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NCT ID: NCT01531634 Not yet recruiting - Clinical trials for Borderline Personality Disorder

Promoting Recovery Processes in Women With Borderline Personality Disorder Using a Dynamic Cognitive Intervention

Start date: n/a
Phase: N/A
Study type: Interventional

The field of psychiatric rehabilitation focuses on creating a personal narrative and developing coping strategies and environmental supports. The concept of recovery is person-centered and emphasizes the person's ability to change and to live meaningful life. The strengths approach has a central role in the recovery concept, emphasizing the person's abilities and potential. A preserved cognitive ability can be a significant strength in the recovery process. Research had shown growing support for the use of cognitive-behavioral approaches as the most effective therapy for people with borderline personality disorder, using structured interventions. A central focus in cognitive therapy is the change of maladaptive schemes. The dynamic-cognitive intervention (DCI) is based on the understanding of structural cognitive modifiability and suggests the use of mediated learning in order to enhance sense of competence and develop better psychological coping skills. The present study will focus on women diagnosed with borderline personality disorder, with normative cognitive ability seen as a strength as opposed to their emotional ability. This study will examine the effects of a Dynamic Cognitive Intervention on recovery measures and on symptoms severity. The study will include 30 women aged 18-45 years. Participants will be randomly assigned to an intervention group and a control group. All participants will be assessed before and after intervention using Recovery Assessment Scale, Hope Scale and The Brief Symptom Inventory. The intervention designed for this study is based on the principles of the Dynamic Cognitive Intervention. The intervention tools that will be used include: a. Instrumental Enrichment tools. b. life events analysis. c. Stories, lyrics and movie clips. d. Worksheets. The intervention encompasses 12 sessions of 1.5 hours, with a routine structure. The results are expected to contribute to the understanding of the impact of a dynamic cognitive intervention in women diagnosed with borderline personality disorder.

NCT ID: NCT01531127 Not yet recruiting - ADHD Clinical Trials

Executive Function in Learning in Children With Attention Deficit Hyperactivity Disorder (ADHD) Receiving Medical Treatment Alone Compared to Children Receiving Additional Treatment to Improve Learning Strategies

Start date: March 2012
Phase: N/A
Study type: Observational

The purpose of this study is to determine whether there is a difference in executive function in learning in children with ADHD receiving medical treatment alone to the executive function in children receiving, in addition to medical treatment in learning strategies.

NCT ID: NCT01530113 Not yet recruiting - Depression Clinical Trials

Childhood Sexual Abuse, Vaginismus and Labor Dystocia

CSA-V-LD
Start date: March 2012
Phase: N/A
Study type: Observational

The study aims to develop a theoretical model explicating the inter-relationships between Childhood Sexual Abuse (CSA), Partial Vaginismus (PV) and Labor Dystocia (LD), including their associations with Depression (D) as a mediating variable. The following research hypotheses will be tested: 1. CSA will serve as a risk factor for D, PV and LD. - pregnant women with a history of CSA will have higher levels of D compared to pregnant women without a history of CSA. - pregnant women with a history of CSA will have more PV compared to pregnant women without a history of CSA. - pregnant women with a history of CSA will have higher levels of LD compared to pregnant women without a history of CSA. 2. D will serve as a mediator between prenatal PV and LD. 3. PV will serve as a risk factor for LD. 4. postpartum PV will be affected by childbirth (LD vs. no LD) contingent on the level of D.

NCT ID: NCT01525784 Not yet recruiting - Clinical trials for Type 1 Diabetes Mellitus

Affect of RT-CGMS as Part of Clinical Care in Type 1 Diabetes Mellitus Patients

Start date: February 2012
Phase: N/A
Study type: Observational

The incidence of Type 1 Diabetes Mellitus is increasing annually, in all pediatric age groups, especially among infants and toddlers.However, only 30% of diabetic children manage to achieve and maintain glycated hemoglobin A1c (HbA1c) levels below 8%, although most are treated by intensive insulin therapy.Recently, devices for real-time continuous glucose monitoring (RT-CGMS) have been introduced to aid self management of glycemic control. These devices enable the patients to see the interstitial glucose levels continuously, the trends of decrement and increment, and to have alarms prior to a severe hypoglycemic episode . The RT-CGMS was approved in Israel for routine usage in the pediatric population, 0-18 years in 2011, indicated for those with recurrent hypoglycemic episodes. So, the aim of the investigators study is to examine prospectively the short and long term effect of the RT-CGMS routine usage, in daily routine life of the diabetic child.

NCT ID: NCT01524718 Not yet recruiting - Clinical trials for Fracture Neck of Femur

Internal Fixation of Hip Fractures Using Intraoperative Simultaneous Two Axis View

Start date: September 2012
Phase: N/A
Study type: Interventional

Hip fractures are one of the most frequent operated fractures procedures in orthopedics, with a world wide annual incidence of approximately 1.7 million. These fractures are associated with substantial morbidity and mortality. As populations age and life expectancy increases worldwide, the incidence of these fractures is likely to raise, expected to triple in the next 50 years. The use of fluoroscopy and resultant exposure to radiation, is an integral part of surgical procedures aiming to reduce and fixate the fractured femur. The risk of contracting cancer is significantly higher for an orthopedic surgeon as Hip surgery is a major slice of the total radiation dose. Optimal positioning and control of the imaging intensifier device may result in significant reduction of radiation dose and time and in substantial shortening of the procedure. The investigators hypothesis is that this technique would substantially shorten procedure time and reduce unnecessary radiation exposure for both the patient and the medical staff. Furthermore, by using this technique the investigators can eliminate the need for fluoroscopy technician during the surgery, as there is no need to alternate fluoroscopy views.

NCT ID: NCT01524419 Not yet recruiting - Mother (Person) Clinical Trials

Women's Involvement In Decision Making At Labor And Its Effect on Their Perceived Labor Process

Start date: March 2012
Phase: N/A
Study type: Observational

1. Increased women's involvement in decision making at labor process correlates with a positive perception of the labor process. 2. Increased maternal satisfaction with midwifery and gynecological care at labor correlates with a more positive perception of the labor process.

NCT ID: NCT01521221 Not yet recruiting - Clinical trials for Orthostatic Hypotension

Assessment of Hand-grip in the Prevention of Postural Orthostatic Hypotension

Start date: April 2012
Phase: Phase 1
Study type: Interventional

The study is aimed to assess the efficacy of hand-grip in preventing orthostatic hypotension in 20 patients diagnosed with autonomic failure. Five healthy subjects will be studied for comparison. The investigators will evaluate the subjects while on tilt table for 10 minutes and than while mounted from lying down to 70 degrees for additional 10 minutes. Blood pressure, heart rate and symptoms will be continuously measured. First study will evaluate the blood pressure changes. Second measure will include hand-grip maneuver 1 minute before the erect positon. Trans cranial Doppler will assess the intracranial blood flow during the position changes.

NCT ID: NCT01521052 Not yet recruiting - Depression Clinical Trials

Evaluation of the H-Coil Transcranial Magnetic Stimulation (TMS) Device - Safety and Feasibility Study for Treatment of Major Depressive Episode in the Elderly

Start date: January 2012
Phase: Phase 2
Study type: Interventional

Purpose: To evaluate the safety and anti-depressive response of the H1 Coil TMS Device in elderly patients suffering from major depressive episode. Twenty-seven (27) treatment resistance depressed-patients, 68 years of age and above, currently in a depressive episode.All subjects will receive prefrontal deep rTMS of H1 Coil (42 trains of 2 seconds, 10 Hz, with 20 seconds inter-train intervals, up to 120% of motor threshold), for 4 weeks, 5 days a week, overall 20 sessions.Safety and efficacy tests will be conducted before starting the trial (screening), once a week for the trial duration and one month following end of treatment.

NCT ID: NCT01520584 Not yet recruiting - Oligospermia Clinical Trials

Supplement Intake in Infertile Men;the Effect on Sperm Parameters,Fertilization Rate and Embryo Quality

Start date: January 2012
Phase: N/A
Study type: Interventional

The vitamin,minerals and amino acid supplementation for 3 months will improve the semen parameters,fertilization rate and embryo quality in subfertile men undergoing IVF treatment

NCT ID: NCT01519622 Not yet recruiting - Sick Elderly Clinical Trials

Impact of Disease on the Concept of End-of-life Decisions of the Elderly in the Community

Start date: February 2012
Phase: N/A
Study type: Observational

The purpose of this study is to determine the priorities of the elderly in the community about end-of-life decisions. To check the perception of the disease in the elderly in the community.