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NCT02170779 · ClinicalTrials.gov registry record · Phase 2

Developing and Testing a Comprehensive MS Spasticity Management Program

A Phase 2 study, sponsored by VA Office of Research and Development.

Completed
Registry status
Phase 2
Development phase
40
Enrollment target

NCT02170779: Completed Phase 2 study, sponsored by VA Office of Research and Development.

NCT02170779 is a Phase 2 study that has completed, run by VA Office of Research and Development. The registered enrollment target is 40 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02170779, a Phase 2 study, has completed, sponsored by VA Office of Research and Development.

COMPLETED
Registry status
Phase 2
Development phase
40 participants
Enrollment target

Study Summary

This is a study to determine the impact of education and specific lower extremity stretches for MS-related spasticity. The study will evaluate the acceptance and efficacy of education and stretching using a randomized controlled pilot trial.

Primary Outcome

The MSWS-12 is a clinically validated and reliable tool that is flexible and simple enough to use clinically and in research. It captures patients' perspectives on their ambulatory disability on the following: standing, ability to run, need for support, moving around the home, concentration needed to walk, walking speed, maintaining balance, climbing stairs, walking distance, effort needed to walk, ability to walk, and gait. It is simple to administer and responsive to changes in patient perform

Interventions

  • OTHER Usual care
  • BEHAVIORAL Spasticity: Take Control

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2015-10
Est. Completion 2016-06
Phase Phase 2
VA Office of Research and Development

1,668 total trials

What the finished NCT02170779 record still lists

NCT02170779 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (70% lower).

The record links to 0 conditions, and to 2 interventions - of which Usual care is the first listed.

NCT02170779 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02170779 about?

NCT02170779 is a clinical study titled "Developing and Testing a Comprehensive MS Spasticity Management Program". This is a study to determine the impact of education and specific lower extremity stretches for MS-related spasticity. The study will evaluate the acceptance and efficacy of education and stretching using a randomized controlled pilot trial.

What is the current status of trial NCT02170779?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2015-10. Estimated completion is 2016-06.

What interventions are being tested in trial NCT02170779?

The interventions under investigation include: Usual care (OTHER), Spasticity: Take Control (BEHAVIORAL).

Who is sponsoring clinical trial NCT02170779?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02170779's enrollment target sits among peer trials

40 1362nd of 2000 higher than 542 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02170779, the US trial registry maintained by the National Library of Medicine. NCT02170779 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.