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NCT ID: NCT06181461 Recruiting - Adhesive Capsulitis Clinical Trials

Gong's Versus Kaltenborn Mobilization on Pain, Range of Motion and Function in Adhesive Capsulitis

Start date: September 28, 2023
Phase: N/A
Study type: Interventional

The study will be a Randomized Clinical Trial set to take place at the Department of Physical Therapy, University of Lahore Teaching Hospital, Defence Road, Lahore. It is projected to span 9 months, beginning after the approval of the synopsis. The calculated sample size, utilizing Visual Analogue Scale as an outcome measure with a 20% dropout consideration, will be 34 in each group. Ethical approval from the Research Ethical Committee will be sought, and participant referrals will be facilitated by orthopedic physicians. Eligibility screening will be carried out, and willing participants will be randomized into Experimental and Comparative groups using a lottery method. The study will maintain single-blinding, with assessors remaining unaware of group allocation.

NCT ID: NCT06178705 Active, not recruiting - Clinical trials for Parent-Child Relations

Parenting Program for Parents of Children With Emotional and Behavioral Issues: A Randomized Control Trial

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

The main objectives of the study are: 1. To find out the effectiveness of Helpful Parenting Program (HPP) for psychological functioning of children's parent having behavioral and emotional issues. 2. To decrease psychological distress among children's parent having behavioral and emotional issues.

NCT ID: NCT06177223 Active, not recruiting - Clinical trials for Cognitive Behavioral Therapy

Cognitive Behavioral Therapy for Post-Traumatic Stress Disorder

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

The current study is designed to measure the role of cognitive behavior therapy with PTSD patients. There are following objectives of this current study, such as 1. To examine the efficacy of CBT to overcome the severity level of PTSD and associated psychiatric problems. 2. To change negative thought patterns and dysfunctional cognition into functional thoughts and beliefs. 3. To build up social support, enhance the quality of life and refine mental health among patients with PTSD. 4. To check outs the association of PTSD with depression, intimate partner violence stigma, marital adjustment, and abuse. 5. This study would examine the efficacy of CBT to treat the severity of PTSD and associated problems (i.e. depressive symptoms, adjustment problems & discrimination) among women victims of domestic violence in shelter homes

NCT ID: NCT06176755 Completed - Down's Syndrome Clinical Trials

Treadmill Training With and Without Weighted Ankle Cuffs on Gait Parameters

Start date: October 26, 2023
Phase: N/A
Study type: Interventional

Down syndrome is a condition in which a person has an extra chromosome. Chromosomes are small "packages" of genes in the body. Down syndrome (DS), also known as trisomy 21, is caused by the presence of all or part of a third copy of chromosome 21. It is named after John Langdon Down, the British physician who described the syndrome for the first time in 1866.Down syndrome remains the most common chromosomal condition diagnosed in the United States. Current study will be randomized controlled trial. Study will be approved by ethical committee. After that informed consent will be taken and patients will be included in the study based on the inclusion criteria. Sampling technique will be simple random sampling the calculated sample sizes will be 25 in each group. All participants will be divided in two groups. One group will receive treadmill training with Weighted Ankle Cuffs and second group will receive treadmill training only. Conventional therapy will be given to both groups which include isometric, strengthening exercise and trunk exercise. The exercise was given for 10 repetitions/session. Infants will receive the treadmill training protocol about 6 min/day, 4 day/week at a belt speed of 0.18m/sec. After taking informed consent baseline measurement will be taken through gait assessment rating scale and Berg balance scale for balance and Gait parameters respectively. Data will be collected before treatment and after 6 weeks. Treatment session will be performed for 1 hour per day, 4 days a week for total of 6 weeks. The difference in improvement before and after 4th weeks will be noted and compared through SPSS 26.0.

NCT ID: NCT06176742 Recruiting - Asthma Clinical Trials

Comparative Effects of ACBT and Bubble Positive Expiratory Pressure Device in Asthmatic Patients

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

The study gap is that in previous studies the effects of bubble-PEP in different diseases have been studied but it's never been studied in asthmatic patients, so the reason behind this study is to see effects of bubble-PEP in Asthmatic Patients.

NCT ID: NCT06175195 Active, not recruiting - Psychoeducation Clinical Trials

Psychoeducational Program for Cancer Patients.

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

The main objective of the study are: 1. To explore the effectiveness of psychoeducation program for cancer patients who refuse treatment because of irrational fears and anxieties. 2. To explore the effectiveness of psychoeducation program for cancer patients who have negative attitudes, and low motivation toward treatment which causes depression and affects the quality of life.

NCT ID: NCT06174909 Completed - Pain Clinical Trials

In Vivo Comparative Study of Calcium Hydroxide and Triple Antibiotic Paste in Intracanal Medicament in Emergency Pain Reduction

Start date: November 1, 2022
Phase: N/A
Study type: Interventional

Interappointment pain is a universal concern for clinician and patients alike which remain a significant challenge for dentalprofessional.The purpose of this study was to evaluate the effects of calcium hydroxide, and triple antibiotic paste as intra-canal medicaments in emergency pain reduction in patients undergoing endodontic treatment .

NCT ID: NCT06174584 Completed - Rectal Prolapse Clinical Trials

Comparison of Cow Milk and 15% Hypertonic Saline in the Treatment of Rectal Prolapse in Children

Start date: February 1, 2021
Phase: Early Phase 1
Study type: Interventional

To see the outcome of results of Cow Milk & Hypertonic Saline in the treatment of Rectal Prolapse in Children

NCT ID: NCT06173856 Completed - Clinical trials for Hyperbilirubinemia, Neonatal

Effectiveness of Phototherapy With and Without Probiotics

Start date: January 10, 2022
Phase: N/A
Study type: Interventional

Raised serum bilirubin levels can cause kernicterus and premature infants are at increased risk due to metabolic immaturity. The standard treatment for neonatal jaundice is phototherapy but probiotics along with it can reduce the duration of phototherapy and hospitalization stay, secondarily can reduce the risk of nosocomial infection.

NCT ID: NCT06173583 Completed - Clinical trials for Postoperative Complications

ARISCAT and LAS VEGUS Risk Scores for Predicting Postoperative Pulmonary Complications After Cardiac Surgery

Start date: February 14, 2020
Phase:
Study type: Observational

The goal of this observational study is to compare the, ARISCAT and LAS VEGUS scales, for predicting postoperative pulmonary complications in patients undergoing cardiac surgery. The study aims to compare the diagnostic accuracies of the two risk prediction scores in predicting postoperative pulmonary complications.