Strength Assessment
Healthy adult participants will undergo repeated trunk flexion isometric strength assessments using a custom-made testing platform. Measurements will be repeated under standardized conditions by the same examiner to assess the reliability of the platform. No intervention will be administered.
Participants stand at 17.5° trunk flexion and perform 3 maximal isometric contractions of 5 seconds against a belt-connected dynamometer. Force recorded in Newtons. Repeated one week later.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Trunk muscles isometric strength
Tidsramme: 1 week.
Participants stand at 17.5° trunk flexion and perform 3 maximal isometric contractions of 5 seconds while attached to a dynamometer connected via a specalized harness. Force recorded in Newtons.
1 week.

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Saad Rauf, PhD, Riphah Interntional University, Isra University, Islamabad

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. maj 2026

Primær færdiggørelse (Anslået)

30. juli 2026

Studieafslutning (Anslået)

30. juli 2026

Datoer for studieregistrering

Først indsendt

16. juli 2026

Først indsendt, der opfyldte QC-kriterier

16. juli 2026

Først opslået (Faktiske)

21. juli 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

21. juli 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

16. juli 2026

Sidst verificeret

1. juli 2026

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • REC/MS-PT/02196 Farwa Abid

Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter

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