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NCT ID: NCT06437730 Recruiting - Knee Osteoarthritis Clinical Trials

Comparison of INIT and Dry Needling on Trigger Points in Knee OA

Start date: October 12, 2023
Phase: N/A
Study type: Interventional

The purpose of the study is to compare the effects of Integrated Neuromuscular Inhibition Technique and Dry Needling on Functional Disability, Pain and Range of Motion. A randomized control trial will be conducted at Wah General Hospital Taxila. The sample size is 36 calculated through G-Power but I recruited 50. The participants were divided into two interventional groups each having 18 participants. Tools used in this study are Goniometer, NPRS, WOMAC, and Self structured Questionnaire. Data will be collected before and immediately after the application of interventions. Data will be analyzed through SPSS.

NCT ID: NCT06437704 Recruiting - Clinical trials for Mild Cognitive Impairment

Effects of Brain Training Games on Cognitive Function and Quality of Life in MCI

Start date: May 16, 2024
Phase: N/A
Study type: Interventional

The study aims to determine the effects of brain training games on cognitive function and Quality of life among older adults with MCI.

NCT ID: NCT06437613 Recruiting - Clinical trials for Hamstring Flexibility

"Effects of Passive Static Stretching of 30 Seconds Versus 60 Seconds on the Hamstring Flexibility in Adults With Hamstring Tightness.

Start date: July 15, 2023
Phase: N/A
Study type: Interventional

This study is a randomised controlled trial and the purpose of this study is to determine the effects of Passive Static Stretching of 30 seconds versus 60 seconds on the Hamstring Flexibility in adults with Hamstring Tightness. The study is conducted in Rehabilitation department of Fauji Foundation Hospital on the sample of 38 participants. Hamstring flexibility will be evaluated at the beginning by Active knee extension test. The subjects will be randomized into two group by sealed envelope method. Baseline assessment would be done by using tools of SLR and modified knee extension test and then final assessment will be done after 4 weeks.

NCT ID: NCT06437483 Recruiting - Neck Pain Clinical Trials

Effects of Sustained Natural Apophyseal Glides Combined With Kinesiotaping in Patients With Chronic Mechanical Neck Pain: A Randomised Controlled Trial

Start date: November 10, 2023
Phase: N/A
Study type: Interventional

This study is a randomized controlled trial and its purpose is to determine the combined effects of sustained natural apophyseal glides and kinesiotaping on pain, range of motion and neck disability in patients with chronic mechanical neck pain.

NCT ID: NCT06437327 Recruiting - Piriformis Syndrome Clinical Trials

Comparison of Effectiveness Between Active Release Technique and Hold Relax Technique in Patients With Piriformis Syndrome

Start date: July 15, 2023
Phase: N/A
Study type: Interventional

This study is a randomized controlled trial and the purpose of this study is to compare the effects between active release technique and hold relax technique in patients with Piriformis syndrome.

NCT ID: NCT06435052 Recruiting - Clinical trials for Post Traumatic Stress Disorder

Efficacy of Eye Movement Desensitization & Reprocessing vs Cognitive Behavioral Therapy in Post-Traumatic Stress and Comorbid Disorders in Pakistan

Start date: August 15, 2022
Phase: N/A
Study type: Interventional

This Randomized Controlled Trial will check the efficacy of Eye Movement Desensitization & Reprocessing vs Cognitive Behavioral Therapy in Post-Traumatic Stress and Comorbid Disorders in Pakistan

NCT ID: NCT06430892 Recruiting - Clinical trials for Myocardial Infarction, Acute

RAPID-POP a Randomized Controlled Trial

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

Efficacy of the Pressure Optimization Protocol (POP) versus Conventional Stent Deployment Strategy during Primary PCI: An Open Label Randomized Clinical Trial The investigators will compare conventional rapid stent inflation/deflation during primary PCI with higher pressure and prolonged duration of stent deployment Study Hypothesis: The POP in stent deployment is superior to the conventional stent deployment approach with a significantly higher achievement of the TIMI III flow, significantly lesser occurrence of slow flow/no-reflow, and significantly higher rate of ST-Segment resolution during primary PCI.

NCT ID: NCT06427616 Recruiting - Health Behavior Clinical Trials

Moderate Intensity Soleus Pushups Versus Sustained Soleus Pushups on Blood Glucose Level Among Young Population

Start date: October 1, 2023
Phase: N/A
Study type: Interventional

To determine that the short duration moderate intensity soleus push-ups will have a better effect on blood glucose level as compared to sustained soleus push-ups.

NCT ID: NCT06426914 Recruiting - Clinical trials for Post-cardiac Surgery

Clinical Pilates (CP) Exercises and Kinesiophobia in CABG

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

To determine Effect of Clinical Pilates (CP) exercises on kinesiophobia and post-operative cardiopulmonary parameters in CABG patients. Kinesiophobia may lead to patients' psychological fear of rehabilitation exercise, thereby refusing rehabilitation exercise, affecting the rehabilitation process of patients, resulting in disuse syndrome, depression, disability and other adverse consequences. Thus, this study is to be conducted to find out the effects Pilates exercises with cardiac rehabilitation for management of Kinesiophobia in post CABG patients.

NCT ID: NCT06426888 Recruiting - Clinical trials for Subacromial Impingement Syndrome

Comparison of Scapular Stabilization and Mobilizations in Sub Acromial Pain Syndrome

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

The aim of this research is to compare the effect Comparison of scapular stabilization exercises and scapular mobilizations on shoulder pain, scapular kinematics, disability and functional limitations in patients with sub acromial pain syndrome Randomized controlled trials done at District Head Quarters Mirpur AJK. The sample size was 36. The subjects were divided in two groups, 18 subjects in scapular mobilization exercise group and 18 in scapular mobilization exercise therapy group. Study duration was of 12 months. Sampling technique applied was non probability convenient sampling technique. Only 25-40 years old patient with unilateral shoulder pain lasting >6 weeks were included. Tools used in the study are NPRS, SPADI, WORC LSST and SAT.