{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,29]],"date-time":"2026-08-29T01:49:14Z","timestamp":1787968154795,"version":"build-2784847793"},"reference-count":79,"publisher":"Wiley","issue":"10","license":[{"start":{"date-parts":[[2013,5,9]],"date-time":"2013-05-09T00:00:00Z","timestamp":1368057600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Psycho-Oncology"],"published-print":{"date-parts":[[2013,10]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>Objective<\/jats:title>\n                    <jats:p>Although chemotherapy\u2010induced cognitive impairment is common among breast cancer patients, evidence for effective interventions addressing cognitive deficits is limited. This randomized controlled trial examined the feasibility and preliminary efficacy of a Tibetan Sound Meditation (TSM) program to improve cognitive function and quality of life in breast cancer patients.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>Forty\u2010seven breast cancer patients (mean age 56.3\u2009years), who were staged I\u2013III at diagnosis, 6\u201360\u2009months post\u2010chemotherapy, and reported cognitive impairment at study entry were recruited. Participants were randomized to either two weekly TSM sessions for 6\u2009weeks or a wait list control group. Neuropsychological assessments were completed at baseline and 1\u2009month post\u2010treatment. Self\u2010report measures of cognitive function (Functional Assessment of Cancer Therapy (FACT)\u2010Cog), quality of life (SF\u201036), depressive symptoms (Center for Epidemiologic Studies Depression Scale), sleep disturbance (Pittsburgh Sleep Quality Index), fatigue (Brief Fatigue Inventory), and spirituality (FACT\u2010Sp) were completed at baseline, the end of treatment, and 1\u2009month later.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      Relative to the control group, women in the TSM group performed better on the verbal memory test (Rey Auditory Verbal Learning Test trial 1) (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.06) and the short\u2010term memory and processing speed task (Digit Symbol) (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.09) and reported improved cognitive function (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.06), cognitive abilities (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.08), mental health (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.04), and spirituality (\n                      <jats:italic>p<\/jats:italic>\n                      \u2009=\u20090.05) at the end of treatment but not 1\u2009month later.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>This randomized controlled trial revealed that TSM program appears to be a feasible and acceptable intervention and may be associated with short\u2010term improvements in objective and subjective cognitive function as well as mental health and spirituality in breast cancer patients. Copyright \u00a9 2013 John Wiley &amp; Sons, Ltd.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1002\/pon.3296","type":"journal-article","created":{"date-parts":[[2013,5,9]],"date-time":"2013-05-09T04:00:58Z","timestamp":1368072058000},"page":"2354-2363","source":"Crossref","is-referenced-by-count":97,"title":["Tibetan sound meditation for cognitive dysfunction: results of a randomized controlled pilot trial"],"prefix":"10.1002","volume":"22","author":[{"given":"K.","family":"Milbury","sequence":"first","affiliation":[{"name":"Department of General Oncology The University of Texas MD Anderson Cancer Center  Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A.","family":"Chaoul","sequence":"additional","affiliation":[{"name":"Department of General Oncology The University of Texas MD Anderson Cancer Center  Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"K.","family":"Biegler","sequence":"additional","affiliation":[{"name":"Health Policy Research Institute, University of California  Irvine CA USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T.","family":"Wangyal","sequence":"additional","affiliation":[{"name":"Ligmincha Institute  Shipman VA USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"A.","family":"Spelman","sequence":"additional","affiliation":[{"name":"Department of General Oncology The University of Texas MD Anderson Cancer Center  Houston Texas USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C. 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