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NCT ID: NCT06230094 Recruiting - Sleep Clinical Trials

Effect of 8 Weeks Moderate & High Intensity Training on Cognitive Functions and Sleep of Female Students

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

this study aims to assess ther effectiveness of moderate & high intensity training on cognitive functions and sleep of female students

NCT ID: NCT06228950 Recruiting - Behavior Problem Clinical Trials

Mindfulness-Based Intervention for Emotional and Behavioural Problems of Students With Visual Impairment

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

Current study will be conducted on the Effectiveness of Mindfulness-Based Intervention for Emotional and Behavioural Problems of Students with Visual Impairment. Mindfulness-based Intervention that is Mindfulness-Based Stress Reduction (MBSR) will be used in the current study which is adapted and translated in Urdu language; the pilot trial of MBSR will be conducted after adaptation and translation. The present study will be conducted in two phases - First phase of the study would be a cross-sectional survey in which the researcher will conduct a baseline assessment to identify psychosocial predictors such as psychological distress, parental acceptance and rejection, social support, and mindfulness which are associated with the emotional and behavioural problems of students with visual impairment. Further emotional and behavioural problems of the students with visual impairment will identify. - The second phase of the research would be a Randomized Controlled Trial in which students with Visual Impairment who has scored high on psychosocial predictors and emotional & behavioural problems would be randomly assigned to intervention & control groups to get the MBSR training. After the successful training post-assessment would be conducted to check the efficacy of MBSR. - The current study will be conducted in Rawalpindi Islamabad after obtaining permission from the relevant authorities. - Data would be collected from the students with visual impairment and their respective parents.

NCT ID: NCT06227858 Recruiting - Clinical trials for Perimenopausal Disorder

Effects of a Standardised Saffron Extract Supplementation on Symptoms Associated With Perimenopause in Healthy Women

Start date: February 10, 2024
Phase: N/A
Study type: Interventional

The aim of the present study is to assess the effects of a normalised saffron extract supplementation, which is an extract of the flower Crocus sativus, on perimenopausal symptoms.

NCT ID: NCT06224790 Recruiting - Type 2 Diabetes Clinical Trials

Perfenidone in Type 2 Diabetic Patients With Diabetic Neuropathy

PenDaNt
Start date: March 10, 2024
Phase: Phase 4
Study type: Interventional

The purpose of this study is to determine the effectiveness & safety of pirfenidone in type 2 diabetic patients with diabetic nephropathy

NCT ID: NCT06212869 Recruiting - Migraine Clinical Trials

Green Light and Transcranial Direct Current Stimulation in Migraine Patients

Start date: January 18, 2024
Phase: N/A
Study type: Interventional

There is a lack of evidence on the clinical outcome of green light exposure, as it is the emerging, novel proposal of treatment. There are a lot of researches present with small sample size which should be done on large population. In last conducted studies, session numbers of the applied modality are less. There is no comparison of tDCS with green light for migraine. The literature suggested the neuromodulation influenced by these interventions that may result in reduction of migraine.

NCT ID: NCT06212856 Recruiting - Physical Fitness Clinical Trials

Effects of Plyometric Training on Physical Fitness and Technical Skills in Young Male Volleyball Players.

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

This study aims to find the effectiveness of Plyometric training on Physical fitness and Technical skills of young male volleyball players. Players would be taken from Prime Sports Academy and Prime Institute of Health Sciences, Islamabad and a well-designed Plyometric training plan will be implied on them for 8 weeks. After the time span, the result would be compared to check the effectiveness of the training plan.

NCT ID: NCT06212843 Recruiting - Injury Prevention Clinical Trials

Effect of 8 Week Plyometric Training on Injury Prevention in Domestic Cricket Players

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

The study aims to find the effectiveness of plyometric training on injury prevention of domestic cricket players. Players will be taken from Chakwal and a well designed plyometric plan will be implied on them for 8 weeks. After that the results will be compared with the other group who did not get any plyometric training to see the effectiveness of the treatment plan.

NCT ID: NCT06208293 Recruiting - Suicide Clinical Trials

Suicide Prevention Integration Into Task-shifted Mental Health Interventions

KPZ
Start date: May 13, 2024
Phase: N/A
Study type: Interventional

Investigators will conduct a pilot clinical trial to assess the feasibility and acceptability of implementing a Suicide Prevention Package (SuPP) within an existing task-shifted depression intervention in rural Pakistan. This pilot research lays the groundwork for a future project to scale a package for multi-level suicide prevention strategies that can be integrated into community based mental health programs, particularly targeting individuals living in low-resourced settings. As the model is designed to be easily adapted and integrated, investigators anticipate the findings will be valuable for all researchers looking to improve population health and mental health services in disadvantaged settings.

NCT ID: NCT06202664 Recruiting - Analgesia Clinical Trials

Opioid Free Anesthesia for Laparoscopic Cholecystectomy

Start date: January 15, 2024
Phase: Phase 4
Study type: Interventional

The goal of this interventional study is to check the efficacy of Erector Spinae block as Opioid Free Anesthesia for Laparoscopic Cholecystectomy. Laparoscopic Cholecystectomy is a commonly performed day care procedure. Being a day care procedure the anesthetic technique employed should provide adequate analgesia, allow early mobilization of patient and should mitigate nausea and vomiting which occurs quite frequently in this surgical population. If these goals are achieved patients can be discharged early from hospital setting and this leads to overall cost benefits.

NCT ID: NCT06202391 Recruiting - Scapular Dyskinesis Clinical Trials

Autogenic Inhibition Versus Reciprocal Inhibition Muscle Energy Techniques Effect on Swimming Performance on Swimmers With Scapular Dyskinesis

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

Swimming can cause shoulder pain due to scapular dyskinesis. Proper scapula movement is necessary for efficient swimming strokes and to avoid injury. Studying the effects of autogenic and reciprocal inhibition muscle energy techniques on swimmers with scapular dyskinesis can lead to effective interventions and reduce shoulder injuries