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Health, Subjective clinical trials

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NCT ID: NCT04649814 Completed - Clinical trials for Spinal Cord Injuries

Finnish Spinal Cord Injury Study (FinSCI)

FinSCI
Start date: February 1, 2019
Phase:
Study type: Observational [Patient Registry]

The purpose of the Finnish Spinal Cord Injury Study (FinSCI) is to identify factors related to the health and functioning of people with spinal cord injury (SCI), their challenges with accessibility and how such factors are interconnected. The International Classification of Functioning, Disability and Health (ICF) is used in the study as a structured framework. The study participants will be recruited from three SCI outpatient clinics, which together are responsible for the life-time care of the SCI population in Finland. Mixed methods are used including a questionnaire and interviews. The survey will be formed from patient-reported instruments; SCI-specified Spinal Cord Injury Secondary Condition Scale, Spinal Cord Independence Measure, Nottwil Environmental Factors Inventory Short Form and selected items of the generic instruments of Patient-Reported Outcomes Measurement Information System and National study of health, well-being and service. The survey covers 51 ICF categories. The study results can help develop care and rehabilitation policies with SCI, the planning of training models and information provided to various parties involved.

NCT ID: NCT04648748 Completed - Health, Subjective Clinical Trials

Normative Data of Hand Grip Strength in Healthy Adult Pakistani Population

Start date: November 10, 2020
Phase:
Study type: Observational

Normative data values of handgrip strength not only describes hand normality but is also used as an objective assessor of upper extremities damages for Occupational Therapy and Physical Therapy interventions. Published normative data of different populations are widely available and can be used as reference. It is evident from different researches that various anthropometric variables such as age, gender, ethnicity, nutritional status, shoulder circumference & Body Mass Index(BMI), type of occupation and hand dominance of any population influence the hand muscles grip strength. Whereas, some literature shows disparity over the correlation between hand grip strength and BMI, several researchers claiming a positive relationship between BMI and grip strength in all ages of both genders, while other indicates no relationship. Approximately 3000 volunteers will be recruited from the staff, medical students, and visitors of different medical college & universities of Lahore. Subjects will be excluded if they had a history of upper-limb injury or deformity, or related health conditions. Socioeconomic background, general health, and lifestyle of the subjects will be assessed using a standard questionnaire. Weight, height & APM thickness will be measured prior to testing. Correlation between Hand Grip Strength and age, weight, height, body mass index (BMI), and Adductor Polices Muscle Thickness (APMT) will be measured. Multiple linear regression analysis will be used to adjust for the effects of other variables and to identify those independently associated with Hand grip strength. All the analysis will be carried out on SPSS v 25.

NCT ID: NCT04642235 Completed - Health Behavior Clinical Trials

Nature and Well-Being Project

Start date: April 12, 2021
Phase: N/A
Study type: Interventional

The investigators pilot test two intervention strategies to increase green space use- place-based and person-based, as well as evaluate the dose-response relationship between green space use and health.

NCT ID: NCT04639102 Completed - Clinical trials for Health Care Utilization

Practical Alternative to Hospitalization

PATH
Start date: February 9, 2021
Phase: N/A
Study type: Interventional

The investigators test the PATH program to evaluate whether the program allows patients to spend more days at home in comparison to patients who receive regular care. The program will involve patients from Penn Presbyterian Medical Center with a set of diagnoses and will provide patients with enhanced services upon discharge from the emergency department.

NCT ID: NCT04616716 Completed - Health, Subjective Clinical Trials

A Food Effect Study of FMTN on Healthy Chinese Adult Subjects

Start date: May 6, 2020
Phase: Phase 1
Study type: Interventional

The primary objective of the study was to assess the effect of high-fat and low-fat meal on the pharmacokinetics of FMTN in Chinese adult healthy subjects. The secondary objective of the study was to assess the safety of FMTN administered in adult healthy subjects.

NCT ID: NCT04555954 Completed - Healthy Clinical Trials

Determining the Physical Activity Level of Healthy Adults During Pandemic

Start date: April 11, 2020
Phase:
Study type: Observational

Abstract Background: With Covid-19 pandemic, online education, remote and flexible working were introduced. Thus the process of stay-at-home began. Purpose: The aim of the study is to determine level of physical activity of healthy adults in the pandemic process. Methods: This is a descriptive survey study which was applied via internet. The physical activity level was evaluated with International Physical Activity Questionnaire Short Form. Healthy adults aged 18-65 years who live in Turkey were included in the study.

NCT ID: NCT04499560 Completed - Inflammation Clinical Trials

The Effects of a Nutrition Supplement on Health Related Quality of Life

Start date: August 3, 2020
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the health related benefits of a superfoods nutrition supplement on health related quality of life.

NCT ID: NCT04455100 Completed - Health, Subjective Clinical Trials

A Phase I Study of SHR1459 in Healthy Subjects

Start date: July 17, 2020
Phase: Phase 1
Study type: Interventional

Following a 10-hour overnight fast, subjects will be administered one dose of SHR1459 orally with 240 mL of ambient temperature water on Day 1. D2-D3 was the cleaning period. Itraconazole will be administered orally 200 mg/time/day form D4 to D8 after meal. On D7 following a 10-hour overnight fast, subjects will be administered SHR1459 and itraconazole 200 mg with 240 mL of ambient temperature water.

NCT ID: NCT04087525 Completed - Health, Subjective Clinical Trials

A Study to Evaluate the Pharmacokinetics and Safety of HIP1701 in Healthy Subjects

Start date: October 23, 2018
Phase: Phase 1
Study type: Interventional

An open-label, randomized, single-dose crossover study to evaluate the pharmacokinetics and safety of HIP1701 in healthy subjects.

NCT ID: NCT04081857 Completed - Health, Subjective Clinical Trials

A Study to Evaluate the Pharmacokinetics and Safety of HCP1704 in Healthy Subjects

Start date: June 3, 2019
Phase: Phase 1
Study type: Interventional

An open-label, randomized, single-dose crossover study to evaluate the pharmacokinetics and safety of HCP1704 in healthy subjects.