Does Spinal Manipulation Therapy Impact Lumbar Proprioception

Sponsor
Balgrist University Hospital (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04869514
Collaborator
(none)
150
4
32

Study Details

Study Description

Brief Summary

Background: One mechanism underlying the clinical effects of spinal manipulation therapy (SMT) might be related to sustained changes in the signaling of proprioceptive afferents, thereby affecting proprioceptive function. Proprioceptive function can be assessed using vibrotactile stimulation (VS) in combination with balance control. The central nervous system uses different proprioceptive weighting (PW) strategies by modifying the weighting of proprioceptive signals from either ankle or paraspinal muscles, depending on environmental changes. For example, during VS, healthy participants at risk of developing back pain have demonstrated increased reliance on ankle instead of lumbar proprioception. Therefore, a potential effect of SMT on lumbar proprioceptive function can be tested by comparing pre- and post-SMT PW strategies by using VS and balance control. Objectives: The investigators aim to compare changes in PW strategies in healthy participants after lumbar and thoracic SMT, lumbar mobilization and no intervention.

Methods: Using a randomized controlled trial, participants will undergo two visits within 10 days, receiving the intervention in the first visit and pre- and post-intervention postural sway assessments. Primary outcomes will include changes of postural sway and PW ratios. Data will be analyzed by linear mixed models.

Condition or Disease Intervention/Treatment Phase
  • Procedure: spinal manipulation
N/A

Detailed Description

Manual therapy is widely used by patients with back pain with about 75% of patients consulting either a chiropractor, physiotherapist or osteopath. Often used manual therapies include spinal manipulative therapy (SMT), which is recommended in several clinical guidelines for management of back pain, mostly for acute low back pain (LBP) but also for chronic LBP. Despite the clinical benefits of SMT, the mechanisms underlying its effectiveness are poorly understood. Several mechanisms of action have been proposed including biomechanical and neurophysiological effects observed on spinal and supraspinal levels with unclear relationship to potential analgesic effects. Furthermore, non-specific effects such as placebo effects can strongly influence treatment outcomes and are difficult to control as consensus is lacking regarding the "active" agent of SMT, making it challenging to design an adequately controlled and blinded study.

A potential biological mechanism underlying the effectiveness of SMT might be related to sustained changes in lumbar proprioceptive function following repeated mechanical pressure on spinal tissues. In support of this, evidence from animal studies indicates that SMT comparable forces applied to the spine increase the discharge frequency of proprioceptive afferents in anesthetized cats, pointing towards an immediate effect of SMT on the activity of proprioceptive afferents. Proprioception is sub-served by mechanoreceptors on superficial and deep tissues. Located in the muscle belly parallel to the extrafusal muscle fibers, muscle spindles represent the main transmitters of proprioceptive information. Proprioceptive deficits have been suggested to provoke LBP through sensorimotor incongruence, abnormal loading across joint surfaces, and spinal instability due to less finely tuned muscular control, potentially causing sensorimotor dysfunction and degenerative processes in spinal tissues. In humans, there is anecdotal evidence that an SMT-induced repetitive barrage of proprioceptive input results in pain reduction and improves perceived function that might help to prevent LBP. However, a potential sustained and specific effect of SMT on lumbar proprioceptive function has not been systematically tested.

How one can test lumbar proprioceptive function in humans? Impairments in lumbar proprioception have been reported in LBP patients but only in sitting positions and mostly using proxy measures of proprioceptive function such as joint repositioning sense (JRS) and threshold to detect passive motion (TTDPM). The validity of these measures has been questioned as they measure position- and velocity-related proprioceptive sensation and the JRS is additionally influenced by motor skills and memory effects. Proprioceptive function can also be tested by assessing balance control (postural sway). Balance control presupposes a complex interplay involving the precise integration of proprioceptive inputs and motor outputs that can be tracked by analyzing postural sway on a force plate, a methodology that has been often used to assess differences in balance control in many diseases and conditions, including LBP. However, postural sway has been shown to be insensitive to changes of lumbar proprioceptive function, perhaps because postural sway relies on afferent input from various body locations and tissues. This can be overcome with a more direct assessment of proprioceptive function, achieved by using vibrotactile stimulation in combination with balance control measures. Vibration applied at frequencies between 60-80Hz (and amplitudes between 0.5-1mm) to muscles can selectively disturb proprioceptive signaling (mediated through primary (Ia) and secondary (II) muscle spindle afferents), affecting balance control by provoking corrective movements, often assessed through changes of the center of pressure (COP) in anterior-posterior direction. When endogenous or environmental conditions change, as in the instance of vibrotactile stimulation applied to the muscle, the balance control system must identify and selectively focus on sensory inputs providing the most reliable information, a process called sensory reweighting. Under normal conditions and while standing on a stable surface, healthy individuals rely on proprioceptive signals originating from ankle and paraspinal muscles. In contrast, standing on an unstable support surface (e.g. foam pad) forces individuals to rely less on ankle proprioception while up-weighting proprioceptive signals from paraspinal muscles. Differences in proprioceptive reweighting have been observed between healthy subjects and LBP patients by applying paraspinal and ankle muscle vibrotactile stimulation during a balance control task. Namely, during vibrotactile stimulation, individuals with recurrent LBP demonstrated an increased reliance on ankle proprioceptive signals compared to healthy subjects who up-weighted the proprioceptive signals from the paraspinal muscles (while down-weighting those from the ankle muscle to control postural balance). Importantly, a more "ankle-focused" strategy while standing on a stable support surface seems to increase the risk for developing or having recurrences of mild LBP within a time period of two years in young healthy individuals.

To test potential specific and sustained effects of SMT on lumbar proprioceptive function, the investigators aim to 1) assess SMT-induced changes in proprioceptive weighting (PW) over a two-week period and 2) use a rigorously controlled approach to control for non-specific effects. The planned experiments will be performed in healthy subjects because this will demonstrate a potential specific effect of SMT on lumbar proprioceptive function in a straight-forward manner without the need to control for possible confounding effects of pain/nociception on proprioception as it would be the case for pain patients. This will allow to draw conclusions w.r.t. an isolated effect of SMT on lumbar proprioceptive function, providing a clear mechanism for SMT-induced changes in sensorimotor function and a solid basis for further investigations in different LBP populations.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The study design consists of a four-arm (1:1:1:1 ratio) randomized controlled trial.The study design consists of a four-arm (1:1:1:1 ratio) randomized controlled trial.
Masking:
Triple (Participant, Care Provider, Outcomes Assessor)
Masking Description:
The data collection and analysis will be conducted by a research assistant blind to treatment allocation. The study subjects will be blinded with respect to the hypothesis.
Primary Purpose:
Basic Science
Official Title:
Does Spinal Manipulation Therapy Impact Lumbar Proprioception? A Double-blind Randomized Controlled Trial Examining the Influence of Spinal Manipulative Therapy (SMT) Versus a Sham and Non-sham Control Intervention on Proprioceptive Function
Anticipated Study Start Date :
Apr 1, 2022
Anticipated Primary Completion Date :
Apr 1, 2024
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: either lumbar manipulation (LMANIP)

LMANIP will consist of high velocity low amplitude (HVLA) SMT at the L4/L5 motion segment. LMANIP consists of two HVLA impulses, applied in side-posture on the right and left side (order pseudorandomized).

Procedure: spinal manipulation
intervention will consist of either lumbar manipulation, thoracic manipulation or lumbar mobilisation

Active Comparator: thoracic manipulation (TMANIP)

TMANIP will consist of high velocity low amplitude (HVLA) SMT at the T4/5 motion segment. TMANIP consists of supine SMT to the right and left (order pseudorandomized) using a thenar contact at facet joint level T4/5

Procedure: spinal manipulation
intervention will consist of either lumbar manipulation, thoracic manipulation or lumbar mobilisation

Sham Comparator: lumbar mobilisation (LMOB)

LMOB will be applied with the same positioning as in the LMANIP procedure, but instead of a thrust, a slow, a slow, passive mobilization without impulse will be applied

Procedure: spinal manipulation
intervention will consist of either lumbar manipulation, thoracic manipulation or lumbar mobilisation

No Intervention: No intervention

A natural history arm will serve to further control for potential specific and non-specific effects of TMANIP and LMOB. Subject will rest in side-lying position for the same duration as during the active interventions.

Outcome Measures

Primary Outcome Measures

  1. Postural sway (mm) [15 minutes]

    Postural sway will be measured using a force plate system

  2. Proprioceptive weighting ratio (value between 0 and 1) [15 minutes]

    The proprioceptive weighting ration will be calculated based on postural sway during vibrotactile stimulation on the ankle and paraspinal muscles

Secondary Outcome Measures

  1. Tampa-Scale for Kinesiophobia for the general population (TSK-G) questionnaire score [10 minutes]

    The original 17-item version of the TSK-G creates scores ranging between 17 and 68 higher scores indicating more fear of movement

  2. Belief score influence of manipulation on balance control [1 minute]

    Subjects will be asked to rate how much they belief a manual intervention will affect their balance control (0 = no influence, 10 = maximal influence)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Aged between 18 and 50

  • No chiropractic intervention (or similar) in the last 3 months

  • No episode of musculoskeletal pain in the past 3 months

  • No history of chronic pain (longer than 3 months)

  • No history of vestibular disorders

Exclusion Criteria:
  • Excessive consumption of alcohol or consumption of other drugs or analgesics within the last 24 h

  • Pregnancy

  • Prior foot/ankle or spine surgery

  • Any neuromuscular diseases that might affect gait and posture and injuries of the motor system with permanent deformities

  • Body mass index (BMI) > 30 kg/m2

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Balgrist University Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Michael Meier, Principal Investigator, Balgrist University Hospital
ClinicalTrials.gov Identifier:
NCT04869514
Other Study ID Numbers:
  • Project Nexus
First Posted:
May 3, 2021
Last Update Posted:
Mar 2, 2022
Last Verified:
Mar 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Mar 2, 2022