Transcranial Direct Current Stimulation in Conjunction With Individualized Physical Therapy for Individuals With Chronic Knee Pain

Knee Pain Chronic Clinical Trial

Official title:

Transcranial Direct Current Stimulation in Conjunction With Individualized Physical Therapy for Individuals With Chronic Knee Pain

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT06132412
• Other study ID #: 2023-1323
• Status: Not yet recruiting
• Phase: N/A
• Start date: January 1, 2024
• Est. completion date: January 1, 2025

Study information

• Verified date: November 2023
• Source: University of Illinois at Chicago
• Contact: Mariah Balinski
• Phone: 6308634273
• Email: balinsk1[@]uic.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Background: There is a high prevalence of chronic pain in the US, with nearly half of adults experiencing chronic pain. Chronic pain is associated with impaired mobility, specifically ambulation. Treatment for chronic knee pain is complex given that pain is not only due to peripheral sources, but also due to alterations of the central nervous system (CNS). Majority of physical therapy (PT) interventions involve a bottom-up approach targeting the peripheral pain sources and many patients (~66%) do not respond to this treatment approach. Noninvasive brain stimulation techniques such as transcranial direct current stimulation (tDCS) is a novel and promising option for a top-down intervention that can have neuromodulatory effects on the CNS and may better target central factors associated with chronic pain. Purpose: To determine if tDCS delivered to the primary motor cortex in conjunction with individualized PT will result in greater improvements in pain and function compared to sham tDCS with individualized PT in individuals with chronic knee pain. Methods: This study will be performed at outpatient PT clinics at the University of Illinois Hospital. Eligible participants will include patients with chronic knee pain (duration > 3 months) who have not undergone surgery to this area and are scheduled to receive formal PT intervention. Subjects will be randomized to the active tDCS + PT group or sham tDCS + PT group and will receive the intervention for 8 sessions. Outcomes include pain ratings, pressure pain thresholds, patient specific functional scale, lower extremity functional scale, quadriceps strength, knee range of motion, 2-minute walk test, 5 time sit to stand, patient health questionnaire-2, and Central Sensitization Inventory. Impact: The use of adjuvant therapies such as tDCS have the potential to optimize rehabilitation treatment for individuals with chronic pain by offering a more comprehensive treatment that targets peripheral and central sources of pain.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 30
• Est. completion date: January 1, 2025
• Est. primary completion date: January 1, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age >/= 18 years old

• Knee pain

• Knee pain duration >/= 3 months

Exclusion Criteria:

General exclusion criteria

• History of surgery on affected knee

• Pregnant

tDCS exclusion criteria

• Skin hypersensitivity

• History of contact dermatitis

• Any other skin or scalp condition that could be aggravated by tDCS

• Previous adverse reactions to tDCS

Related Conditions & MeSH terms

• Knee Pain Chronic

Intervention

Device:
• transcranial direct current stimulation
Transcranial direct current stimulation (tDCS) is a form of noninvasive brain stimulation that can have neuromodulatory effects on central nervous system structures, specifically the primary motor cortex (M1), and can potentially target maladaptive plasticity and nociplastic sources of pain. There is both anodal and cathodal tDCS, anodal stimulation increases excitability of the cortex whereas cathodal stimulation decreases excitability. At the synaptic level, anodal tDCS induces effects that mimic long term potentiation (LTP), while cathodal tDCS results in long term depression.

Other:
• physical therapy
Participants will receive individualized and impairment-based physical therapy treatment for their knee pain. This treatment can involve manual therapy, exercise or balance training depending on their particular needs.

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
University of Illinois at Chicago

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Recruitment ratio	We will record the number of patients screened and enrolled in the study.	through study completion, an average of 1 year
Primary	Pain (NPRS)	This will be measured subjectively using the Numeric Pain rating scale (NPRS). The PT or key research personnel with ask the participant their pain rating using a 0-10 scale. They will ask the current pain intensity rating, highest and lowest pain intensity rating in the past 2 week period.	baseline, every follow-up session through study completion
Primary	Two-minute walk test (2MWT)	Distance walked, number of rest breaks and the assistive device(s) used during a 2MWT will be measured. From this test walking speed can also be calculated.	baseline, at final intervention session
Secondary	Pressure pain threshold (PPT)	PPT will be obtained with an electronic pressure algometer and the pressure will be recorded in kPa to allow for comparison to norms	baseline, at final intervention session
Secondary	central sensitization inventory (CSI)	CSI is a self-report questionnaire that will be used as a secondary outcome to identify patients that may have symptoms related to central sensitization or nociplastic pain which may allow for subgroup analysis of data to occur	baseline, at final intervention session
Secondary	Lower extremity functional scale (LEFS)	self-report questionnaire where participants will rate the difficulty level they have with various daily mobility tasks	baseline, at final intervention session
Secondary	Patient specific functional scale (PSFS)	The PSFS is a self-report outcome measure that is individualized to the patient's specific activity impairments. The participant will choose 3 activities that are limited or difficult for them due to their knee pain and then will rate the level of difficulty of each task. On this scale, 0 means that the participant is unable to complete the activity at all and 10 means that the participant is able to perform the activity at the same level as before the injury or problem.	baseline, at final intervention session
Secondary	Five time sit to stand (5STS)	5STS will time the amount of time it takes for the participant to stand up and sit down five times as fast as they can from a standard chair without the use of their upper extremities if possible. If participants require upper extremity support to complete the task then this will be documented	baseline, at final intervention session
Secondary	knee range of motion (ROM)	): Knee flexion and extension ROM will be measured with the patient in a supine position if possible. If participants have knee ROM measured in a position other than supine this will be documented.	baseline, at final intervention session
Secondary	quadriceps strength	Quadriceps strength will be assessed using a hand-held dynamometer with the patient in a seated position	baseline, at final intervention session
Secondary	Treatment adherence	Adherence to tDCS and physical therapy treatment will also be recorded.	through study completion, an average of 1 year
Secondary	tDCS satisfaction	Participants and clinicians involved in the study will also complete a survey following completion of the study regarding their impressions (positive and negative) regarding tDCS.	at final intervention session