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NCT ID: NCT06190977 Not yet recruiting - Clinical trials for Total Knee Replacement

Effects of OEP on Rehabilitation Outcomes on TKR Patients

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

The aim of this research is to assess the effects of the Otago Exercise Program on Rehabilitation outcomes of balance strength and functional outcomes of post Total Knee Replacement patients. A randomized controlled trial that will include a total of 44 participants divided into two groups control and experimental. The experimental group will receive the Otago Exercise Program for four weeks, three times per week for forty to forty-five minutes. The control group will receive general TKR protocol for four weeks, three times per week for 30 minutes. Data collected will be analyzed through SPSS 25.

NCT ID: NCT06190418 Recruiting - Cerebral Palsy Clinical Trials

Loaded Vs Unloaded Sit to Stand Strengthening Exercises in Children With Cerebral Palsy

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

Cerebral palsy(CP) is non-progressive disorder, undergo mishap to the developing brain and it affect a person's ability to move and maintain balance and posture. Old name of CP is "Little's disease". Cerebral means having to do with the brain. Palsy means weakness or problems with using the muscles. In Spastic diplegic, muscle stiffness is mainly in the legs, with the arms less affected or not affected at all. The most common cause of spastic diplegia is Periventricular leukomalacia, more commonly known as neonatal asphyxia or infant hypoxia-a sudden in-womb shortage of oxygen-delivery through the umbilical cord. Strength exercise is any activity that makes your muscles work harder than usual. The significance of this study is that it will define whether loaded or unloaded sit to stand strengthening exercises have good effect on muscle strength and energy expenditure in diaplegic CP. This will be a randomized clinical trial, data will be collected from District Head Quarter DHQ hafizabad. Study will be conducted on 32 patients. Inclusion criteria of this study is spastic diplegic CP children with age between 6 to 12 years, with GMFCS level 1 and 2 and those who are able to stand up from chair independently and maintain standing for more than 5 seconds without falling will be included.Diplegic CP children who had not received any strengthening exercise program in past 3 months and those less than 20 degrees limitation in passive range of motion in hip flexion will be included. Those diplegic spastic CP who have orthopedic intervention such as selective dorsal rhizotomy or botolinum toxin injection to lower extremities within past six months and orthopedic conditions or medical problems that prevented children from participating in exercises will be excluded. Group A will be provided with loaded sit to stand strengthening exercises. 1 repetition maximum(1-RM) will be used as loaded sit to stand test. Group B will be provided with unloaded sit to stand strengthening exercises. Pre and post session lower limb functional strength will be measured by performing functional strength tests while lower limb muscular strength will be measured via modified sphygmomanometer and physiological cost index will be measured to rule out energy expenditure.

NCT ID: NCT06190106 Active, not recruiting - Clinical trials for Experiences of Psychitherapeutic Outcomes in Women Victims of Domestic Violence

Experiences of Psychotherapeutic Outcomes in Women Victims of Domestic Violence

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

The main objectives of the study are: 1. To explore the experience of undergoing psychotherapy of women victims of domestic violence. 2. To explore the effects of undergoing psychotherapy among women with victims of domestic violence.

NCT ID: NCT06189534 Active, not recruiting - Clinical trials for Cognitive Behavior Therapy for Social Media Addiction

Cognitive Behavior Therapy for Social Media Addiction, Insomnia, and Family Relationship Among Individuals With Social Media Addiction: A Randomized Control Tria

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

Objectives This study is designed to investigate the following objectives To manage the social media addiction in order to improve lifestyle, attitude and family relations of the individuals and explore related psychological problems which can arise because of this addiction. To explore the effectiveness of cognitive behaviour therapy (CBT) in the management of social media addiction in individuals which is decreasing the health of their lifestyle, attitude and family bonding. To explain how abusive use of social media can increase the risk of psychological and behavioural problems.

NCT ID: NCT06189469 Completed - Clinical trials for Urinary Incontinence

Reliability and Validity of Urdu Version of the King's Health Questionnaire

Start date: May 30, 2021
Phase:
Study type: Observational

This study is aimed to translate King's Health Questionnaire into Urdu language and to test its reliability and validity among Pakistani women with urinary incontinence.

NCT ID: NCT06189196 Recruiting - COPD Clinical Trials

Effects of Blow Bottle Verses ACBTs Technique in Patients of Chronic Obstructive Pulmonary Disease

Start date: August 18, 2023
Phase: N/A
Study type: Interventional

Chronic obstructive pulmonary disease is a common disease worldwide. Pulmonary rehabilitation is an important part to decrease the complications of COPD. Blow bottle technique is an economical and subjective technique promote the lung expansion, as compare to ACBTs. It used to treat the different complications in COPD patients and also decrease the dependency of patient. To find the comparative effects of blow bottle and active cycle of breathing on sputum diary, oxygen saturation, pulmonary function and quality of life among the patients of chronic bronchitis. A randomized clinical trial will be conducted at Gulab Devi hospital Lahore. Through convenient sampling technique on 56 patients, allocated through simple random sampling through computer generated technique into group A and Group B. Group A will be treated with blow bottle technique and group B will be treated by with ACBTs. Pretreatment values will be recorded for BCSS for sputum, pulse oximeter, pulmonary function test and st. George for quality of life will be assessed before and after 8 weeks of the treatment. Data will be analyzed using SPSS software version 25. After assessing normality of data by Shapiro-Wilk test, it will be decided either parametric or non-parametric test will be use within a group or between two groups.

NCT ID: NCT06188728 Completed - Metabolic Disease Clinical Trials

Husk Fiber Intervention on Metabolic Health of Centrally Obese School Teachers

Start date: September 7, 2020
Phase: N/A
Study type: Interventional

A group of 120 school teachers (male=60, female=60) was divided into four subgroups for sixteen weeks of an interventional study. One group was kept in control while the other three groups were assigned intervention. One group was assigned intervention of lifestyle modification (LSM), the other group assigned the intervention of 5 gm psyllium husk fiber (PSH) two times a day, and the third group assigned the combined intervention of LSM & PSH. Each group comprised of 30 subjects with equal gender bifurcation (15 male and 15 female).

NCT ID: NCT06187298 Completed - Clinical trials for Irritable Bowel Syndrome

Effect of Oral Combined Berberine and Curcumin Pharmacological Therapy on IBS

Start date: August 25, 2020
Phase:
Study type: Observational

Irritable bowel syndrome (IBS) is a prevalent, chronic functional gastrointestinal (GI) disorder, characterized by recurrent abdominal discomfort (pain) associated with altered bowel movements. IBS has a considerable negative impact on people's quality of life (QoL). There is currently no specific treatment available for IBS; most of the therapeutic management is symptomatic. Reported evidence suggest that BBR and CUR can alleviate symptoms of IBS through their multiple pharmacological effects including preventing stress-induced intestinal inflammation and visceral hypersensitivity, reducing bowel motility, and regulating intestinal permeability, gut microme and gut-brain axis.

NCT ID: NCT06182826 Recruiting - Low Back Pain Clinical Trials

Effect of Core Engagement Exercises and Routine Exercise Therapy on Low Back Pain in Middle School Children

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

Low back pain is defined as the region of pain between the lower ribs and hips. Low back pain with respect to middle school children corresponds to the age where children and adolescents go to school for longer periods of time, having heavy bags, assuming poor postures while sitting for prolonged hours. Poor posture, prolonged sitting and lack of physical activity results in back pain that leads to poor performance in school as well as attendance.

NCT ID: NCT06182813 Recruiting - Clinical trials for Binaural Auditory Beats ,Hand-eye Coordination

The Effect of Binaural Auditory Beats on Hand-Eye Coordination in Adult Population

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

This research will deduce the effect of binaural auditory beats on Hand-Eye coordination and will further explore the connection between auditory binaural beats and potential health benefits whilst helping to raise awareness about the potential health benefits of binaural auditor beats among young adults. The purpose of the study is to determine the effect of binaural auditory beats on hand-eye coordination in adult population. This study will assess the effect of a beta acoustic beats with resultant frequency of 25 Hz and carrier frequencies of 385Hz in left ear and 410Hz β-acoustic frequency in corresponding right ear at the same time, The difference of magnitude of these two signals will provide the certain perceived wave frequency. Each individual will be exposed to either beta auditory beats or white noise according to the group allotted.