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Hamstring Tightness and Lumbar Lordosis Angel Across Functional Sitting Posture. (LLA-HT)

2. Juli 2026 aktualisiert von: Ahmed youssef saleh saeed, Cairo University

Correlation Between Hamstring Tightness and Lumbar Lordosis Angel Across Functional Sitting Posture in Sedentary Adults.

The goal of this observational study is to learn about the relationship between hamstring tightness and the lumbar lordosis angle in sedentary adults across different sitting postures. The main question it aims to answer is:

Is hamstring tightness related to the lumbar lordosis angle across three functional sitting postures (upright, slumped, and forward-leaning)? It also asks whether hamstring tightness differs between men and women, whether it differs between the dominant and non-dominant leg, and whether the lumbar lordosis angle differs between men and women across the three postures.

Participants will have their hamstring tightness measured with the Active Knee Extension test and their lumbar lordosis angle measured with a bubble inclinometer while sitting in each of the three postures.

Studienübersicht

Detaillierte Beschreibung

Prolonged sitting is a defining feature of contemporary sedentary lifestyles and an established risk factor for musculoskeletal disorders of the lumbar spine. During sustained sitting, the hip is held in flexion and the hamstring muscle-tendon unit is maintained in a shortened position, which over time is associated with reduced hamstring extensibility (hamstring tightness). Because the hamstrings originate from the ischial tuberosity, a loss of hamstring extensibility exerts a posteriorly directed pull on the pelvis, promoting posterior pelvic tilt. Through regional spinopelvic coupling, this change in pelvic orientation alters the sacral slope and, consequently, the lumbar lordosis angle.

Although the relationship between hamstring tightness and lumbar lordosis has been described previously, most existing studies have evaluated it in the standing position. Sedentary individuals, however, spend the majority of their day seated, where the line of gravity, baseline muscle activity, and passive tissue demands placed on the spine differ substantially from those in standing. Evidence is therefore limited regarding how hamstring tightness relates to the lumbar lordosis angle across the functional sitting postures encountered in daily life, and regarding how this relationship may vary by sex and between the dominant and non-dominant lower limb.

This cross-sectional observational study will be conducted on 110 sedentary adults (55 male and 55 female), aged 18 to 45 years, recruited according to predefined eligibility criteria. The sample size was determined using G*Power based on a bivariate-normal correlation model. Eligible participants will be sedentary (more than six hours of sitting per day and a physical-activity level below 600 MET-minutes/week on the International Physical Activity Questionnaire), with a body mass index below 30 kg/m², bilateral hamstring tightness, and no current low back pain or other exclusionary conditions.

Following screening and informed consent, each participant's demographic and anthropometric data will be recorded, and lower-limb dominance will be determined using a three-task behavioral battery. Hamstring tightness will be assessed bilaterally using the Active Knee Extension (AKE) test, recorded with a digital goniometer, with the mean of three trials used for analysis. The lumbar lordosis angle (T12-S2) will be measured using a double bubble inclinometer in three randomized functional sitting postures-upright, slumped, and forward-leaning-with the mean of three trials per posture used for analysis.

The primary aim is to examine the correlation between hamstring tightness and the lumbar lordosis angle in each of the three sitting postures. The secondary aims are to compare hamstring tightness between male and female participants, to compare hamstring tightness between the dominant and non-dominant lower limb, and to compare the lumbar lordosis angle between male and female participants across the three postures. Data will be analyzed using Pearson correlation coefficients, independent- and paired-samples t-tests, and a mixed-design analysis of variance, with the significance level set at p < 0.05.

Studientyp

Beobachtungs

Einschreibung (Geschätzt)

110

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

    • Shubra Misr
      • Cairo, Shubra Misr, Ägypten, 12616

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

  • Erwachsene

Akzeptiert gesunde Freiwillige

Ja

Probenahmeverfahren

Nicht-Wahrscheinlichkeitsprobe

Studienpopulation

Sedentary adults of both sexes, aged 18 to 45 years, recruited from the Nasser institute hospital, and the surrounding community. Eligible participants are healthy individuals with a sedentary lifestyle (more than six hours of sitting per day and a physical-activity level below 600 MET-minutes per week on the International Physical Activity Questionnaire), a body mass index below 30 kg/m², and bilateral hamstring tightness, with no current low back pain or other excluding musculoskeletal, neurological, or spinal conditions

Beschreibung

Inclusion Criteria:

  • Healthy adults aged 18-45 years.
  • Sedentary occupation requiring > 6 hours of sitting per day.
  • Active Knee Extension (AKE) angle >15°.
  • Bilateral hamstring tightness.
  • Sedentary individual as determined by IPAQ (MET≤ 600 min/week).
  • Asymptomatic for low back pain at the time of testing.

Exclusion Criteria:

  • History of significant low back pain requiring medical treatment in the past 12 months.
  • Previous spinal surgery or structural spinal deformities.
  • Lower extremity injury or surgery within the past 6 months.
  • Neurological disorders affecting sensation or movement.
  • Pregnant female or get birth in the last year.
  • Body mass index (BMI) ≥ 30 kg/m².
  • postural deviations resulting from shortening of the iliopsoas and erector spinae or insufficiency of the core stabilizers and hip extensors

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

Kohorten und Interventionen

Gruppe / Kohorte
Intervention / Behandlung
Sedentary adults
Sedentary adults aged 18-45 years (55 male, 55 female) with bilateral hamstring tightness and no current low back pain, assessed for hamstring tightness (Active Knee Extension test) and lumbar lordosis angle (bubble inclinometer) across three functional sitting postures (upright, slumped, and forward-leaning).
Hamstring tightness measured bilaterally with the Active Knee Extension test (digital goniometer) and lumbar lordosis angle (T12-S2) measured with a bubble inclinometer across three functional sitting postures. No therapeutic intervention is administered; these are observational measurements only.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Correlation between hamstring tightness and lumbar lordosis angle across three functional sitting postures
Zeitfenster: At a single assessment session (cross-sectional; Day 1).
Hamstring tightness is measured as the Active Knee Extension (AKE) deficit in degrees (mean of three trials per limb, using a digital goniometer). The lumbar lordosis angle is measured in degrees using a bubble inclinometer (T12-S2, mean of three trials per posture) in three functional sitting postures: upright, slumped, and forward-leaning. The association between hamstring tightness and the lumbar lordosis angle is assessed for each posture using the Pearson correlation coefficient.
At a single assessment session (cross-sectional; Day 1).

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Difference in hamstring tightness between males and females
Zeitfenster: At a single assessment session (cross-sectional; Day 1).
Hamstring tightness (bilateral mean Active Knee Extension deficit, in degrees) compared between male and female participants.
At a single assessment session (cross-sectional; Day 1).
Difference in hamstring tightness between the dominant and non-dominant lower limb
Zeitfenster: At a single assessment session (cross-sectional; Day 1).
Hamstring tightness (Active Knee Extension deficit, in degrees) compared between the dominant and non-dominant limb. Limb dominance is determined using a three-task behavioral battery.
At a single assessment session (cross-sectional; Day 1).
Difference in lumbar lordosis angle between males and females across the three sitting postures
Zeitfenster: At a single assessment session (cross-sectional; Day 1).
Lumbar lordosis angle (degrees, bubble inclinometer, T12-S2) compared between male and female participants in each of the three functional sitting postures (upright, slumped, forward-leaning).
At a single assessment session (cross-sectional; Day 1).

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. August 2026

Primärer Abschluss (Geschätzt)

1. Oktober 2026

Studienabschluss (Geschätzt)

1. Dezember 2026

Studienanmeldedaten

Zuerst eingereicht

27. Juni 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

27. Juni 2026

Zuerst gepostet (Tatsächlich)

2. Juli 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

6. Juli 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

2. Juli 2026

Zuletzt verifiziert

1. Juli 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Plan für individuelle Teilnehmerdaten (IPD)

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NEIN

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Ja

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