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Post-Traumatic Headache clinical trials

View clinical trials related to Post-Traumatic Headache.

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NCT ID: NCT06466499 Not yet recruiting - Clinical trials for Posttraumatic Headache

Non-pharmacological Treatment of Patients at Risk of Developing Persistent Posttraumatic Headache

Start date: August 1, 2024
Phase: N/A
Study type: Interventional

The goal of this mixed method study is to test and evaluate the effect of an early interdisciplinary non-pharmacological treatment of patients at risk of developing persistent posttraumatic headache in order to prevent the development of persistent posttraumatic headache and thereby, reduce persistency and improve the quality of life. Furthermore, to gain knowledge on and a deeper understanding of the patients' perspective and experience of the treatment. The project consists of 3 sub studies: 1. A feasibility study; with the purpose of exploring the feasibility of an early non-pharmacological intervention for patients with persistent posttraumatic headache after mild traumatic brain injury. 2. An experimental design; a randomized controlled trial to evaluate the effect of the early non-pharmacological treatment. 3. A qualitative focus group interview study; to get a more nuanced knowledge of patients' experience with the non-pharmacological treatment related to post traumatic headache.

NCT ID: NCT06452641 Not yet recruiting - Clinical trials for Cervicogenic Headache

Effects of Jones Technique and Cross Friction Massage on Cervicogenic Headache.

Start date: June 2024
Phase: N/A
Study type: Interventional

Cervicogenic headache is a very incessant issue that is often faced by the general population. Cervicogenic headache is a significant issue in patients with upper cervical dysfunction. However, its physical therapy management is a subject of debate. As the Comparative effects of Jones technique and cross-friction massage have never been investigated in patients with cervicogenic headache and neck pain, this study aims to investigate the effects of these treatments on two study groups (Group A&B) respectively.

NCT ID: NCT06434051 Not yet recruiting - Clinical trials for Cervicogenic Headache

The Effect of Traditional Chinese Cervical Manipulation for Cervicogenic Headache: a Pilot Randomized, Single-blind, Placebo-controlled Trial

Start date: July 1, 2024
Phase: N/A
Study type: Interventional

Background Cervical spondylosis is a prevalent condition. Studies has shown that it is a leading cause for headache, which is termed cervicogenic headache (CGH). The prevlance of CGH among severe headache is 17.5%. While conventional treatments, such as physical therapy and surgery, is effective in controlling symptoms, the effect was found to be short-lasting. There is existing clinical evidence supporting traditional Chinese cervical manipulation (CCM) as a viable treatment for CGH. Objective To preliminarily assess the feasibility, safety, and effectiveness of CCM on patients with CGH, and to optimize parameters for a future large-scale trial. Method This study is a pilot randomized, controlled, single-blind trial. 84 participants will be randomized evenly to receive either CCM or sham manipulation for 4 weeks. Outcome measurements will be conducted at baseline, week 2, week 4 and week 8 on cervical functional disability, cervical range of motion, and data on headache onset and painkiller assumption. Adverse events will be recorded using the Common Terminology Criteria for Adverse Events (CTCAE).

NCT ID: NCT06245967 Not yet recruiting - Dizziness Clinical Trials

Frequency Specific Microcurrent Therapy for Mild Traumatic Brain Injury

Start date: February 15, 2024
Phase: N/A
Study type: Interventional

Patients with mild traumatic brain injury (mTBI) may experience spontaneous recovery within 7-10 days, but some continue to exhibit symptoms such as headache, dizziness, vertigo, poor concentration, and cognitive dysfunction. Effective treatments for these symptoms are currently lacking. Frequency Specific Microcurrent(FSM) has received approval from the U.S. FDA for use in neuroinflammatory conditions. Our study aims to evaluate the efficacy of FSM by using FSM device ,IS02LCDs Stimulator (Ru Yi Health ltd. Co,Taiwan R.O.C), on symptom improvement in 52 patients with mild TBI

NCT ID: NCT05952115 Not yet recruiting - Clinical trials for Cervicogenic Headache

Efficacy of Lumbar Motor Control Training in Treatment Of Patients With Cervicogenic Headache

CGH
Start date: July 16, 2023
Phase: N/A
Study type: Interventional

this study will be conducted to investigate the effect of lumbar motor control training exercise on headache frequency, duration, intensity and neck functional disability in cervicogenic headache patients

NCT ID: NCT05697445 Not yet recruiting - Clinical trials for Cervicogenic Headache

Combined Effect Of Cranial And Cervical Mobilization In Patients With CGH

Start date: February 2023
Phase: N/A
Study type: Interventional

- The purposes of this study are: - To investigate the combined effect of cranial and cervical mobilization in patient with cervicogenic headache and there effect on : 1. Perceptive neck pain intensity 2. Perceptive headache intensity 3. pain by pressure 4. frequency of headache episodes 5. duration of headache episodes 6. Medications uptakes

NCT ID: NCT05658627 Not yet recruiting - Clinical trials for Cervicogenic Headache

Hamstring Active Release Technique in Cervicogenic Headache

Start date: April 2023
Phase: N/A
Study type: Interventional

It has been suggested that the suboccipital muscles are a causative factor in both cervicogenic neck pain and headache. Hamstrings and sub-occipital muscles are connected by a neural system and sub-occipital muscles pass through the dura Mater. Increased tension and shortening of the hamstring's muscles can cause neck and shoulder pain. In addition, when the muscles around the neck are tensed, the muscles in the limbs are also tensed, so that if the tone of the hamstring muscles is decreased, SLR test score increased, and the tone of the sub-occipital muscles is reduced. Active release technique is found to have an effect on hamstring flexibility.

NCT ID: NCT05545423 Not yet recruiting - Clinical trials for Cervicogenic Headache

Effect of Instrument-Assisted Soft Tissue Mobilization on Proprioception and Disability in Patients With Cervicogenic Headache

IASTM
Start date: September 30, 2022
Phase: N/A
Study type: Interventional

This study will be conducted to investigate the effect of instrument assisted soft tissue mobilization technique In pain intensity, frequency of headache, medication Uptake, Suboccipital movement in flexion and extension, rounded shoulder, forward head posture and proprioception of cervical spine in cases of cervicogenic headache related to trigger points and myofascial restrictions when combined with conventional physical therapy modalities.

NCT ID: NCT05446649 Not yet recruiting - Clinical trials for Cervicogenic Headache

Dry Needling Versus Instrumented Assisted Soft Tissue Mobilization In the Patient With Cervicogenic Treatment Headache

DN
Start date: July 5, 2022
Phase: N/A
Study type: Interventional

the aim of this study is to investigate the efficacy of Dry Needling Versus Instrumented Assisted Soft Tissue Mobilization In the Patient With Cervicogenic Treatment Headache

NCT ID: NCT05444296 Not yet recruiting - Headache Clinical Trials

Superficial Dry Needling for Cervicogenic Headache

Start date: July 5, 2022
Phase: N/A
Study type: Interventional

It is unknown if applying superficial dry needling to the trigeminal innervation field improves pain and disability for patients with cervicogenic headaches. The aim of this study is to determine if superficial dry needling of the trigeminal innervation field improves pain, neck mobility, and disability in patients with cervicogenic headaches. It will also be examined if psychosocial factors such as stress, anxiety, depression and self efficacy influence improvements in pain, range of motion and neck disability.