scholarly journals The Halls Creek Community Families Program: Elements of the role of the child health nurse in development of a remote Aboriginal home visiting peer support program for families in the early years

2015 ◽  
Vol 23 (6) ◽  
pp. 322-326 ◽  
Author(s):  
Ailsa Munns ◽  
Roz Walker
Author(s):  
Dezarie Moskal ◽  
Holly Whitaker ◽  
Julia F. Bernstein ◽  
Stephen A. Maisto ◽  
Gerard J. Connors

Author(s):  
Jason Dawson ◽  
Mary Johnston ◽  
Nancy Kehiayan ◽  
Susan Kyanko ◽  
Ruby Martinez

2013 ◽  
Vol 2013 ◽  
pp. 1-7 ◽  
Author(s):  
Louisa Ng ◽  
Bhasker Amatya ◽  
Fary Khan

Background/Objectives. This pilot study evaluated the impact of a peer support program on improving multiple sclerosis (MS) related psychological functions (depression, anxiety, and stress) and enhancing quality of life. Methodology. Participants (n=33) were recruited prospectively and received an 8-week group face-to-face peer support program. Assessments were at baseline (T1), 6 weeks after program (T2), and 12 months after program (T3), using validated questionnaires: Depression Anxiety Stress Scale (DASS), McGill Quality of Life (MQOL), and Brief COPE. Results. Participants’ mean age was 52; the majority were female (64%) and married (64%). Median time since MS diagnosis was 16 years. At T2, participants reported improved psychological functioning (DASS “depression,” “anxiety,” and “stress” subscales, z values −2.36, −2.22, and −2.54, moderate effect sizes (r) 0.29, 0.28, and 0.32, resp.) and quality of life (MQOL SIS z score −2.07, r=0.26) and were less likely to use “self-blame” as a coping mechanism (Brief COPE z score −2.37, r=0.29). At T3, the positive improvements in stress (DASS stress subscale z score −2.41, r=0.31) and quality of life were maintained (MQOL SIS, z score −2.30, r=0.29). There were no adverse effects reported.


2014 ◽  
Vol 65 (9) ◽  
pp. 1177-1177 ◽  
Author(s):  
Shaili Jain ◽  
Julia M. Hernandez ◽  
Steven E. Lindley

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