NCT06374862

Brief Summary

In this study, the investigators will examine the effect of manual therapy on the thoracic spine and its impact on the muscular strength gain of the thoracic extensors. Treatment with manual therapy, as described by Maitland, consists of a specific mobilization of the thoracic spine in the postero-anterior direction on the transverse and spiny processes of the thoracic vertebrae. To ensure the relevance of the measures, and to better control the occurrence of biases inherent to the practice of manual therapy, the investigators constituted three distinct groups: an intervention group, a control group and a group without intervention. In short, this methodology will allow us to explore in detail the effects of specific spinal mobilization on motor control, while taking into account placebo response elements and natural variations in the results

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
156

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Mar 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 28, 2024

Completed
19 days until next milestone

First Submitted

Initial submission to the registry

April 16, 2024

Completed
3 days until next milestone

First Posted

Study publicly available on registry

April 19, 2024

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 28, 2025

Completed
4 months until next milestone

Study Completion

Last participant's last visit for all outcomes

February 16, 2026

Completed
Last Updated

March 31, 2026

Status Verified

May 1, 2025

Enrollment Period

1.6 years

First QC Date

April 16, 2024

Last Update Submit

March 26, 2026

Conditions

Keywords

Musculoskeletal ManipulationsRange of MotionMuscle Strengthperipheral joints in upper quarters

Outcome Measures

Primary Outcomes (1)

  • electrical activity assessment of the spine extensor muscles using EMG

    1 hour

Study Arms (3)

Interventional

EXPERIMENTAL

This study is of an interventional nature, because the investigators want to objectively assess the impact of specific mobilization on neuromuscular functioning, thanks to surface EMG, before and after a specific mobilization of the spine.

Other: mobilization

control

SHAM COMPARATOR

This approach will help to determine whether there is spontaneous modulation of neuromuscular activity in the absence of intervention. Thus, the investigators can distinguish the effects of intervention from natural variations in the healthy subject.

Other: no effect

no interventional

NO INTERVENTION

A control group was also integrated to assess whether a mobilization identified as "no effect" could modulate neuromuscular activity by a placebo effect. This approach will allow to disentangle the real effects of mobilization from those that could result from psychomotor responses

Interventions

specific mobilization on neuromuscular functioning, thanks to surface EMG, before and after a specific mobilization of the spine

Interventional

a mobilization identified as "no effect" could modulate neuromuscular activity by a placebo effect.

control

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Ages 18 to 65,
  • healthy volunteer,
  • membership in a social security scheme

You may not qualify if:

  • Severe spinal trauma within the last 6 months
  • history of low back pain, back pain, and/or neck pain within the last 6 months,
  • history of spinal surgery,
  • history of chronic systemic disease (cardiac, respiratory, diabetes, etc.),
  • volunteer with Pacemaker, history of rheumatological pathology (rheumatoid arthritis, ankylosing spondylitis, Scheuermann's disease, etc.),
  • patient under guardianship,curatorship, safeguard of justice, patient deprived of liberty, pregnant woman and patient without Red Flags Social Security described in literature.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU Amiens Picardie

Amiens, Picardie, 80054, France

Location

MeSH Terms

Interventions

No-Observed-Adverse-Effect Level

Intervention Hierarchy (Ancestors)

Toxicity TestsInvestigative TechniquesToxicological PhenomenaPharmacological and Toxicological PhenomenaPhysiological Phenomena

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 16, 2024

First Posted

April 19, 2024

Study Start

March 28, 2024

Primary Completion

October 28, 2025

Study Completion

February 16, 2026

Last Updated

March 31, 2026

Record last verified: 2025-05

Data Sharing

IPD Sharing
Will not share

Locations