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NCT ID: NCT04319393 Completed - Ageism Clinical Trials

Cognitive Behavioral Therapy and Ageism

Start date: January 1, 2019
Phase: N/A
Study type: Interventional

Background: Healthcare settings must be a patient-friendly environment for the investigator's older adults who are in an imperative need for compassionate healthcare when approaching their later life. However, older adults until this moment are experiencing age discriminative acts by nurses who are supposed to act in favor of their patients. Ageism is not always a result of either negative attitudes or misconceptions toward older adults, but to the innate fear of death where nurses perceive older adults as a powerful reminder of death. Although cognitive-behavioral therapy (CBT) is well known for targeting psychological distresses, to date, no research has investigated its effectiveness in relieving nurses' death anxiety and ageism. This study examined the effectiveness of CBT to relieve nurses' death anxiety and ageism toward older adults. Methods: A randomized controlled trial was conducted during August 2019 in the university hospital. A total of 110 nurses selected through proportional stratified sampling and randomly assigned to the experimental and control groups. The intervention consisted of six two-hour training sessions delivered in five modules with the integration of different CBT exercises. The effect of CBT was assessed on measures of a series of validated questionnaires of study variables before and after the training sessions.

NCT ID: NCT04317768 Completed - Dental Caries Clinical Trials

Effect of Oral Health Education on Oral Health Status, Treatment Needs and Barriers to Care

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

Jordanian children have very poor oral hygiene parameters, and this is reflected as very high caries prevalence and poor gingival health conditions. This study will focus on children at social homes in the community in order to establish a baseline reference about their oral health status, treatment needs, and barriers to dental care. Also, to report the efficacy of oral health education using audio-visual aids and frequent motivation on oral health status, treatment needs and barriers to care among children at social homes in Jordan.

NCT ID: NCT04309890 Completed - Overactive Bladder Clinical Trials

Arabic Translation and Validation of the (Overactive Bladder Symptom Score) OABSS

Start date: February 1, 2019
Phase:
Study type: Observational

The English version of the Overactive Bladder Symptom Score (OABSS) questionnaire was translated to Arabic language. The questionnaire was validated by comparing the response to the questionnaire in a patient with Overactive Bladder (OAB) before and after providing treatment with antimuscarinics.

NCT ID: NCT04307784 Completed - Clinical trials for Vitamin D Deficiency

The Effects of Vitamin D3 Alone and in a Combination With Omega-3 on the Association of C-peptide With Glycemic Control

Start date: March 10, 2020
Phase: N/A
Study type: Interventional

The Effects of Vitamin D3 alone and in a combination with omega-3 on the association of C-peptide with glycemic control

NCT ID: NCT04288934 Completed - Clinical trials for Spinal Cord Injuries

Treatment of Spinal Cord Injuries With (AutoBM-MSCs)vs (WJ-MSCs).

Start date: August 15, 2017
Phase: Phase 1
Study type: Interventional

This study aims to assess and compare the safety and effectiveness of Autologous Bone Marrow-Derived MSCs (AutoBM-MSCs) in one group(group A) of SCI who are unlikely to be able to walk independently without treatment after 1 year of SCI, in the other group (group B) to assess the second group of Wharton Jelly derived mesenchymal stem cells ( WJ-MSCs) in the treatment of acute and subacute spinal cord injury (SCI) patients.

NCT ID: NCT04285528 Completed - Anesthesia Clinical Trials

Sedation and Analgesia Using PFK Versus General Anesthesia in Urological Procedures

Start date: April 17, 2019
Phase: N/A
Study type: Interventional

Anesthesia in urological surgeries might constitute a great challenge to anesthesiologists. Especially that a great proportion of these patients are elderly with a lot of comorbidities. This put these patients at the risk of developing medical adverse events after being anesthetized by general anesthesia. The aim of this study is to compare between intravenous sedation with analgesia versus general anesthesia in patients undergoing urological surgical procedures.

NCT ID: NCT04284644 Completed - Anesthesia Clinical Trials

Co-induction Technique Compared to Standard Inhalational and Intravenous Induction Techniques

Start date: May 1, 2016
Phase: N/A
Study type: Interventional

Co-induction technique refers to the use of a combination of medications to reach the desired therapeutic target. In the present study, the investigators examined the safety of a novel co-induction approach that relied on a simple timing and dosing alterations to the classical approaches of inhalational sevoflurane and propofol induction. The significance of this study is to find a reliable safe alternative method of induction that can provide optimal parameters,when compared to the classical methods of induction.

NCT ID: NCT04262765 Completed - Healthy Volunteers Clinical Trials

Drug-drug-interaction Study of Ramipril, Amlodipine and Atorvastatin

Start date: February 23, 2019
Phase: Phase 1
Study type: Interventional

Study to determine the potential pharmacokinetic interaction of ramipril (and ramiprilat), atorvastatin as atorvastatin calcium trihydrate and amlodipine as amlodipine besilate at steady state after a multiple oral administration and to monitor the safety of the co-administration of these drugs. This study aims to determine if the steady state study pharmacokinetic parameters of any of the given drugs and the tolerability is altered when administered concomitantly.

NCT ID: NCT04245046 Completed - Healthy Volunteers Clinical Trials

Drug-drug-interaction Study of Candesartan, Amlodipine and Atorvastatin

Start date: January 18, 2019
Phase: Phase 1
Study type: Interventional

Study to determine the potential pharmacokinetic interaction of candesartan cilexetil, atorvastatin as atorvastatin calcium trihydrate and amlodipine as amlodipine besilate at steady state after a multiple oral administration and to monitor the safety of the co-administration of these drugs. This study aims to determine if the steady state study pharmacokinetic parameters of any of the given drugs and the tolerability is altered when administered concomitantly.

NCT ID: NCT04237493 Completed - Clinical trials for Diabetes Mellitus, Type 2

Dosage Reduction and Acute Glycemic Complications in People With Type 2 Diabetes Who Fast During Ramadan

Start date: February 14, 2017
Phase: Phase 4
Study type: Interventional

Every lunar year, during the month of Ramadan, Muslims abstain from food and drink between dawn and nightfall. People with type 2 diabetes who fast during Ramadan are at an increased risk of acute glycemic complications. Our aim is to investigate the effect of dosage reduction of four glucose-lowering multidrug regimens on the incidence of acute glycemic complications in people with type 2 diabetes who fast during Ramadan.