Sacroiliac Manipulation and Core Stability in Healthy Adults

NCT ID: NCT07244679

Last Updated: 2025-11-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-03-30

Study Completion Date

2022-06-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Sacroiliac joint (SIJ) dysfunction is a common cause of lumbopelvic instability, often linked to altered load transfer between the spine and lower limbs. Although various therapeutic interventions are used to restore joint alignment and improve neuromuscular control, the immediate effects of chiropractic manipulation on core stabilization in asymptomatic individuals remain unclear. This randomized controlled study aimed to examine the acute impact of bilateral sacroiliac joint high-velocity, low-amplitude (HVLA) manipulation on trunk stability in healthy adults. Sixty participants aged 18-40 years were randomly assigned to either a manipulation group or a control group. Core stabilization performance and postural control were evaluated using standardized tests including the Centaur Trunk Training (CTT) biofeedback system, plank, sit-ups endurance, and flexibility assessments. The findings demonstrated significant short-term improvements in trunk stability and flexibility following manipulation, suggesting that sacroiliac joint adjustments may positively influence neuromuscular activation and motor control in healthy individuals.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

SIJ is recognized as a key anatomical structure responsible for transmitting mechanical loads between the spine and the lower extremities. Even minor restrictions in SIJ mobility have the potential to alter lumbopelvic alignment, modify core muscle activation patterns, and influence postural stability. Although these alterations may occur in symptomatic and asymptomatic populations alike, the precise neuromuscular mechanisms through which SIJ mobility affects trunk control remain an area of ongoing scientific inquiry.

Manual therapy techniques-particularly HVLA manipulation-are frequently employed to restore joint mobility, regulate proprioceptive input, and optimize neuromuscular coordination within the lumbopelvic region. HVLA manipulation has been proposed to facilitate rapid mechanical and neurophysiological responses, including improved segmental motion, enhanced afferent feedback, and short-term modifications in motor unit recruitment. Despite these proposed mechanisms, empirical evidence concerning the acute effects of SIJ-directed HVLA manipulation in healthy adults is limited.

Core stabilization constitutes another critical component of lumbopelvic rehabilitation. This approach emphasizes the activation, endurance, and coordinated function of deep trunk musculature-particularly the transversus abdominis, multifidus, and associated stabilizer groups-which collectively contribute to spinal alignment and postural equilibrium. Core stabilization strategies are widely supported in theory; however, their interaction with manual therapy techniques, especially in terms of immediate biomechanical and neuromuscular responses, has not been thoroughly examined in healthy individuals.

This randomized controlled trial was designed to investigate the immediate effects of bilateral SIJ HVLA manipulation on trunk stability and postural control in healthy adults. The study was conducted at Ataşehir Florence Nightingale Hospital and included participants aged 18-40 years who met predefined eligibility criteria. After completing baseline assessments, participants were randomly assigned to one of two groups:(1) the SIJ Manipulation Group, which received bilateral HVLA manipulation at the posterior superior iliac spines (PSIS) in a side-lying position, and (2) the Control Group (No Treatment), which completed the same assessment procedures without receiving any therapeutic intervention.

A comprehensive set of outcome measures was selected to evaluate multiple dimensions of lumbopelvic function. Pelvic alignment patterns were examined using the Derifield-Thompson leg check, while lumbar spine mobility was assessed with the Modified Schober Test. Core endurance and trunk muscle performance were measured using standardized sit-up and plank tests. The most detailed assessment was performed with the CTT biofeedback system, an objective device capable of analyzing postural control across 22 angular positions ranging from 0° to ±180°, thereby providing multidimensional insight into trunk stability.

The HVLA manipulation procedure involved a brief, controlled thrust delivered bilaterally to the SIJ region following established clinical guidelines. All post-intervention assessments were performed immediately after the procedure according to the predefined protocol. Ethical approval for the study was obtained from the Istanbul Yeni Yüzyıl University Clinical Research Ethics Committee (Decision No: 24.03.2022/14), and written informed consent was obtained from all participants prior to enrollment.

This trial was designed to explore the theoretical mechanisms through which SIJ manipulation may influence trunk stability, neuromuscular activation, and early postural adjustments in asymptomatic individuals. The findings and statistical outcomes of the study will be reported separately in the Results section of this clinical trial record. The present protocol description is intended solely to outline the scientific rationale, methodological framework, and procedural details of the study, without including any data-driven conclusions.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Health Adults Core Stabilization

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

a randomized, controlled, single-blind, prospective study
Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Outcome Assessors
Randomization will be done by sealed envelope method

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

SIJ Manipulation Group

Bilateral HVLA SIJ manipulation applied at PSIS

Group Type EXPERIMENTAL

Sacroiliac Joint Manipulation (HVLA)

Intervention Type OTHER

HVLA manipulation applied bilaterally at the sacroiliac joint (PSIS) to improve lumbopelvic stability.

Control Group (No Treatment)

Participants received no manipulation; only baseline and post-test evaluations were performed.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Sacroiliac Joint Manipulation (HVLA)

HVLA manipulation applied bilaterally at the sacroiliac joint (PSIS) to improve lumbopelvic stability.

Intervention Type OTHER

Other Intervention Names

Discover alternative or legacy names that may be used to describe the listed interventions across different sources.

Experimental Group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Healthy adults aged between 18 and 40 years
* No history of low back or pelvic pain within the last 6 months
* No previous spinal or sacroiliac joint surgery
* No current neurological or musculoskeletal disorders
* Able to maintain standing and sitting positions without discomfort
* Voluntary participation with informed consent

Exclusion Criteria

* History of chronic low back pain or sacroiliac dysfunction
* Previous fractures, dislocations, or surgery in the lumbopelvic region
* Neurological, vestibular, or systemic disorders affecting balance or movement
* Pregnancy or suspected pregnancy
* Use of pain medication, muscle relaxants, or anti-inflammatory drugs within the last 48 hours
* Contraindications to manual therapy (osteoporosis, malignancy, inflammatory joint disease, acute disc herniation, cauda equina syndrome)
* Refusal or inability to participate in the study protocol
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Bahçeşehir University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Esra BECENI

Lecturer

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Ataşehir Florence Nightingale Hospital

Istanbul, , Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

BAU-FTR-SIJCORE-2022

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.