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The Brain Stimulation and Physical Therapy Study

Primary Purpose

Fall, Gait, Unsteady, Aging

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Real tDCS and Physical Therapy
Sham stimulation and Physical Therapy
Sponsored by
Hebrew SeniorLife
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fall

Eligibility Criteria

65 Years - undefined (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Ages 65 years old and above
  • Admitted to Physical Therapy for gait and balance training due to the high risk of falls

Exclusion Criteria:

  • Inability to stand or walk unassisted for 60 seconds
  • Severe cognitive impairment defined as a Montreal Cognitive Assessment (MoCA) score < 18
  • Any unstable medical condition
  • Any unstable psychiatric co-morbidity including major depressive disorder, schizophrenia or psychosis
  • Active cancer for which chemo/radiation therapy id being received
  • Significant vision and hearing problems that cannot be corrected with visual and hearing aids
  • Contraindications to tDCS, including seizure within the past two years, use of neuro-active drugs, the risk of metal objects in the brain, implanted medical devices, or the presence of dermatological conditions such as eczema on the scalp.

Sites / Locations

  • Hebrew Rehabilitation Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Real tDCS and Physical Therapy

Sham stimulation and Physical Therapy

Arm Description

This arm combines tDCS and Physical Therapy intervention. The real tDCS will be delivered before each physical therapy visit for up to 10 combined sessions. The tDCS montage was designed to target the left dorsal lateral prefrontal cortex (DLPFC) for around 20 minutes. The direct current delivered by any electrode will not exceed 2.0 milliamp(mA) and the total amount of current from all electrodes will not exceed 4 mA.

This arm combines sham stimulation and Physical Therapy intervention. The sham stimulation will be delivered before each physical therapy visit for up to 10 combined sessions. We will use an active sham stimulation in which very low-level currents (0.5 mA total) will be transferred between electrodes in close proximity on the scalp throughout the entire 20-minute session. This montage was designed to deliver currents not significantly influence their cortical tissue, but still, mimic the cutaneous sensations induced by tDCS over the same brain site (i.e. left DLPFC).

Outcomes

Primary Outcome Measures

Screening to enrollment ratio (%, 0-100, higher ratio means a better outcome)
The number of screenings needed to enroll one participant
Intervention adherence rate (%, 0-100, higher ratio means a better outcome)
Number of tDCS sessions completed
Adherence rate (%, 0-100, higher ratio means a better outcome)
The portion of enrolled participants who complete and adhere to the intervention who complete and adhere to the intervention
Side effects
The number, type, severity and duration of reported side effects
Change from baseline in the dual task cost to gait speed (reduced dual task cost after intervention means a better outcome)
The change from baseline in the degree to which performing a secondary cognitive task diminishes gait speed
Change from baseline in the dual task cost to standing postural sway speed (reduced dual task cost after intervention means a better outcome)
The change from baseline in the degree to which performing a secondary cognitive task diminishes the control of standing posture.
Change from baseline in Trail Making Test B - A (reduced time after intervention means a better outcome)
The change from baseline in cognitive executive function

Secondary Outcome Measures

Change from baseline in gait speed (increased value after intervention means a better outcome)
The change from baseline in gait speed
Change from baseline in gait variability (reduced value after intervention means a better outcome)
The change from baseline in gait speed
Change from baseline in gradual-onset continuous performance test (gradCPT) ( increased accuracy after intervention means a better outcome)
The change from baseline in cognitive sustained attention
Change from baseline in Timed Up-and-Go (TUG) (reduced time after intervention means a better outcome)
The change from baseline in overall mobility function
Change from baseline in Montreal Cognitive Assessment (MoCA) total score (increased score after intervention means a better outcome)
The change from baseline in global cognitive function

Full Information

First Posted
November 26, 2019
Last Updated
September 1, 2021
Sponsor
Hebrew SeniorLife
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1. Study Identification

Unique Protocol Identification Number
NCT04181658
Brief Title
The Brain Stimulation and Physical Therapy Study
Official Title
The Feasibility and Effectiveness of Combining Non-invasive Brain Stimulation and Physical Therapy to Improve Gait and Balance in Older Adults at Risk of Falling
Study Type
Interventional

2. Study Status

Record Verification Date
September 2021
Overall Recruitment Status
Completed
Study Start Date
October 22, 2019 (Actual)
Primary Completion Date
May 1, 2021 (Actual)
Study Completion Date
May 1, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hebrew SeniorLife

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This pilot work will determine the feasibility of tDCS intervention as an effective adjunct intervention to PT aimed at improving gait, balance, and mobility in older adults at risk of falling.
Detailed Description
Falls are correlated with both physical and cognitive declines in older adults. Recurrent fallers and those at high risk of falls are often referred to physical therapy (PT) for gait and balance training. Although physical therapists are aware of the importance of cortical control of gait and balance, there is no available tool to directly yet non-invasively intervene brain in the clinical setting. Transcranial direct current stimulation (tDCS) is a noninvasive and safe mean of modulating the excitability of specific brain regions and their connected neural networks. Our group and others have shown that tDCS intervention designed to facilitate the excitability of the left dorsal lateral prefrontal cortex (DLPFC) improves numerous aspects of executive function related to mobility in older adults. However, no studies to date have assessed the feasibility and effectiveness of applying tDCS as an adjunct to PT to improve gait and balance within the geriatric rehabilitation setting. This study aims to 1) assess the feasibility of implementing tDCS prior to each of their first 10 PT sessions, and 2) gather estimates of variability in outcomes related to gait, balance, cognition, and quality of life over time within older adults referred to PT for recurrent falls.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fall, Gait, Unsteady, Aging, Accidental Fall

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Real tDCS and Physical Therapy
Arm Type
Experimental
Arm Description
This arm combines tDCS and Physical Therapy intervention. The real tDCS will be delivered before each physical therapy visit for up to 10 combined sessions. The tDCS montage was designed to target the left dorsal lateral prefrontal cortex (DLPFC) for around 20 minutes. The direct current delivered by any electrode will not exceed 2.0 milliamp(mA) and the total amount of current from all electrodes will not exceed 4 mA.
Arm Title
Sham stimulation and Physical Therapy
Arm Type
Sham Comparator
Arm Description
This arm combines sham stimulation and Physical Therapy intervention. The sham stimulation will be delivered before each physical therapy visit for up to 10 combined sessions. We will use an active sham stimulation in which very low-level currents (0.5 mA total) will be transferred between electrodes in close proximity on the scalp throughout the entire 20-minute session. This montage was designed to deliver currents not significantly influence their cortical tissue, but still, mimic the cutaneous sensations induced by tDCS over the same brain site (i.e. left DLPFC).
Intervention Type
Other
Intervention Name(s)
Real tDCS and Physical Therapy
Other Intervention Name(s)
Real tDCS + PT
Intervention Description
The participant will receive 20-minute sessions of real tDCS before each physical therapy visit for up to 10 combined sessions, over approximately 6 weeks.
Intervention Type
Other
Intervention Name(s)
Sham stimulation and Physical Therapy
Other Intervention Name(s)
Sham stimulation + PT
Intervention Description
The participant will receive 20-minute sessions of sham stimulation before each physical therapy visit for up to 10 combined sessions, over approximately 6 weeks.
Primary Outcome Measure Information:
Title
Screening to enrollment ratio (%, 0-100, higher ratio means a better outcome)
Description
The number of screenings needed to enroll one participant
Time Frame
The whole data collection period (~ 6 months for the whole study)
Title
Intervention adherence rate (%, 0-100, higher ratio means a better outcome)
Description
Number of tDCS sessions completed
Time Frame
The whole data collection period (~ 6 months for the whole study)
Title
Adherence rate (%, 0-100, higher ratio means a better outcome)
Description
The portion of enrolled participants who complete and adhere to the intervention who complete and adhere to the intervention
Time Frame
The whole data collection period (~ 6 months for the whole study)
Title
Side effects
Description
The number, type, severity and duration of reported side effects
Time Frame
The whole data collection period (~ 6 months for the whole study)
Title
Change from baseline in the dual task cost to gait speed (reduced dual task cost after intervention means a better outcome)
Description
The change from baseline in the degree to which performing a secondary cognitive task diminishes gait speed
Time Frame
Before and after the intervention (~ 6 weeks per participant)
Title
Change from baseline in the dual task cost to standing postural sway speed (reduced dual task cost after intervention means a better outcome)
Description
The change from baseline in the degree to which performing a secondary cognitive task diminishes the control of standing posture.
Time Frame
Before and after the intervention (~ 6 weeks per participant)
Title
Change from baseline in Trail Making Test B - A (reduced time after intervention means a better outcome)
Description
The change from baseline in cognitive executive function
Time Frame
Before and after the intervention (~ 6 weeks per participant)
Secondary Outcome Measure Information:
Title
Change from baseline in gait speed (increased value after intervention means a better outcome)
Description
The change from baseline in gait speed
Time Frame
Before and after the intervention (~ 6 weeks per participant)
Title
Change from baseline in gait variability (reduced value after intervention means a better outcome)
Description
The change from baseline in gait speed
Time Frame
Before and after the intervention (~ 6 weeks per participant)
Title
Change from baseline in gradual-onset continuous performance test (gradCPT) ( increased accuracy after intervention means a better outcome)
Description
The change from baseline in cognitive sustained attention
Time Frame
Before and after the intervention (~ 6 weeks per participant)
Title
Change from baseline in Timed Up-and-Go (TUG) (reduced time after intervention means a better outcome)
Description
The change from baseline in overall mobility function
Time Frame
Before and after the intervention (~ 6 weeks per participant)
Title
Change from baseline in Montreal Cognitive Assessment (MoCA) total score (increased score after intervention means a better outcome)
Description
The change from baseline in global cognitive function
Time Frame
Before and after the intervention (~ 6 weeks per participant)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ages 65 years old and above Admitted to Physical Therapy for gait and balance training due to the high risk of falls Exclusion Criteria: Inability to stand or walk unassisted for 60 seconds Severe cognitive impairment defined as a Montreal Cognitive Assessment (MoCA) score < 18 Any unstable medical condition Any unstable psychiatric co-morbidity including major depressive disorder, schizophrenia or psychosis Active cancer for which chemo/radiation therapy id being received Significant vision and hearing problems that cannot be corrected with visual and hearing aids Contraindications to tDCS, including seizure within the past two years, use of neuro-active drugs, the risk of metal objects in the brain, implanted medical devices, or the presence of dermatological conditions such as eczema on the scalp.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
On-Yee Lo, PhD
Organizational Affiliation
Hebrew Rehabilitation Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hebrew Rehabilitation Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02131
Country
United States

12. IPD Sharing Statement

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The Brain Stimulation and Physical Therapy Study

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