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OpenTrials
Completed

NCT Number: NCT00179114

Vanderbilt University Spasticity Management Program Evaluation Plan

People with severe developmental disabilities frequently have comorbidities that make providing care to them more difficult. Spasticity is one such comorbidity. It produces increased muscle tone that can cause stiffness in joints and bodily contortions that can interfere with all of the major types of care provided to participants. Typically, care areas include splinting, hygiene, dressing, transfers, positioning, ambulation, and engaging in other functional activities. Moreover, persons with spasticity often experience pain.

Typically, spasticity is managed by health care providers using a combination of the following therapies:

* Physical / occupational therapy (PT / OT) * Oral medication * Botox injections * Intrathecal baclofen administered by the Medtronic SyncroMed pump (ITB) * Orthopedic / neurological surgery

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Key information

Conditions

Spasticity Developmental Disabilities Mental Disorders Muscle Hypertonia Muscle Spasticity Muscular Diseases Musculoskeletal Diseases Nervous System Diseases Neurodevelopmental Disorders Neurologic Manifestations Neuromuscular Manifestations Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Vanderbilt University Medical Center

Nashville, Tennessee, 37212, United States

About this study

As individuals are identified as appropriate participants for the Program and consent is obtained, the care team for each person, consisting of both medical and caregiver staff, will define up to three specific care area goals and related tasks for treatment. A comprehensive spasticity management program will then be developed for the individual. Clinical and outcome assessments at baseline and at follow-up will include measures of range of motion, global spasticity according to a modified Ashworth scale, and the time and number of staff required for the task. In addition, video will be obtained of caregivers performing each participant's care area tasks at baseline and follow-up to allow an independent external reviewer to judge task difficulty. Treatment will be provided as outlined by the spasticity management plan. Follow-up evaluations will be conducted when the participant is at least one year from their initial Botulinum injection, or are one year post-implant for ITB participants. When the participant is exited from the study, Survey Physician will be asked to rate the overall impact of the Program on each of the individual's care area tasks.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult with spasticity residing at Clover Bottom Developmental Center in Nashville, Tennessee.
  • Spasticity must interfere with daily functioning.
  • Care team must be able to identify at least one treatment goal for the potential participant.

Exclusion criteria

  • Family or guardian is unwilling to provide written informed consent.
  • Spasticity does not interfere with patient's day-to-day care.
  • Staff who provide daily care are unable to identify a clear treatment goal.

Treatment and study plan

Botulinum Toxin Type A

Drug

Intrathecal baclofen administered by the Medtronic SyncroMed(TM) pump (ITB)

Drug

Primary outcomes

  1. Total time (in seconds) spent by caregivers to complete a defined care area task at one year followup.

  2. Categorical rating by blinded, independent reviewer of baseline and one-year care area task videos.

Secondary outcomes

  1. Range of motion score for each care area goal, assigned by physical therapist and compared at baseline vs. one-year followup.

  2. Differences in the number of hospital admissions 12 months pre- and 12 months post-program.

  3. Differences in costs associated with caregiving 12 months pre- and 12 months post-treatment.

  4. Difference in Physician's global assessment of spasticity at baseline and one-year followup.

Sponsors and collaborators

Lead sponsor

Vanderbilt University

Other

Collaborators

  • Allergan
  • Medtronic

Registry information

Important dates

Study start
2002
Study completion
2006
First posted
Sep 15, 2005
Registry last updated
Aug 20, 2007

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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