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NCT ID: NCT06303336 Recruiting - Clinical trials for Diplegic Spastic Cerebral Palsy

Effects OF NMES With and Without Dynamic Bracing on Spasticity and Movement Quality in CP

Start date: December 30, 2023
Phase: N/A
Study type: Interventional

The study aims at comparing Neuromuscular electrical Stimulation with and without dynamic bracing on spasticity and movement quality of lower limb in Children with Cerebral Palsy

NCT ID: NCT06303323 Recruiting - Clinical trials for Cardiovascular Diseases

Comparative Effectiveness of Qigong Exercise Versus Wu Dang Tai Chi Chuan in CVD Risk Individuals

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

To compare whether the Qigong exercise or Wu Dang Tai Chi Chuan will be effective in improving exercise capacity and reducing stress in CVD-risk individuals. Based on preliminary data, Qigong and Tai-Chi may help treat anxiety and depression symptoms in patients with chronic illnesses as well as in healthy adults. Without the need for specialized equipment, Qigong and Tai-Chi are both readily adjustable mind-body exercises that may be done whenever and wherever. For this reason, Qigong and TaiChi should be extensively encouraged as ways to enhance emotional wellbeing

NCT ID: NCT06303310 Recruiting - Vestibular Disorder Clinical Trials

Comparative Effects Of Gaze Stability Exercises And Optokinetic Exercises In Patients With Vestibular Hypofunction

Start date: February 20, 2024
Phase: N/A
Study type: Interventional

This randomized clinical trial will occur at Bahawal Victoria Hospital, Bahawalpur within 7 months after the approval of synopsis. The sample size for this trial will be 40 participants. Participants fulfilling the inclusion criteria will be recruited by using the convenience sampling randomly allocated into two groups by computer generator method. 20 participants will be assigned to Group A receiving gaze stability exercises and 20 to the Group B receiving optokinetic exercises, both alongside routine physical therapy. Each group will undergo 5 weekly sessions of treatment for 4 weeks.The assessment tools include Dizziness Handicap Inventory for dizziness; Mini-BESTest and modified-Clinical Test of Sensory Interaction of Balance for balance assessment while Vestibular Disorders Activities of Daily Living Scale for daily activities.

NCT ID: NCT06303297 Recruiting - Clinical trials for Postmenopausal Disorder

Effects of Reflexology and Generalized Stretching in Postmenopausal Females.

Start date: November 23, 2023
Phase: N/A
Study type: Interventional

To determine the combined Effects of reflexology and generalized stretching on insomnia, vasomotor symptoms and quality of life in postmenopausal females

NCT ID: NCT06303271 Recruiting - Clinical trials for Vestibular Hypofunction

Transcutaneous Auricular Vagus Nerve Stimulation on Dizziness & Balance in Elderly Population

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

The objective of the study is to determine the effects of transcutaneous auricular vagus nerve stimulation on dizziness and balance on elderly population with unilateral vestibular hypofunction. Patients will be divided into experimental and control group. Randomized participants will be allocated into control and experimental group. Intervention Group A received Vagus Nerve Stimulation (VNS) and Caw Thorne Cooksey exercise while Group group B received Caw Thorne Cooksey exercise only. Both groups received intervention of 30 minutes daily for 4 weeks (16 sessions). Assessment was done at the baseline, after 2 weeks and after 4 weeks

NCT ID: NCT06303258 Recruiting - Low Back Pain Clinical Trials

Generalized Versus Core Stabilization Antenatal Exercises For Lumbopelvic Pain

Start date: March 4, 2024
Phase: N/A
Study type: Interventional

Core stability training has gained popularity as a fitness trend and is now being used in rehabilitation programs as well the patient adherence to this intervention has been low due to its complex nature, particularly pregnant females .Limited literature is available to present the effect of core stabilization exercises in comparison to the other handful simplified techniques and exercises This study compares two interventions for this particular condition to identify a feasible and enjoyable therapeutic intervention for the pregnant women who suffer Lumbopelvic Pain.

NCT ID: NCT06303245 Recruiting - Clinical trials for Cesarean Section; Complications, Wound, Dehiscence

Effects of Abdominal Binders and TENS on Puerperium Period After Cesarean Section

Start date: February 23, 2023
Phase: N/A
Study type: Interventional

To determine the combined effects of abdominal binders and TENS on post-operative pain, distress and constipation in puerperium period after cesarean section

NCT ID: NCT06303232 Recruiting - Clinical trials for Postpartum Complication

Effects of Manual Lymphatic Drainage and Therapeutic Ultrasound on Breast Engorgement

Start date: February 23, 2023
Phase: N/A
Study type: Interventional

To find the combined effects of the manual lymphatic drainage with therapeutic ultrasound on breast engorgement, pain and self-efficacy in post - partum women.

NCT ID: NCT06303219 Recruiting - Clinical trials for Polycystic Ovarian Syndrome

Effects of Traditional Moderate Intensity Training and High Intensity Interval Training in Polycystic Ovarian Syndrome

Start date: November 23, 2023
Phase: N/A
Study type: Interventional

To determine the comparative effects of traditional moderate intensity training and high intensity interval training on Anxiety, fatigue and Quality of Life in females with polycystic ovarian syndrome

NCT ID: NCT06303050 Recruiting - Clinical trials for Stroke, Cardiovascular

Additional Effects of Mental Imagery Along With Task Oriented Training on Kinesiophobia in Patients With Stroke

Start date: December 7, 2023
Phase: N/A
Study type: Interventional

The objective of this study to determine the effect of mental imagery and task oriented training on Kinesiophobia in stroke patients. And to determine the association of Kinesiophobia with gait and balance in stroke patients. Patients will be divided into experimental and control group. Randomized participants will be allocated into control and experimental group. The experimental group will receive 20 minutes of MI training followed by 25 minutes of TOT for a total of 45 minutes, 5 days per week for 6 weeks.