There is not much research on specifically MBSR in BC survivors, but there is enough to show a promising future for patients who continue with MBSR practice. These studies had some limitations which were consistent throughout some and different for others. These limitations are important to know so the next study can be mindful of excluding that limitation. A common problem with MBSR studies was that few participants continued practicing a formal form of MBSR after program completion. Carmody and Baer explicated noted that time spent engaging in a formal practice lead to more improvements in areas of mindfulness and measures of symptoms and well-being. It is also said the most stress state a women with breast cancer will be in is 1 year after …show more content…
Lengacher’s 2010 study had a problem of non-attendance but the reason behind it was follow up appointments that could not be changed. Also the findings of this study are directly applicable to a specific population of Stage 0 and Stage 1 BC patients who were treated with primarily radiation (no chemotherapy). Both Legacher’s 2010 study and Matousek’s study had a small sample size, no control group or a follow up evaluation for participants, these limitations could easily be avoided in a future study. The participants were mostly Caucasian. It would be beneficial for studies to have a more diverse pool of participants. There is a cultural health gap between many ethnic groups in the United States. To bridge this gap and provide equal interventions to everyone it is important to teach about what MBSR is to cancer patients of all ethnicities. Future research should look at the population of BC patients who are recently diagnosed as …show more content…
Their population was patients from stage 0-3 who had completed treatment. Data was self reported on measures of psychological, physical symptoms and quality of life. The program was home based and the design was to deliver 2-hour weekly sessions for 6 weeks on an iPad. There mean age of the 15 participants was 58, one participants was Black Non-Hispanic and the remaining were White Non-Hispanic. There were 13 who completed the study and they showed significant improvement from pre-MBSR to post-MBSR in symptoms of depression, anxiety, stress, fear ofrecurrence, sleep quality, fatigue and quality of life (Lengacher, Ramesar, Reich, Paterson, Moscoso, & Carranza, 2014). This study really supported the idea that is a home based program is a great option and the clinical impact really supported the idea. It allowed the participants flexibility and they could also practice in their own judgment free zone which is really important in
Per Pauline and Terence, you overlooked quite a few things such as (1) 2 chemo patients with the incorrect treatment dates, (2) hamp1/hamp2
According to the data, the intervention phase was successful because my target was reduced to feeling stressed less than three times a day. The baseline mean of frequency of
Having cancer frequently forces patients into changing their lifestyles for the better. It is proven that making positive lifestyle changes decreases the chances that cancer will recur. "Many patients and survivors worry about cancer coming back after treatment. Evidence suggests that making positive lifestyle changes during and after cancer treatment may help prevent a recurrence or second cancer" (Healthy Living After Cancer). This can show how the fear of the recurrence of cancer can drive the former cancer patient into being healthier.
Between the time span of the study of diverse patients, the naturalistic study sees how well the patients function in society. It involves observing participants in their natural environment. This kind of research is often used in situations, conducting laboratory research because it is cost prohibitive, impractical, or would immensely impact the participant's behavior. The reason why this research is necessary is because there has not been a lot of research on what treatment is most effective for this disorder. Therapists and patients in a community were recruited for the existing
When reading each case study, I became intrigued by the approach done for Brandon’s case study. I think the approach that was used for Brandon would be effective in my own practice, because the approach helps the clinician to understand the
The study proves a need for improvement in our health delivery systems around cultural competency. If healthcare providers understand cultural perspectives around illnesses, providers will understand what shapes African American health experiences and decision-making (Omenka et al., 2020). For example, African Americans view diseases such as cancer as a spiritual issue, so they are more likely to seek traditional healing in their home countries (Omenka et al., 2020). The African American individuals will not want the typical treatment of chemotherapy that is used in the United States to treat cancer. With a lack of culturally competent providers in the United States, African Americans are more likely to have a distrust in health systems, which can put them at risk of negative health outcomes.
Furthermore, it was very beneficial for the researchers to evaluate the LHSV as the method to gather the required information. The survey consisted of twelve questions that were descriptive and direct; which, offered “Yes” or “No” answers and multiple choice questions (option of three responses). I feel the design of the survey was carefully created to help the veterans fully understand the questions and answer them to the best of their ability. Although I admired these dynamics in the study, the external validity I feel was below average. Since this was one of the first studies to compare health behaviors with mental illness among the veterans, the study is based on one type of population; which, results do not represent the entire community of individuals that have BPD.
They also share commonalities in having the best research and clinical skills using scientific-based research to convey assessments and interventions. In order for clients to receive the best treatment we must use empirical science and evaluate treatment data to evaluate and make sure clients are receiving the best treatment possible for their individual needs. Furthermore, scientific approaches can ensure us that the interventions utilize should be the most effective. It is important that scientific practice provides us with the ability to acquire skills to evaluate and formulate hypothesis. The scientific-practitioner model ties into the BCBA guidelines as well.
The sample consisted of 85 patients with selected cancers undergoing radiation therapy. The investigator collected the socio demographic and clinical data from patients who fulfilled the inclusion criteria. The descriptive analysis of the socio demographic variables revealed
As cancer continued to become more prevalent, health care providers and researchers were forced to further investigate the biology, development, and treatment of cancer. The interaction of cancer outside the realm of molecular and cellular biology became apparent in the mid 1900’s and has since found importance in the fields of psychology, neuropsychology, and psychosocial oncology (Holland, 2002). The field of psychosocial oncology finally became established in the 1970’s, when the stigma of cancer shifted, and patients felt comfortable sharing their experience (Holland, 2002). Social workers and nurses were the first health care professionals to attend to the psychological needs of
Treatment Evaluation Treatment evaluation is an evidence-based that a practitioner incorporates with well-researched interventions providing clinical experience and ethics, as well as, culture to conduct also, to inspire the delivery treatments and services. However, evaluation informs a client whether a service given was appropriate or not. Moreover, at the micro level practice, evaluation helps practitioners to know how successful their work with a client has been and how satisfied client were with the services provided. On the other hand, at the mezzo level, practitioners want to know whether the treatment achieved its purposes. Also, to see if, the group members achieved their set goals.
Though the hypothesis of this study was accepted, certain limitations were present. The intervention time, if longer, could have included more
The Crisis of Cancer: A Quasi-Qualitative Study of Program Assessment Based on Intervention Programs Dealing With Cancer Patients Michelle Nikka R. Carabeo Keziah Liezl D. Dolojan PSYB-3 Abstract A cancer diagnosis can greatly affect the patient as well as the family members. This quasi qualitative study aims to study the impact of cancer on the psychological well-being of cancer patients and their families.
The authors reported that there were some things that limited the success of this study. One of these things was that they only focused on one patient, this meant that the results gathered cannot be generalized. Another thing that limited the
(Ogden. 2017). Individual health beliefs and behavior thus plays a big role on the initiation, detection and treatment phase. This factor influences the experience one have with cancer, when and how they seek medical help, and the way they deal with the pain and changes that ensues. Experiencing chronic illness leads to a lot of physical symptoms in the person which has in turn has a negative effect on the person's behaviour. Stress factor: "Stress has also been shown to have a role in cancer particularly if the stressor."