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1.
Dtsch Med Wochenschr ; 145(16): 1133-1137, 2020 08.
Article in German | MEDLINE | ID: mdl-32791548

ABSTRACT

BACKGROUND: Immunosenescence leads to an increasing susceptibility to infections. Therefore, vaccination is an essential element of prevention. The recommendations of the permanent vaccination commission (STIKO), a committee at the Robert-Koch-Institute, affiliated to the German Government, are updated every year and include a particular section dealing with older adults. CURRENT DEVELOPMENTS: Immunosenescence reduces vaccine effectiveness. Thus, older adults and patients with multimorbidity are in need of more immunogenic vaccines. Cell culture derived quadrivalent influenza vaccine, trivalent adjuvanted vaccine and a high dose influenza vaccine show higher immune response in these groups. STIKO actually recommends an adjuvanted herpes zoster subunit vaccine to all adults in the age of 60 and above because of its vaccine effectiveness of 90 % in all age groups. The increasing travel activities of older adults require travel vaccination advice that takes into account travel destination as well as multimorbidity. Adjusted vaccination schedules and controlling of antibody titers have to be considered. OUTLOOK: New vaccines are under development, that are more immunogenic and therefore more effective (e. g. pneumococcal vaccine) or that prevent infections for which a vaccine was previously not available (e. g. norovirus vaccine).


Subject(s)
National Health Programs/legislation & jurisprudence , Vaccination/legislation & jurisprudence , Age Factors , Aged , Aged, 80 and over , Female , Germany , Humans , Immunization Schedule , Male , Middle Aged , Multimorbidity , Travel , Vaccination/methods , Voluntary Programs/legislation & jurisprudence
2.
Fed Regist ; 83(160): 40973-85, 2018 Aug 17.
Article in English | MEDLINE | ID: mdl-30192471

ABSTRACT

The Food and Drug Administration's (FDA, Agency, or we) Center for Devices and Radiological Health and Center for Biologics Evaluation and Research are announcing that the Agency is granting an alternative that permits manufacturer reporting of certain device malfunction medical device reports (MDRs) in summary form on a quarterly basis. We refer to this alternative as the "Voluntary Malfunction Summary Reporting Program." This voluntary program reflects goals for streamlining malfunction reporting outlined in the commitment letter agreed to by FDA and industry and submitted to Congress, as referenced in the Medical Device User Fee Amendments of 2017 (MDUFA IV Commitment Letter).


Subject(s)
Equipment Failure , Product Surveillance, Postmarketing , Voluntary Programs/legislation & jurisprudence , Equipment Safety , Equipment and Supplies/adverse effects , Humans , Public Health , United States , United States Food and Drug Administration/legislation & jurisprudence
3.
J Health Care Poor Underserved ; 29(1): 497-508, 2018.
Article in English | MEDLINE | ID: mdl-29503314

ABSTRACT

Voluntary paternity establishment was placed in birthing hospitals by an act of Congress, but little is known about how unmarried parents experience this process. This study presents reactions from 81 racially/ethnically diverse, low-income parents. A qualitative analysis of semi-structured interviews revealed three overall themes and six subthemes: (1) paternity establishment process [subthemes: variety of experiences, strong emotional experience, and poor timing]; (2) meaning of paternity establishment [subthemes: responsible fatherhood, symbol of commitment to child, and importance of the child knowing his father's identity]; and (3) paternity establishment decision-making. Many parents either did not recall receiving the requisite information or found it difficult to focus on technical materials immediately after childbirth. For parents, the symbolic value of the father's name on the birth certificate overrode other considerations. Parents' perspectives may help administrators of paternity establishment programs better tailor procedures and timing to the needs of unmarried parents.


Subject(s)
Parents/psychology , Paternity , Single Person/psychology , Birth Certificates , Cultural Diversity , Female , Hospitals , Humans , Male , Perception , Poverty , Pregnancy , Qualitative Research , Single Person/statistics & numerical data , United States , Voluntary Programs/legislation & jurisprudence
4.
Public Health Nutr ; 20(16): 3008-3018, 2017 Nov.
Article in English | MEDLINE | ID: mdl-28879830

ABSTRACT

OBJECTIVE: Fortification of food-grade (edible) salt with iodine is recommended as a safe, cost-effective and sustainable strategy for the prevention of iodine-deficiency disorders. The present paper examines the legislative framework for salt iodization in Asian countries. DESIGN: We reviewed salt iodization legislation in thirty-six countries in Asia and the Pacific. We obtained copies of existing and draft legislation for salt iodization from UNICEF country offices and the WHO's Global Database of Implementation of Nutrition Actions. We compiled legislation details by country and report on commonalities and gaps using a standardized form. The association between type of legislation and availability of iodized salt in households was assessed. RESULTS: We identified twenty-one countries with existing salt iodization legislation, of which eighteen were mandatory. A further nine countries have draft legislation. The majority of countries with draft and existing legislation used a mandatory standard or technical regulation for iodized salt under their Food Act/Law. The remainder have developed a 'stand-alone' Law/Act. Available national surveys indicate that the proportion of households consuming adequately iodized salt was lowest in countries with no, draft or voluntary legislation, and highest in those where the legislation was based on mandatory regulations under Food Acts/Laws. CONCLUSIONS: Legislation for salt iodization, particularly mandatory legislation under the national food law, facilitates universal salt iodization. However, additional important factors for implementation of salt iodization and maintenance of achievements include the salt industry's structure and capacity to adequately fortify, and official commitment and capacity to enforce national legislation.


Subject(s)
Deficiency Diseases/prevention & control , Food, Fortified , Health Plan Implementation , Iodine/deficiency , Legislation, Food , Sodium Chloride, Dietary/therapeutic use , Asia/epidemiology , Deficiency Diseases/epidemiology , Food, Fortified/standards , Health Plan Implementation/legislation & jurisprudence , Health Plan Implementation/trends , Humans , Iodine/standards , Iodine/therapeutic use , Legislation, Food/trends , Mandatory Programs/legislation & jurisprudence , Pacific Islands/epidemiology , Risk , Sodium Chloride, Dietary/standards , Voluntary Programs/legislation & jurisprudence
5.
Fed Regist ; 79(174): 53519-70, 2014 Sep 09.
Article in English | MEDLINE | ID: mdl-25233531

ABSTRACT

This rule governs the secure disposal of controlled substances by registrants and ultimate users. These regulations will implement the Secure and Responsible Drug Disposal Act of 2010 by expanding the options available to collect controlled substances from ultimate users for the purpose of disposal, including: Take-back events, mail-back programs, and collection receptacle locations. These regulations contain specific language allowing law enforcement to voluntarily continue to conduct take-back events, administer mail-back programs, and maintain collection receptacles. These regulations will allow authorized manufacturers, distributors, reverse distributors, narcotic treatment programs (NTPs), hospitals/clinics with an on-site pharmacy, and retail pharmacies to voluntarily administer mail-back programs and maintain collection receptacles. In addition, this rule expands the authority of authorized hospitals/clinics and retail pharmacies to voluntarily maintain collection receptacles at long-term care facilities. This rule also reorganizes and consolidates previously existing regulations on disposal, including the role of reverse distributors.


Subject(s)
Drug and Narcotic Control/legislation & jurisprudence , Legislation, Drug , Prescription Drug Diversion/legislation & jurisprudence , Refuse Disposal/legislation & jurisprudence , Humans , Prescription Drug Diversion/prevention & control , United States , Voluntary Programs/legislation & jurisprudence
6.
Z Evid Fortbild Qual Gesundhwes ; 107(4-5): 327-34, 2013.
Article in German | MEDLINE | ID: mdl-23916273

ABSTRACT

After 1945 the common medical training infrastructure was broken up into two different political systems. While in the Federal Republic of Germany the structure was based on physicians' self-governance, in the German Democratic Republic medical professional structures were organised by the government. After the unification of the two German states, which took place on October 3, 1990, the centralistic structure was replaced by the system of physician self-governance. Before January 1, 2004, continuing medical education (CME) in West Germany relied on a system of voluntary obligations. In East Germany, though, professional CMEs were compulsory; they were called "obligatorische periphere Fortbildung." Based on 15 expert interviews on the topic of "CME in Germany", the different circumstances and conditions were analysed taking account of the historical background. Only selected professionals with experience in both German states (one with a federal, the other with a centralistic system), were chosen for the survey.


Subject(s)
Contract Services/history , Contract Services/legislation & jurisprudence , Education, Medical, Continuing/history , Education, Medical, Continuing/legislation & jurisprudence , Mandatory Programs/history , Mandatory Programs/legislation & jurisprudence , National Health Programs/history , National Health Programs/legislation & jurisprudence , Social Change/history , Voluntary Programs/history , Voluntary Programs/legislation & jurisprudence , Clinical Competence/legislation & jurisprudence , Curriculum , Germany, East , Germany, West , History, 19th Century , History, 20th Century , History, 21st Century , Humans , Politics
7.
Fed Regist ; 78(150): 47154-79, 2013 Aug 05.
Article in English | MEDLINE | ID: mdl-23923139

ABSTRACT

The Food and Drug Administration (FDA or we) is issuing a final rule to define the term "gluten-free'' for voluntary use in the labeling of foods. The final rule defines the term "gluten-free'' to mean that the food bearing the claim does not contain an ingredient that is a gluten-containing grain (e.g., spelt wheat); an ingredient that is derived from a gluten-containing grain and that has not been processed to remove gluten (e.g., wheat flour); or an ingredient that is derived from a gluten-containing grain and that has been processed to remove gluten (e.g., wheat starch), if the use of that ingredient results in the presence of 20 parts per million (ppm) or more gluten in the food (i.e., 20 milligrams (mg) or more gluten per kilogram (kg) of food); or inherently does not contain gluten; and that any unavoidable presence of gluten in the food is below 20 ppm gluten (i.e., below 20 mg gluten per kg of food). A food that bears the claim "no gluten,'' "free of gluten,'' or "without gluten'' in its labeling and fails to meet the requirements for a "gluten-free'' claim will be deemed to be misbranded. In addition, a food whose labeling includes the term "wheat'' in the ingredient list or in a separate "Contains wheat'' statement as required by a section of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) and also bears the claim "gluten-free'' will be deemed to be misbranded unless its labeling also bears additional language clarifying that the wheat has been processed to allow the food to meet FDA requirements for a "gluten-free'' claim. Establishing a definition of the term "gluten-free'' and uniform conditions for its use in food labeling will help ensure that individuals with celiac disease are not misled and are provided with truthful and accurate information with respect to foods so labeled. We are issuing the final rule under the Food Allergen Labeling and Consumer Protection Act of 2004 (FALCPA).


Subject(s)
Diet, Gluten-Free/classification , Food Labeling/legislation & jurisprudence , Celiac Disease/complications , Celiac Disease/diet therapy , Celiac Disease/etiology , Diet, Gluten-Free/standards , Food Labeling/standards , Glutens/adverse effects , Humans , United States , Voluntary Programs/legislation & jurisprudence
9.
Bull World Health Organ ; 91(2): 142-5, 2013 Feb 01.
Article in English | MEDLINE | ID: mdl-23554527

ABSTRACT

Twelve agencies of the United Nations, including the World Health Organization, have issued a joint statement that calls on Member States to replace the compulsory detention of people who use opioids in treatment centres with voluntary, evidence-informed and rights-based health and social services. The arguments in favour of this position fall into three broad categories: Compulsory treatment centres infringe on an individual's liberty, they put human beings at risk of harm, and evidence of their effectiveness against opioid dependence has not been generated. The United Nations statement underscores that although countries apply different criteria for sending individuals to compulsory treatment centres, detention often takes place without due process, legal safeguards or judicial review. This clearly violates internationally recognized human rights standards. Furthermore, people who are committed to these centres are often exposed to physical and sexual violence, forced labour and sub-standard living conditions. They are often denied health care, despite their heightened vulnerability to HIV infection and tuberculosis. Finally, there is no evidence, according to the statement, that these centres offer an environment that is conducive to recovery from opioid dependence or to the rehabilitation of commercial sex workers or of children who have suffered sexual exploitation, abuse or lack of care and protection. The author of this paper sets forth several arguments that counter the position taken by the United Nations and argues in favour of compulsory treatment within a broader harm reduction strategy aimed at protecting society as well as the individual concerned.


Douze agences des Nations Unies, parmi elles l'Organisation mondiale de la Santé, ont émis une déclaration commune qui appelle les États membres à remplacer la détention obligatoire des consommateurs d'opioïdes dans des centres de traitement par des services sanitaires et sociaux volontaires qui s'appuient sur des données probantes et soient fondés sur le droit. Les arguments en faveur de cette position se répartissent en trois grandes catégories: les centres de traitement obligatoire empiètent sur la liberté de l'individu, ils exposent les êtres humains à des risques et la preuve de leur efficacité contre la dépendance aux opioïdes n'a pas été démontrée. La déclaration des Nations Unies souligne que même si les pays appliquent des critères différents pour l'envoi des individus dans des centres de traitement obligatoire, leur détention survient souvent sans procédure régulière, protection légale ou contrôle juridictionnel. Cet état de fait contrevient clairement aux normes des droits de l'homme reconnues au niveau international. En outre, les personnes remises à ces centres sont souvent exposées à des sévices physiques et sexuels, à du travail forcé et à des conditions de vie inférieures aux normes. Ils se voient souvent refuser des soins de santé en dépit de leur vulnérabilité accrue à l'infection par le VIH et à la tuberculose. Enfin, il n'y a aucune preuve, selon cette déclaration, que ces centres offrent un climat propice à la récupération de la dépendance aux opioïdes ou à la réinsertion des professionnels du sexe ou des enfants victimes d'exploitation sexuelle, de maltraitance ou de manque de soins et de protection.L'auteur de ce document de travail avance plusieurs arguments contraires à la position adoptée par les Nations Unies et milite en faveur d'un traitement obligatoire participant d'une stratégie élargie de réduction des risques visant à protéger la société, mais aussi l'individu concerné.


Doce agencias de las Naciones Unidas, entre ellas la Organización Mundial de la Salud, han emitido una declaración conjunta que insta a los Estados miembros a reemplazar la retención obligatoria en centros de tratamiento de personas que hacen uso de opiáceos por servicios sociales y sanitarios voluntarios, basados en pruebas científicas y en sus derechos. Los argumentos a favor de esta postura se clasifican en tres amplias categorías: Los centros de tratamiento obligatorio atentan contra la libertad individual, ponen a las personas en riesgo y no existen pruebas de su eficacia contra la dependencia de opiáceos. La declaración de las Naciones Unidas enfatiza que, aunque cada país aplica criterios distintos a la hora de enviar a los individuos a los centros de tratamiento obligatorio, es frecuente que la retención se lleve a cabo sin el debido proceso, la seguridad jurídica ni el examen judicial correspondiente, lo que viola claramente las normas de los derechos humanos reconocidas a nivel internacional. Además, las personas internadas en dichos centros se ven expuestas, con frecuencia, a violencia física o sexual, trabajos forzados y condiciones precarias de vida, y es frecuente que se les niegue la atención sanitaria a pesar de ser más vulnerables a la infección por VIH y a la tuberculosis. Por último, no hay ninguna evidencia, de acuerdo con la declaración, de que dichos centros ofrezcan un ambiente propicio para la recuperación de la dependencia a los opiáceos o para la rehabilitación de trabajadores sexuales o de niños que han sufrido explotación sexual, abusos o falta de cuidado y atención.El autor del presente artículo describe numerosos argumentos que rebaten la posición adoptada por las Naciones Unidas a favor de un tratamiento obligatorio en el ámbito de una estrategia más amplia enfocada a la reducción del daño y cuyo objetivo es proteger tanto a la sociedad como al individuo afectado.


Subject(s)
HIV Infections/prevention & control , Health Services Accessibility/legislation & jurisprudence , Human Rights/legislation & jurisprudence , Opioid-Related Disorders/rehabilitation , Substance Abuse Treatment Centers/legislation & jurisprudence , Tuberculosis/prevention & control , Dissent and Disputes , Evidence-Based Practice/legislation & jurisprudence , Evidence-Based Practice/standards , Global Health/legislation & jurisprudence , HIV Infections/transmission , Harm Reduction/ethics , Health Services Accessibility/standards , Health Services Accessibility/trends , Humans , Mandatory Programs/ethics , Mandatory Programs/legislation & jurisprudence , Opioid-Related Disorders/complications , Risk Assessment , Social Problems/ethics , Social Problems/legislation & jurisprudence , Social Problems/prevention & control , Substance Abuse Treatment Centers/ethics , Substance Abuse Treatment Centers/organization & administration , Treatment Refusal/ethics , Treatment Refusal/legislation & jurisprudence , Tuberculosis/transmission , United Nations/legislation & jurisprudence , United Nations/standards , Voluntary Programs/ethics , Voluntary Programs/legislation & jurisprudence
11.
Can J Public Health ; 102(6): 414-6, 2011.
Article in English | MEDLINE | ID: mdl-22164548

ABSTRACT

The discontinuation of the Canadian long-form mandatory census presents a crisis for data users. Examined as a tension between the need to preserve individual civil liberties and the need to curtail those liberties for the public good, the census crisis presents an opportunity for a public discussion on the specifics of our national values, beliefs and expectations.


Subject(s)
Censuses , Civil Rights/legislation & jurisprudence , Personal Autonomy , Public Health/legislation & jurisprudence , Public Policy , Attitude of Health Personnel , Biomedical Research/ethics , Canada , Civil Rights/standards , Data Collection/ethics , Data Collection/legislation & jurisprudence , Humans , Informed Consent/legislation & jurisprudence , Mandatory Programs/legislation & jurisprudence , Mandatory Programs/trends , Politics , Public Health/standards , Voluntary Programs/legislation & jurisprudence , Voluntary Programs/trends
12.
Daedalus ; 140(4): 140-53, 2011.
Article in English | MEDLINE | ID: mdl-22167915

ABSTRACT

Volunteers and charitable organizations contribute significantly to community welfare through their prosocial behavior: that is, discretionary behavior such as assisting, comforting, sharing, and cooperating intended to help worthy beneficiaries. This essay focuses on prosocial behavior on the Internet. It describes how offline charitable organizations are using the Net to become more efficient and effective. It also considers entirely new models of Net-based volunteer behavior directed at creating socially beneficial information goods and services. After exploring the scope and diversity of online prosocial behavior, the essay focuses on ways to encourage this kind of behavior through appropriate task and social structures, motivational signals, and trust indicators. It concludes by asking how local offline communities ultimately could be diminished or strengthened as prosocial behavior increases online.


Subject(s)
Charities , Fund Raising , Internet , Social Behavior , Social Welfare , Voluntary Programs , Charities/economics , Charities/education , Charities/history , Charities/legislation & jurisprudence , Cultural Diversity , Fund Raising/economics , Fund Raising/history , Fund Raising/legislation & jurisprudence , History, 20th Century , History, 21st Century , Information Services/economics , Information Services/history , Information Services/legislation & jurisprudence , Internet/economics , Internet/history , Social Behavior/history , Social Welfare/economics , Social Welfare/ethnology , Social Welfare/history , Social Welfare/legislation & jurisprudence , Social Welfare/psychology , Voluntary Programs/economics , Voluntary Programs/history , Voluntary Programs/legislation & jurisprudence , Volunteers/education , Volunteers/history , Volunteers/legislation & jurisprudence , Volunteers/psychology
13.
Econ Dev Cult Change ; 59(2): 387-416, 2011.
Article in English | MEDLINE | ID: mdl-21174884

ABSTRACT

This article investigates the targeting of cyclone relief within villages in Fiji. It focuses on how relief allocation is linked with informal risk sharing and elite capture, both of which are directly related to kinship. The results are as follows. First, food aid is initially targeted toward kin groups according to their aggregate shocks and then shared among group members. Right after the cyclone, when aid is scarce, households with damage to their housing and with greater crop damage are allocated less aid within the group. Instead, they receive greater net private transfers in other forms, especially in labor sharing. Consistent patterns are found in village, cropping, and housing rehabilitations. Second, there is no elite capture of food aid in the kin group, and instead, traditional kin leaders share food with others; however, non-kin-based community leaders capture aid when it is allocated across kin groups. Third, distinct from food aid demanded by all, tarpaulins demanded by victims only strongly target individual housing damage at the village level­not the kin group­independent of social status. As with food aid, victims with greater crop damage are given a lower priority. Implications for relief policies are discussed.


Subject(s)
Agriculture , Community Networks , Cyclonic Storms , Food Supply , Relief Work , Volunteers , Agriculture/economics , Agriculture/education , Agriculture/history , Community Networks/economics , Community Networks/history , Cyclonic Storms/history , Disaster Planning/economics , Disaster Planning/history , Fiji/ethnology , Food Supply/economics , Food Supply/history , History, 20th Century , History, 21st Century , Public Health/economics , Public Health/education , Public Health/history , Relief Work/economics , Relief Work/history , Social Conditions/economics , Social Conditions/history , Social Conditions/legislation & jurisprudence , Voluntary Programs/economics , Voluntary Programs/history , Voluntary Programs/legislation & jurisprudence , Volunteers/education , Volunteers/history , Volunteers/legislation & jurisprudence , Volunteers/psychology
14.
Soc Sci Q ; 91(5): 1369-89, 2010.
Article in English | MEDLINE | ID: mdl-21125763

ABSTRACT

Objective. Disasters are a regular occurrence throughout the world. Whether all eligible victims of a catastrophe receive similar amounts of aid from governments and donors following a crisis remains an open question.Methods. I use data on 62 similarly damaged inland fishing villages in five districts of southeastern India following the 2004 Indian Ocean tsunami to measure the causal influence of caste, location, wealth, and bridging social capital on the receipt of aid. Using two-limit tobit and negative binomial models, I investigate the factors that influence the time spent in refugee camps, receipt of an initial aid packet, and receipt of 4,000 rupees.Results. Caste, family status, and wealth proved to be powerful predictors of beneficiaries and nonbeneficiaries during the aid process.Conclusion. While many scholars and practitioners envision aid distribution as primarily a technocratic process, this research shows that discrimination and financial resources strongly affect the flow of disaster aid.


Subject(s)
International Cooperation , Public Assistance , Social Class , Social Responsibility , Socioeconomic Factors , Tsunamis , Disasters/economics , Disasters/history , History, 21st Century , Humans , India/ethnology , International Cooperation/history , International Cooperation/legislation & jurisprudence , Population Groups/education , Population Groups/ethnology , Population Groups/history , Population Groups/legislation & jurisprudence , Population Groups/psychology , Prejudice , Public Assistance/economics , Public Assistance/history , Public Assistance/legislation & jurisprudence , Social Class/history , Socioeconomic Factors/history , Tsunamis/economics , Tsunamis/history , Voluntary Programs/economics , Voluntary Programs/history , Voluntary Programs/legislation & jurisprudence
15.
Fed Regist ; 75(235): 76256-9, 2010 Dec 08.
Article in English | MEDLINE | ID: mdl-21140595

ABSTRACT

We are modifying our regulations to establish a 12-month time limit for the withdrawal of old-age benefits applications, allow one withdrawal per lifetime, and limit the voluntary suspension of benefits for purposes of receiving delayed retirement credits to months for which you have not received a payment. We are making these changes to revise current policies that have the potential for misuse.


Subject(s)
Retirement/legislation & jurisprudence , Social Security/legislation & jurisprudence , Employment , Humans , Income , Retirement/economics , Social Security/economics , Time Factors , United States , Voluntary Programs/economics , Voluntary Programs/legislation & jurisprudence
16.
Popul Dev Rev ; 36(3): 487-510, 2010.
Article in English | MEDLINE | ID: mdl-20882703

ABSTRACT

Having reversed its pronatalist policies in 1988, the Islamic Republic of Iran implemented one of the most successful family planning programs in the developing world. This achievement, particularly in urban centers, is largely attributable to a large women-led volunteer health worker program for low-income urban neighborhoods. Research in three cities demonstrates that this successful program has had a host of unintended consequences. In a context where citizen mobilization and activism are highly restricted, volunteers have seized this new state-sanctioned space and successfully negotiated many of the familial, cultural, and state restrictions on women. They have expanded their mandate from one focused on health activism into one of social, if not political, activism, highlighting the ways in which citizens blur the boundaries of state and civil society under restrictive political systems prevalent in many of the Middle Eastern societies.


Subject(s)
Family Planning Policy , Public Health , Social Control Policies , Volunteers , Women, Working , Developing Countries/economics , Developing Countries/history , Family Planning Policy/economics , Family Planning Policy/history , Family Planning Policy/legislation & jurisprudence , Government Programs/economics , Government Programs/education , Government Programs/history , Government Programs/legislation & jurisprudence , History, 20th Century , History, 21st Century , Iran/ethnology , Public Health/economics , Public Health/education , Public Health/history , Public Health/legislation & jurisprudence , Social Change/history , Social Control Policies/economics , Social Control Policies/history , Social Control Policies/legislation & jurisprudence , Socioeconomic Factors/history , Urban Population/history , Voluntary Programs/economics , Voluntary Programs/history , Voluntary Programs/legislation & jurisprudence , Volunteers/education , Volunteers/history , Volunteers/legislation & jurisprudence , Volunteers/psychology , Women's Health/ethnology , Women's Health/history , Women's Rights/economics , Women's Rights/education , Women's Rights/history , Women's Rights/legislation & jurisprudence , Women, Working/education , Women, Working/history , Women, Working/legislation & jurisprudence , Women, Working/psychology
18.
Sociol Inq ; 80(3): 448-74, 2010.
Article in English | MEDLINE | ID: mdl-20827857

ABSTRACT

The study of civic activity has become a central focus for many social scientists over the past decade, generating considerable research and debate. Previous studies have largely overlooked the role of youth socialization into civic life, most notably in the settings of home and school. Further, differences along gender lines in civic capacity have not been given sufficient attention in past studies. This study adds to the literature by examining the potential pathways in the development of youth civic activity and potential, utilizing both gender-neutral and gender-specific structural equation modeling of data from the 1996 National Household Education Survey. Results indicate that involvement by parents in their child's schooling plays a crucial, mediating role in the relationship between adult and youth civic activity. Gender differences are minimal; thus adult school involvement is crucial for transmitting civic culture from parents to both female and male youth.


Subject(s)
Gender Identity , Psychology, Adolescent , Social Identification , Social Sciences , Socialization , Voluntary Programs , Adolescent , Adolescent Behavior/ethnology , Adolescent Behavior/physiology , Adolescent Behavior/psychology , History, 20th Century , History, 21st Century , Humans , Parent-Child Relations/ethnology , Parent-Child Relations/legislation & jurisprudence , Psychology, Adolescent/education , Psychology, Adolescent/history , Social Change/history , Social Conditions/economics , Social Conditions/history , Social Conditions/legislation & jurisprudence , Social Sciences/education , Social Sciences/history , United States/ethnology , Voluntary Programs/economics , Voluntary Programs/history , Voluntary Programs/legislation & jurisprudence , Volunteers/education , Volunteers/history , Volunteers/legislation & jurisprudence , Volunteers/psychology
19.
Fed Regist ; 75(152): 47712-3, 2010 Aug 09.
Article in English | MEDLINE | ID: mdl-20695128

ABSTRACT

This final rule eliminates the 1 year lock out for non-Active Duty members who disenroll from TRICARE Prime before their annual enrollment renewal date.


Subject(s)
Eligibility Determination/legislation & jurisprudence , Health Benefit Plans, Employee/legislation & jurisprudence , Humans , Military Personnel/legislation & jurisprudence , United States , Voluntary Programs/legislation & jurisprudence
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