The Treatment of Creative Blocks: A Comparison of Waking Imagery, Hypnotic Dream, and Rational Discussion Techniques

1981 ◽  
Vol 1 (1) ◽  
pp. 89-109 ◽  
Author(s):  
Michael V. Barrios ◽  
Jerome L. Singer
Keyword(s):  
Attentional Control ◽  
Positive Change ◽  
Imagery Condition ◽  
Public And Private ◽  
Induction Procedure ◽  
Hypnotic Induction ◽  
The Status ◽  
Task Irrelevant ◽  
And Task

Forty-eight volunteers reporting creative blocks in relation to artistic, literary, scientific, or professional projects, were randomly assigned to one of four conditions: (1) Waking Imagery, (2) Hypnotic Dream, (3) Rational Discussion, or (4) Control. In the Waking Imagery condition, participants engaged in ten directed imagination exercises, and subsequently generated three waking fantasies related to their creative projects. In the Hypnotic Dream condition, participants were exposed to a hypnotic induction procedure, and subsequently produced three hypnotic dreams related to their creative projects. The Rational Discussion condition involved a highly focused and logical collaborative examination of participants' creative projects, in which distractions and task-irrelevant thoughts were avoided. The Control condition simply involved encouraging participants, in a nondirective fashion, to discuss their projects. Follow-up a week after conclusion of treatment involved a rating by participants of Satisfaction and an account of changes, if any, in the creative block. Results suggest that the Waking Imagery and Hypnotic Dream conditions were most effective in promoting resolution of creative blocks. An examination of a number of possible predispositional features reveals that, overall, individuals with good attentional control and with low pretreatment levels of dysphoric daydreaming (e.g., guilty or hostile fantasies) were most likely to demonstrate a positive change in the status of their block. Intercorrelations between predispositional measures such as daydreaming styles, Public and Private Self-Consciousness, Absorption, and Hypnotic Susceptibility were also considered.

scholarly journals Top-down attentional control in spatially coincident stimuli enhances activity in both task-relevant and task-irrelevant regions of cortex

2009 ◽  
Vol 197 (1) ◽  
pp. 186-197 ◽  
Author(s):  
K ERICKSON ◽  
R PRAKASH ◽  
J KIM ◽  
B SUTTON ◽  
S COLCOMBE ◽  
...  
Keyword(s):  
Attentional Control ◽  
Top Down ◽  
Task Irrelevant ◽  
And Task

Status of Histopathology Services In Ethiopia

2020 ◽  
Vol 154 (Supplement_1) ◽  
pp. S120-S120
Author(s):  
G O Yeabyo
Keyword(s):  
Addis Ababa ◽  
Public Health Problem ◽  
Cross Sectional Study ◽  
Sectional Study ◽  
Cross Sectional ◽  
The Status ◽  
Prevention Of Cancer ◽  
Great Public Health ◽  
Cancer Diseases

Abstract Introduction/Objective Cancer is one of a great public health problem in developing countries like Ethiopia and scarcity of histopathology laboratory is another burden for diagnosis and follow up of cancer diseases. The main purpose of this study is to evaluate the accessibility of histopathology services in Ethiopia. Methods Cross sectional study design were used to analyze the status of histopathology services in Ethiopia. Results There are 13 histopathology laboratories in the nation and a survey was conducted at these institutions. Out of these 13 Histopathology services seven are located in the capital, Addis Ababa and six found out of the capital located in four different regions. About 40,239,100 habitants have no histopathology service around their catchment area. Conclusion There are very limited histopathology laboratories, as a result diagnosis and prevention of cancer diseases are inadequate throughout the country.

TRENDS IN HEALTH LEGISLATION AND ADMINISTRATION

PEDIATRICS ◽  
1948 ◽  
Vol 2 (3) ◽  
pp. 357-360
Keyword(s):  
Child Health ◽  
Parent Education ◽  
Maternal And Child Health ◽  
Good Life ◽  
Child Life ◽  
Human Beings ◽  
Public And Private ◽  
The People ◽  
The Status ◽  
And Child Health

TWO months ago when some of the salient features of the National Health Assembly were reviewed in this column (July issue), the report of the Maternal and Child Health Section was reserved for more complete presentation. This Section report is far too bulky to be quoted fully here. It includes first a factual summary of the present status of maternal and child health under the heading: "Where are we now in Maternal and Child Health?" Sub-committees, each of which submitted separate reports, were appointed to consider the following topics: 1. Training of personnel 2. Health of the School Age Child 3. Parent Education 4. Program to Raise Standards of Maternity, Newborn, and Pediatric Hospital Care 5. Research Program in Child Life 6. Care of the Handicapped, Including Prevention of Accidents Because other sections of the Assembly considered nutrition, dental care, environmental sanitation, mental hygiene and the chronic diseases common in childhood, these important factors were not considered in detail by the Maternal and Child Health Section. The most important part of the report is a summary entitled: "Goals for Maternal and Child Health." This statement includes the Sub-committee recommendations which were agreed upon as the most significant. This summary is therefore quoted in full as follows: Goals for Maternal and Child Health Whenever stock is taken of achievements designed to increase the chances of a good life and to improve the conditions of living, the people turn to examine the status of public and private action in behalf of children and to assess the extent and quality of care provided. This is natural because we recognize that the good life for mankind and world peace lies in the health and vigor of children, in their capacity to learn, in their ability to grow as thinking, reasoning human beings, and to develop from infancy through childhood and youth until they reach adulthood as fully mature persons, secure in their ability to take their places as citizens and as parents.

Dedicated clinical trial tissue tracking database to improve turn-around time at high-volume center.

2021 ◽  
Vol 39 (15_suppl) ◽  
pp. 1543-1543
Author(s):  
Peter Blankenship ◽  
David DeLaRosa ◽  
Marc Burris ◽  
Steven Cusson ◽  
Kayla Hendricks ◽  
...  
Keyword(s):  
Clinical Trial ◽  
Clinical Trials ◽  
Tissue Sample ◽  
High Volume ◽  
Trial Participation ◽  
Fresh Tissue ◽  
Oncology Clinical Trials ◽  
The Status ◽  
Unique Source

1543 Background: Tissue requirements in oncology clinical trials are increasingly complex due to prescreening protocols for patient selection and serial biopsies to understand molecular-level treatment effects. Novel solutions for tissue processing are necessary for timely tissue procurement. Based on these needs, we developed a Tissue Tracker (TT), a comprehensive database for study-related tissue tasks at our high-volume clinical trial center. Methods: In this Microsoft Access database, patients are assigned an ID within the TT that is associated with their name, medical record number, and study that follows their request to external users: pathology departments, clinical trial coordinators and data team members. To complete tasks in the TT, relevant information is required to update the status. Due to the high number of archival tissue requests from unique pathology labs, the TT has a “Follow-Up Dashboard” that organizes information needed to conduct follow-up on all archival samples with the status “Requested”. This results in an autogenerated email and pdf report sent to necessary teams. The TT also includes a kit inventory system and a real-time read only version formatted for interdepartmental communication, metric reporting, and other data-driven efforts. The primary outcome in this study was to evaluate our average turnaround time (ATAT: average time from request to shipment) for archival and fresh tissue samples before and after TT development. Results: Before implementing the TT, between March 2016 and March 2018, we processed 2676 archival requests from 235 unique source labs resulting in 2040 shipments with an ATAT of 19.29 days. We also processed 1099 fresh biopsies resulting in 944 shipments with an ATAT of 7.72 days. After TT implementation, between April 2018 and April 2020, we processed 2664 archival requests from 204 unique source labs resulting in 2506 shipments (+28.0%) with an ATAT of 14.78 days (-23.4%). During that same period, we processed 1795 fresh biopsies (+63.3%) resulting in 2006 shipments (+112.5%) with an ATAT of 6.85 days (-11.3%). Conclusions: Oncology clinical trials continue to evolve toward more extensive tissue requirements for prescreening and scientific exploration of on-treatment molecular profiling. Timely results are required to optimize patient trial participation. During the intervention period, our tissue sample volume and shipments increased, but the development and implementation of an automated tracking system allowed improvement in ATAT of both archival and fresh tissue. This automation not only improves end-user expectations and experiences for patients and trial sponsors but this allows our team to adapt to the increasing interest in tissue exploration.

Sign in / Sign up

Export Citation Format

Share Document