Cervical DystoniaNCT01671527
Insights Into Deep Brain Stimulation (DBS) for Cervical Dystonia
An observational study of Cervical Dystonia, run by University of Florida at 1 site in United States.
Trial summary
The purpose of this research study is to determine the physical brain changes in people with cervical dystonia after deep brain stimulation (DBS) surgery and as compared to healthy controls. We will do this by measuring your body's response to transcranial magnetic stimulation (TMS) before and/or after DBS surgery. Read more about this study
- Who is it for?
- Ages 18 to 80 yearsHealthy volunteers can take part
- Conditions the study is for
- Cervical Dystonia
- What is being tested?
- Transcranial magnetic stimulation (TMS)
- Type of treatment
- Surgery or procedure
- How many people
- 29 participants
- Where
- 1 siteUnited States
- Study dates
- Aug 2012to Jun 2016
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 80 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Study population: Subjects will be recruited from the University of Florida Center for Movement Disorders \& Neurorestoration out-patient population, patient care meetings, the UFMDC research database, and during the course of normal clinical care. Additionally, we plan to enroll subjects from other DBS centers. Patients who are diagnosed with primary (or predominantly primary) cervical dystonia and are candidates for DBS surgery, or who have already had DBS surgery, will be identified as candidates for this research study. Control subjects will be recruited via advertising flyers in the local community.
Who may be able to join
- Between the ages of 18-80 years
- Diagnosis confirming primary (or predominantly primary) cervical dystonia
- Currently treated with medications and (in view of the treating neurologist) has not responded well and is deemed a candidate for DBS surgery; enrolled in the evaluation process for DBS surgery, or
- DBS surgery within the last 3 months, or
- DBS surgery 6 months or more prior, or
- Ineligible or not planning to undergo DBS surgery (dystonia control cohort only)
Who cannot join
- Implanted pacemaker, medication pump, vagal stimulator, TENS unit or ventriculoperitoneal shunt
- Family or personal history of medication refractory epilepsy
- Pregnancy
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Pathophysiological Insights Into STN DBS for Primary Cervical Dystonia
The purpose of this research study is to determine the physical brain changes in people with cervical dystonia after deep brain stimulation (DBS) surgery and as compared to healthy controls. We will do this by measuring your body's response to transcranial magnetic stimulation (TMS) before and/or after DBS surgery.
TMS is a non-invasive procedure during which you sit in a chair that looks like one you would find at the dentist's office. A nerve stimulator is placed on the wrist of the right hand to stimulate the median nerve; the intensity of the nerve stimulator is gradually increased until the right thumb begins to twitch. A magnetic coil is placed on the scalp on one side of the head, overlying the brain's motor cortex, to stimulate the brain's output to the muscles in the opposite hand.
If you are a control subject, and therefore will not/have not have DBS surgery, we will measure the body's response to TMS for comparison purposes. We expect that the electrical differences in the brain may be related to the physical benefits some patients with primary cervical dystonia receive from DBS surgery.
Read the detailed description
Subjects will participate in 1-3 visits, based on eligibility, as described below:
Study Visit 1: Baseline
- This visit applies to subjects with cervical dystonia who are planning DBS surgery in the next 1-4 weeks
- This visit applies to subjects with cervical dystonia who are not planning DBS surgery
- This visit (except #3) applies to healthy control subjects; this is the only visit for healthy control subjects
- A neurological examination with special attention to the sensory system will be performed. The sensory system is the system by which the brain receives and perceives feelings from different parts of the body.
- Women of child-bearing potential will be given a urine pregnancy test to evaluate pregnancy status.
- DYSTONIA SUBJECTS ONLY: Clinical assessment of dystonia will be performed by administering several scales and measures, including: the Toronto Western Cervical Dystonia Rating Scale (TWSTRS), the Short Form (SF-36) scale for quality of life assessment, Visual Analog Scale (VAS) for assessment of dystonia and pain severity, the Mini Mental Status Examination (MMSE) for cognitive testing, and the Beck Depression Inventory (BDI II), for evaluation of mood.
- We will determine your individual motor evoked potential (MEP) threshold before beginning the study treatment. Your MEP will be recorded from a muscle located between the right thumb and index finger on your right hand, and then on your left hand. MEP threshold refers to the amount of stimulation to the brain that is required to activate muscle cells enough to appear on an electromyography (EMG), which records electrical potential in muscle through electrodes placed on the skin.
- We will test your sensory system and its interaction with the motor cortex by using transcranial magnetic Stimulation (TMS). For these tests, you will sit in a chair that looks like one you would find at the dentist's office. A nerve stimulator will be placed at the wrist of your right hand to stimulate the median and ulnar nerves. The intensity of the nerve stimulator will be gradually increased until the right thumb begins to twitch. A magnetic coil will be placed on the scalp on the left side of your head, overlying the brain's motor cortex, to stimulate the brain's output to the muscles in the opposite hand. This procedure will be repeated using the left wrist and the right side of your head.
- We will spend an additional 30 minutes performing a protocol that allows for testing of plasticity changes in the brain. This protocol is called paired associative stimulation (PAS). The median nerve in your wrist and the TMS coil over your head undergo repeated paired stimulation. Such repeated pairing builds plasticity effect in the motor cortex. MEP, as explained earlier, is recorded before and after this protocol.
- Subjects who have provided consent will be videotaped during this visit.
Study Visit 2:
- This visit will be identical to Visit 1 for subjects with cervical dystonia who are not planning DBS
- This visit, as described below, applies to subjects with cervical dystonia who have had DBS less than 3 months prior
- This study visit involves 2 conditions and will be performed approximately 3 months after DBS surgery over a span of up to 3 days. For each condition your DBS stimulator will be kept either ON or OFF.
- A physical examination, including the clinical dystonia rating scales and TMS tests used during Visit 1, will be administered and recorded for both conditions.
- PAS, as described above for Visit 1, will be performed both ON and OFF stimulation to test the plasticity effects of DBS surgery.
- Additionally, women of childbearing potential will be given a urine pregnancy test to evaluate pregnancy status.
- Subjects who have provided consent will be videotaped.
Visit 3:
- This visit applies to subjects who have had DBS surgery 6 months or more prior
- The method and plan will be identical to that used during Visit 2.
- Conditions
- Cervical Dystonia
- Being tested
- Transcranial magnetic stimulation (TMS)
- Keywords
- Deep Brain Stimulation, DBS, Transcranial Magnetic Stimulation, TMS, Cervical Dystonia, Dystonia, Control, Healthy
- Medical subject headings
- Torticollis, Dystonia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Transcranial magnetic stimulation (TMS)Procedure or surgery
We will test the sensory system and its interaction with the motor cortex by using TMS. For these tests, you will sit in a chair that looks like one you would find at the dentist's office. A nerve stimulator will be placed on the wrist of your right hand to stimulate the median and ulnar nerves. The intensity of the nerve stimulator will be gradually increased until the right thumb begins to twitch. A magnetic coil will be placed on the scalp on the left side of your head, overlying the brain's motor cortex, to stimulate the brain's output to the muscles in the opposite hand. This procedure will be repeated using the left wrist and the right side of your head.
| Study group | Role | What they receive |
|---|---|---|
| Cervical Dystonia: DBS Subjects | Subjects who have undergone or plan to undergo DBS surgery for cervical dystonia Receives: Procedure: Transcranial magnetic stimulation (TMS) | |
| Cervical Dystonia: Control Subjects | Subjects who DO NOT plan to undergo DBS surgery for cervical dystonia Receives: Procedure: Transcranial magnetic stimulation (TMS) | |
| Healthy Controls | Healthy control subjects who do not have dystonia. Receives: Procedure: Transcranial magnetic stimulation (TMS) |
What is being measured
The primary outcome is the main question the study is designed to answer.
The body's response to transcranial magnetic stimulation (TMS)
The purpose of this research study is to determine the physical brain changes in people with cervical dystonia after deep brain stimulation (DBS) surgery. We will do this by measuring your body's response to transcranial magnetic stimulation (TMS) before and/or after DBS surgery, unless you are a control subject. If you are a dystonia control subject (not planning DBS), we will measure your body's response to TMS on two occasions. If you are healthy control subject, we will measure your body's response to TMS on one occasion.
These tests should help us learn whether the electrical changes in the brain have any relation to the physical benefits some patients with primary cervical dystonia receive from DBS surgery.
Measured: From 1 day to 10 months, based on eligibility
Secondary outcomes (1)
Clinical assessment of dystonia severity
Dystonia will be evaluated at each study visit using: the Toronto Western Cervical Dystonia Rating Scale (TWSTRS); the Visual Analogue Scale (VAS) for assessment of dystonia pain and severity
Measured: 10 minutes at each study visit
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted23 Aug 2012 (estimated)
- Study startAug 2012
- Primary completionMar 2016
- Study completionJun 2016
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for Cervical DystoniaStudies of the same condition, open and under way.
- More trials run by University of FloridaThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Case-control
- Time perspective
- Prospective
- Enrolment
- 29 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Florida
- Sponsor type
- University, hospital or other
- Collaborators
- National Institutes of Health (NIH), Dystonia Coalition
- Responsible party
- Sponsor
- Investigators
- Aparna Wagle Shukla, MD, Principal investigator, University of Florida
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT01671527
- Sponsor's protocol ID
- 3142012
- Other IDs
- KL2TR000065
- Status last verified
- Jun 2016
- First submitted
- 20 Aug 2012
- Last updated
- 13 Jun 2016
- Results posted
- No
- Data monitoring committee
- Yes
Publications
Wagle Shukla A, Ostrem JL, Vaillancourt DE, Chen R, Foote KD, Okun MS. Physiological effects of subthalamic nucleus deep brain stimulation surgery in cervical dystonia. J Neurol Neurosurg Psychiatry. 2018 Dec;89(12):1296-1300. doi: 10.1136/jnnp-2017-317098. Epub 2018 Jan 11.
PubMed 29326293
Study at a glance
From the registry record, last updated by the sponsor on 13 Jun 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Pathophysiological Insights Into STN DBS for Primary Cervical Dystonia
- ClinicalTrials.gov ID
- NCT01671527
- Acronym / sponsor ID
- 3142012
- Conditions
- Cervical Dystonia
- Keywords
- Deep Brain Stimulation, DBS, Transcranial Magnetic Stimulation, TMS, Cervical Dystonia, Dystonia, Control, Healthy
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 29 participants (actual)
- Lead sponsor
- University of FloridaUniversity, hospital or other
- Collaborators
- National Institutes of Health (NIH), Dystonia Coalition
- Study start
- Aug 2012
- Primary completion
- Mar 2016 (actual)
- Study completion
- Jun 2016 (actual)
- First posted
- 23 Aug 2012 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this research study is to determine the physical brain changes in people with cervical dystonia after deep brain stimulation (DBS) surgery and as compared to healthy controls. We will do this by measuring your body's response to transcranial magnetic stimulation (TMS) before and/or after DBS surgery.
TMS is a non-invasive procedure during which you sit in a chair that looks like one you would find at the dentist's office. A nerve stimulator is placed on the wrist of the right hand to stimulate the median nerve; the intensity of the nerve stimulator is gradually increased until the right thumb begins to twitch. A magnetic coil is placed on the scalp on one side of the head, overlying the brain's motor cortex, to stimulate the brain's output to the muscles in the opposite hand.
If you are a control subject, and therefore will not/have not have DBS surgery, we will measure the body's response to TMS for comparison purposes. We expect that the electrical differences in the brain may be related to the physical benefits some patients with primary cervical dystonia receive from DBS surgery.
Detailed description
Subjects will participate in 1-3 visits, based on eligibility, as described below:
Study Visit 1: Baseline
- This visit applies to subjects with cervical dystonia who are planning DBS surgery in the next 1-4 weeks
- This visit applies to subjects with cervical dystonia who are not planning DBS surgery
- This visit (except #3) applies to healthy control subjects; this is the only visit for healthy control subjects
- A neurological examination with special attention to the sensory system will be performed. The sensory system is the system by which the brain receives and perceives feelings from different parts of the body.
- Women of child-bearing potential will be given a urine pregnancy test to evaluate pregnancy status.
- DYSTONIA SUBJECTS ONLY: Clinical assessment of dystonia will be performed by administering several scales and measures, including: the Toronto Western Cervical Dystonia Rating Scale (TWSTRS), the Short Form (SF-36) scale for quality of life assessment, Visual Analog Scale (VAS) for assessment of dystonia and pain severity, the Mini Mental Status Examination (MMSE) for cognitive testing, and the Beck Depression Inventory (BDI II), for evaluation of mood.
- We will determine your individual motor evoked potential (MEP) threshold before beginning the study treatment. Your MEP will be recorded from a muscle located between the right thumb and index finger on your right hand, and then on your left hand. MEP threshold refers to the amount of stimulation to the brain that is required to activate muscle cells enough to appear on an electromyography (EMG), which records electrical potential in muscle through electrodes placed on the skin.
- We will test your sensory system and its interaction with the motor cortex by using transcranial magnetic Stimulation (TMS). For these tests, you will sit in a chair that looks like one you would find at the dentist's office. A nerve stimulator will be placed at the wrist of your right hand to stimulate the median and ulnar nerves. The intensity of the nerve stimulator will be gradually increased until the right thumb begins to twitch. A magnetic coil will be placed on the scalp on the left side of your head, overlying the brain's motor cortex, to stimulate the brain's output to the muscles in the opposite hand. This procedure will be repeated using the left wrist and the right side of your head.
- We will spend an additional 30 minutes performing a protocol that allows for testing of plasticity changes in the brain. This protocol is called paired associative stimulation (PAS). The median nerve in your wrist and the TMS coil over your head undergo repeated paired stimulation. Such repeated pairing builds plasticity effect in the motor cortex. MEP, as explained earlier, is recorded before and after this protocol.
- Subjects who have provided consent will be videotaped during this visit.
Study Visit 2:
- This visit will be identical to Visit 1 for subjects with cervical dystonia who are not planning DBS
- This visit, as described below, applies to subjects with cervical dystonia who have had DBS less than 3 months prior
- This study visit involves 2 conditions and will be performed approximately 3 months after DBS surgery over a span of up to 3 days. For each condition your DBS stimulator will be kept either ON or OFF.
- A physical examination, including the clinical dystonia rating scales and TMS tests used during Visit 1, will be administered and recorded for both conditions.
- PAS, as described above for Visit 1, will be performed both ON and OFF stimulation to test the plasticity effects of DBS surgery.
- Additionally, women of childbearing potential will be given a urine pregnancy test to evaluate pregnancy status.
- Subjects who have provided consent will be videotaped.
Visit 3:
- This visit applies to subjects who have had DBS surgery 6 months or more prior
- The method and plan will be identical to that used during Visit 2.
Study design
- Observational model
- Case-control
- Time perspective
- Prospective
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Cervical Dystonia: DBS Subjects | – | Procedure: Transcranial magnetic stimulation (TMS)Subjects who have undergone or plan to undergo DBS surgery for cervical dystonia |
| Cervical Dystonia: Control Subjects | – | Procedure: Transcranial magnetic stimulation (TMS)Subjects who DO NOT plan to undergo DBS surgery for cervical dystonia |
| Healthy Controls | – | Procedure: Transcranial magnetic stimulation (TMS)Healthy control subjects who do not have dystonia. |
Who may qualify
- Ages
- 18 to 80 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
- Study population
- Subjects will be recruited from the University of Florida Center for Movement Disorders \& Neurorestoration out-patient population, patient care meetings, the UFMDC research database, and during the course of normal clinical care. Additionally, we plan to enroll subjects from other DBS centers. Patients who are diagnosed with primary (or predominantly primary) cervical dystonia and are candidates for DBS surgery, or who have already had DBS surgery, will be identified as candidates for this research study. Control subjects will be recruited via advertising flyers in the local community.
Key inclusion criteria (6 listed)
- Between the ages of 18-80 years
- Diagnosis confirming primary (or predominantly primary) cervical dystonia
- Currently treated with medications and (in view of the treating neurologist) has not responded well and is deemed a candidate for DBS surgery; enrolled in the evaluation process for DBS surgery, or
- DBS surgery within the last 3 months, or
- DBS surgery 6 months or more prior, or
Key exclusion criteria (3 listed)
- Implanted pacemaker, medication pump, vagal stimulator, TENS unit or ventriculoperitoneal shunt
- Family or personal history of medication refractory epilepsy
- Pregnancy
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Transcranial magnetic stimulation (TMS)We will test the sensory system and its interaction with the motor cortex by using TMS. For these tests, you will sit in a chair that looks like one you would find at the dentist's office. A nerve stimulator will be placed on the wrist of your right hand to stimulate the median and ulnar nerves. The intensity of the nerve stimulator will be gradually increased until the right thumb begins to twitch. A magnetic coil will be placed on the scalp on the left side of your head, overlying the brain's motor cortex, to stimulate the brain's output to the muscles in the opposite hand. This procedure will be repeated using the left wrist and the right side of your head. | Procedure or surgery | Cervical Dystonia: Control Subjects, Cervical Dystonia: DBS Subjects, Healthy Controls |
Primary outcome
The body's response to transcranial magnetic stimulation (TMS)
Time frame: From 1 day to 10 months, based on eligibility
The purpose of this research study is to determine the physical brain changes in people with cervical dystonia after deep brain stimulation (DBS) surgery. We will do this by measuring your body's response to transcranial magnetic stimulation (TMS) before and/or after DBS surgery, unless you are a control subject. If you are a dystonia control subject (not planning DBS), we will measure your body's response to TMS on two occasions. If you are healthy control subject, we will measure your body's response to TMS on one occasion. These tests should help us learn whether the electrical changes in the brain have any relation to the physical benefits some patients with primary cervical dystonia receive from DBS surgery.
1 secondary outcome
Clinical assessment of dystonia severity
Time frame: 10 minutes at each study visit
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Jun 2016.
- Derived from this study: PubMed 29326293Wagle Shukla A, Ostrem JL, Vaillancourt DE, Chen R, Foote KD, Okun MS. Physiological effects of subthalamic nucleus deep brain stimulation surgery in cervical dystonia. J Neurol Neurosurg Psychiatry. 2018 Dec;89(12):1296-1300. doi: 10.1136/jnnp-2017-317098. Epub 2018 Jan 11.
- Dystonia CoalitionLink provided by the sponsor.
- National Institutes of Health (NIH)Link provided by the sponsor.
- UF Center for Movement Disorders \& NeurorestorationLink provided by the sponsor.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Aparna Wagle Shukla, MD principal investigator
University of Florida
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Cervical Dystonia, run by University of Florida at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 13 Jun 2016. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
The body's response to transcranial magnetic stimulation (TMS) (time frame: From 1 day to 10 months, based on eligibility). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT01671527, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Jun 2016.