# Identifying Early Responders to Dry Needling for Lower-Limb Spasticity in Multiple Sclerosis: A Secondary Responder Analysis of a Pilot Randomized Controlled Trial

**Authors:** Alberto Javier-Ormazábal, Marta González-Sierra, Montserrat González-Platas

PMC · DOI: 10.3390/brainsci16020240 · Brain Sciences · 2026-02-21

## TL;DR

A third of multiple sclerosis patients showed improvement after dry needling for spasticity, with early responders more likely to have relapsing-remitting MS and lower disability.

## Contribution

Identified early responders to dry needling in MS and linked response to disease type and baseline disability.

## Key findings

- Approximately one-third of MS patients showed clinically meaningful improvement after dry needling.
- Early responders were more likely to have relapsing–remitting MS and lower baseline disability.
- Dry needling may benefit a specific subgroup of MS patients rather than being a universal treatment.

## Abstract

What are the main findings?
Approximately one-third of ambulatory people with multiple sclerosis showed clinically meaningful improvement after a single session of dry needling for lower-limb spasticity.Early responders were more likely to have a relapsing–remitting disease course and lower baseline disability.

Approximately one-third of ambulatory people with multiple sclerosis showed clinically meaningful improvement after a single session of dry needling for lower-limb spasticity.

Early responders were more likely to have a relapsing–remitting disease course and lower baseline disability.

What are the implications of the main findings?
Dry needling may be a beneficial adjunctive intervention for a specific subgroup of patients with multiple sclerosis rather than a universal treatment.Responder-based analyses can support personalized rehabilitation strategies and inform patient selection in future clinical trials.

Dry needling may be a beneficial adjunctive intervention for a specific subgroup of patients with multiple sclerosis rather than a universal treatment.

Responder-based analyses can support personalized rehabilitation strategies and inform patient selection in future clinical trials.

Background/Objectives: Response heterogeneity limits the implementation of dry needling for spasticity in multiple sclerosis (MS). This secondary analysis aimed to identify early responders and explore predictors of response. Methods: We conducted a responder analysis of a pilot randomized, double-blind, sham-controlled trial (NCT05956119) including 18 ambulatory MS patients with spasticity, randomized to a single session of dry needling (n = 9) or sham (n = 9). Sensitive responder criteria were defined as improvement ≥ 2.0 s in Timed Up-and-Go, ≥5 points in MSQOL-54 physical component, or ≥10% in 25-Foot Walk Test at 4 weeks. Results: Using these criteria, 33.3% (3/9) of dry needling recipients were classified as responders versus 0% (0/9) in the sham group (p = 0.214). Responders were more frequently observed among participants with relapsing–remitting MS (100% vs. 40%, p = 0.090) and lower baseline disability (Expanded Disability Status Scale 3.4 vs. 4.4). A positive association was observed between baseline pyramidal subscore and physical quality-of-life change, although this did not reach statistical significance (r = 0.52, p = 0.150) in the active group. Conclusions: Approximately one-third of participants met predefined responder criteria following dry needling; however, these findings should be interpreted as preliminary signals derived from an exploratory, underpowered pilot analysis. These results are hypothesis-generating and require confirmation in adequately powered trials.

## Linked entities

- **Diseases:** multiple sclerosis (MONDO:0005301)

## Full-text entities

- **Diseases:** gait dysfunction (MESH:D020233), bleeding disorders (MESH:D006470), gait impairment (MESH:D020234), impaired motor control (MESH:D007174), fatigue (MESH:D005221), allergy (MESH:D004342), MS (MESH:D009103), neuromuscular impairments (MESH:D009468), Spasticity (MESH:D009128), injury to (MESH:D014947), inflammatory, demyelinating, and neurodegenerative disease (MESH:D019636), reduced mobility (MESH:D014086), skin infections (MESH:D007239), impaired balance (MESH:D060825), muscle weakness (MESH:D018908), sensory disturbances (MESH:D012678), DN (MESH:D015352), relapsing-remitting multiple sclerosis (MESH:D020529), hypertonia (MESH:D009122)
- **Chemicals:** Antispastic Medication (-), fampridine (MESH:D015761), baclofen (MESH:D001418)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

44 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938198/full.md

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Source: https://tomesphere.com/paper/PMC12938198