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NCT ID: NCT06079944 Recruiting - Clinical trials for Shoulder Impingement Syndrome

Effects of Progressive Resistance Training Combined With Traditional Physical Therapy in Patients With Shoulder Impingement Syndrome

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

A randomized control trial will be done on diagnosed Shoulder impingemnet patients with physical therapy screening in Fauji Foundation Hospital Rawalpindi. There is a growing demand on finding treatments which can be more beneficial and can be started early on in the treatment phase, nowadays. The purpose of the study is to determine the "effects of progressive resistance training combined with traditional physical therapy in patients with shoulder impingement syndrome" using the resistance band and multipulley system. The traditional physical therapy will include hot pack placed on shoulder and neck region for ten minutes, Transcutaneous electrical nerve stimular will be used and the electrodes will be placed on the desired area (shoulder complex) the intensity will be increased manually according to the capacity of the patient and the treatment time will be of 15 minutes, stretching exercises such as doorway stretch and foam roll supine stretch will be done in the hospital for first 3 weeks and the next 3 weeks will be for home exercises moving from 5 repetitions to 20 repetitions for a set of 3. stretch will be hold for 30 seconds

NCT ID: NCT06076408 Recruiting - Clinical trials for Lumbar Disc Herniation

Effects of SNAGS With and Without Pilates in Lumbar Disc Bulge Patients

Start date: October 3, 2023
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effects of Sustained Natural Apophyseal Glides with and without Pilates on pain, range of motion and disability in patients with lumbar Disc Bulge.

NCT ID: NCT06076278 Recruiting - Clinical trials for Osteoarthritis, Knee

Effects of Home Based Resistance Training as Compared to Supervised Resistance Training Exercise in the Management of Osteoarthritis.

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

Knee osteoarthritis is a degenerative pathology that is characterized by structural changes in the joint, such as joint space narrowing, thickening of the joint capsule, and cartilage degeneration that encourages friction between the bone surfaces and causes pain, which is thought to be a major symptom of knee osteoarthritis. Knee osteoarthritis (OA) treatment focuses on reducing pain while also enhancing function and quality of life by resistant training and Home-based exercise, a time-effective and practical treatment option for people with chronic conditions. As the past literature states that home based trainings are cost and time effective, However there is deficient evidence regarding effectiveness of home based strength training in case of knee osteoarthritis. More evidence is therefore needed in this regard.

NCT ID: NCT06074952 Recruiting - Color Stability Clinical Trials

Comparing the Color Stability of Acrylic Denture Teeth in Different Staining Solutions

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

The purpose of this (In Vitro Experimental Trial) is to assess (the color stability of acrylic denture teeth) in( different staining solutions) at (time intervals). The (acrylic denture) teeth will be immersed in (staining solutions) and the values will be recorded at (different time intervals). Three groups will be made: - Group A- Control group - Group B- Study group - Group C- Study group

NCT ID: NCT06074653 Recruiting - Muscle Tightness Clinical Trials

Effects of Mulligans BLR and CR on Hamstrings Flexibility in Office Workers

Start date: October 3, 2023
Phase: N/A
Study type: Interventional

The aim of this research is to compare the effect of mulligan bent leg raise and contract relax technique on hamstring flexibility in office workers with sedentary life styles.

NCT ID: NCT06074640 Recruiting - Heel Pain Syndrome Clinical Trials

Effects of PIR With and Without Dry Needling on Heel Pain

Start date: October 3, 2023
Phase: N/A
Study type: Interventional

The aim of this research will be to determine the effects of Post Isometric relaxation exercises with and without dry needling of triceps surae MTrPs on heel pain, ankle ROM and foot function in chronic heel pain patients. The sample size calculated for this study was 42. The subjects will be divided in two groups, 21 subjects in PIR with dry needling group and 21 in PIR without dry needling group. Study duration will be of 6 months. Sampling technique applied will be non probability convenience sampling technique. Only patients who are 20 - 40 years old, have NPRS score of heel pain above 3 and have MTrPs in any of the triceps surae muscle on initial inspection are included. Tools used in the study are Goniometer, NPRS scale and Foot function Index. Data will be analyzed through SPSS 23.

NCT ID: NCT06072469 Recruiting - Athletes Clinical Trials

Comparison of Shoulder Range of Motion and Isometric Strength Before and After a Single Badminton Match in Young Elite Badminton Players of Rawalpindi.

Start date: September 4, 2023
Phase:
Study type: Observational

The goal of this study is to compare the result of shoulder ranges of motion and isometric strength before and after a single badminton match in young elite badminton players of Rawalpindi. This is an observational study. The main questions it aims to answer is; Does the shoulder ranges of motion and isometric strength increases or decreases before and after a single badminton match. ROM and Isometric strength will be performed on the participants.

NCT ID: NCT06067945 Recruiting - Clinical trials for Evaluation of Marginal and Internal Fit of Metal Crowns

Comparison of Marginal Fit and Internal Adaptation in All-Metal Crowns: An In Vitro Experimental Trial

Start date: March 1, 2024
Phase:
Study type: Observational

The goal of this in vitro study is to compare the marginal fit and internal adaptation of all-metal crowns in polished crown preparations and non-polished crown preparations The main question it aims to answer is: are the non polished tooth preparations comparable to polished preparations? We will compare polish and non polish groups and see their effects on marginal fit and internal adaptation of all metal crown

NCT ID: NCT06065579 Recruiting - Clinical trials for Well-being, Emotional and Behavioral Problems, Adolescents

Efficacy of Well-Being Promotion Program for Management of Emotional and Behavioural Problems Among Adolescents

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

The objectives of the study are given as under; 1. To examine the efficacy of the Well-being Promotion Program in enhancing subjective well-being, positive affect, life satisfaction and reducing emotional /behavioral problems , negative affect among adolescents with emotional and behavioral problems. 2. To examine the differences in terms of subjective well-being, emotional / behavioral problems , positive / negative affect and life satisfaction between the treatment and control group after intervention. 3. To examine the differences in terms of subjective well-being, emotional / behavioral problems, positive / negative affect and life satisfaction in the intervention group at (T1) before and at (T2) after intervention.

NCT ID: NCT06064357 Recruiting - Clinical trials for Spastic Diplegia Cerebral Palsy

Comparison of Massage Therapy and Tissue Flossing Technique

Start date: March 21, 2023
Phase: N/A
Study type: Interventional

The purpose of the study is to compare massage therapy with tissue flossing technique in children with diplegic cerebral palsy. A randomized control trial would be conducted at helping hand for relief and development Quetta. The sample size is 56 calculated through G power. The participants would be divided into two interventional groups each having 28 participants. The study duration would be six weeks. Sampling technique applied would be convenient sampling for recruitment and group randomization via using envelop method. Tools used in this study are Goniometer, muscle length test and Functional Mobility scale. Data would be collected before and after 6 weeks of the application of interventions. Data analyzed through SPSS version 23.