Effect of Music Therapy on Pain and Quality of Life among Cancer Survivors

Abstract Background: Cancer is one of the ten leading cause of death in India. Cancer patients usually present with moderate to severe pain which results usually from the cancer itself or from their treatment .To counteract pain complementary therapies are used along with the medical treatment. The most common used in the clinical setting is Music therapy; which is found to have a positive effect on the physical and psychological response of the patients. Objectives: To find the effectiveness of Music therapy on Pain and Quality of life among Cancer survivors. Material and Method : A quasi experimental research design was adopted for the study. The data were collected using demographic proforma, Numerical Pain rating scale and McGill Quality of life Questionnaire. 50 subjects with moderate to severe pain were identified and were randomly allocated into experimental (25) and control group (25). Experimental groups (25) received Music therapy for 15-20 mins twice a day for a period of 5 days. The control group (25) received no intervention. Pain was assessed twice a day, before and after the intervention for 5 th th days and QoL was assessed on the 6th and 10th day for both the groups.. Results: Majority of the subjects19 (38%) were between the age groups of 41-50 years and most of them 29 (58%) were males. Among the females the most common cancer was breast 12 (24%) and among males it was lungs 10 (20%). Most of the subjects 23(46%) had stage –II cancer, and 28(56%) were on radiation therapy. With regard to treatment, majority 29(58%) were on treatment for a duration of 1-3 months. The study also revealed a significant difference in the level of pain after the music intervention (p<0.05) and a significant improvement in the Quality of life especially affecting the physical and psychological domain (p<0.05). No significant association was found between pain, QoL and selected demographic variables (p<0.05) Conclusion: Music therapy was found to be an effective complementary therapy in reducing the level of pain and improving the QoL of the cancer survivors.

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Efficacy and safety of electro-acupuncture (EA) on insomnia in patients with lung cancer: study protocol of a randomized controlled trial

Trials ◽

10.1186/s13063-020-04721-4 ◽

2020 ◽

Vol 21 (1) ◽

Author(s):

Hongyu Yue ◽

Shuang Zhou ◽

Huangan Wu ◽

Xuan Yin ◽

Shanshan Li ◽

...

Keyword(s):

Quality Of Life ◽

Lung Cancer ◽

Cancer Survivors ◽

Controlled Trial ◽

Control Group ◽

Life Questionnaire ◽

Efficacy And Safety ◽

Symptom Scale ◽

Significance Level

Abstract Background Cancer-related insomnia (CRI) is one of the most prevalent complaints among cancer survivors and severely impairs patients’ quality of life. As a popular non-pharmacological alternative treatment, acupuncture provides a good clinical curative effect on insomnia. The aim of this trial is to evaluate efficacy and safety of electro-acupuncture on insomnia in patients with lung cancer. Method This is a protocol for a multicenter randomized single-blinded sham-controlled trial. We will randomly assign 252 eligible patients with lung cancer-related insomnia into two groups at a ratio of 1:1, the treatment group (EA) and the control group (sham EA). All treatment will be given 3 times per week for 8 weeks, and a 12-week follow-up will be conducted. The primary outcome will be measured by the Pittsburgh Sleep Quality Index (PSQI). The secondary outcomes will include sleep parameters recorded from the actigraphy, scores from Quality of Life Questionnaire Core-30 (QLQ-C30), and Patient Health Questionnaire-9 (PHQ-9). All adverse effects during the trial will be assessed by the Treatment Emergent Symptom Scale (TESS). All analyses will be based on ITT principle and performed with the statistical software SPSS (version 24.0) by t test, rank-sum test, chi-square, and so on. A two-sided significance level will be set at 5%. Discussion This large-sample trial protocol will evaluate the efficacy of electro-acupuncture on insomnia in patients with lung cancer. This protocol, if proven to be effective, will contribute to filling the gap in treatment options in the CRI field and provide a promising intervention for insomnia in lung cancer survivors. Trial registration ChiCTR ChiCTR1900026395. Registered on 8 October 2019, http://www.chictr.org.cn/showproj.aspx?proj=44068

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Comparison of the effect of Myrtus communis herbal and anti-hemorrhoid ointments on the hemorrhoid symptoms and quality of life in postpartum women with grade I and II internal hemorrhoid: A triple-blinded randomized controlled clinical trial

Journal of Complementary and Integrative Medicine ◽

10.1515/jcim-2018-0147 ◽

2019 ◽

Vol 16 (4) ◽

Cited By ~ 1

Author(s):

Jamileh Malekuti ◽

Mojgan Mirghafourvand ◽

Khadijeh Samadi ◽

Fatemeh Abbasalizadeh ◽

Laleh Khodaei

Keyword(s):

Quality Of Life ◽

Intervention Group ◽

World Health ◽

Control Group ◽

Life Questionnaire ◽

Myrtus Communis ◽

World Health Organization Quality ◽

Randomized Controlled ◽

Significant Difference

Abstract Introduction Due to the effects of hemorrhoids on physical and mental health, this study aimed to compare the effect of Myrtus communis herbal and anti-hemorrhoid ointments on symptoms of hemorrhoid and quality of life (primary outcomes) and satisfaction of the treatment and side effects (secondary outcomes). Methods This triple-blind randomized controlled trial was performed on women with grade I and II hemorrhoid referring to health centers in Tehran, Iran, in 2017. Individuals were randomly assigned to two groups of 67 people through block randomization method. The intervention group received the Myrtus communis herbal ointment and the control group received anti-hemorrhoid ointment twice a day, every 12 ± 2 h, an applicator of the drug through the rectum for 4 weeks. The Colorectal Evaluation of a Clinical Therapeutics Scale (CORECTS) was used to assess the severity of symptoms of hemorrhoid. To assess the quality of life, the World Health Organization Quality of Life questionnaire (WHOQOL-BREF) was used to measure the general quality of life of participants. This questionnaire was completed once before the start of the study, then on the fourth and the eighth week after the start of the intervention. Repeated measure ANOVA, Chi-square, Mann–Whitney U and independent t-test were used for data analysis. Results The severity of all symptoms of hemorrhoid decreased in both two group and there was no statistically significant difference between the two groups (p>0.05). However, the mean of anal itching at 4 and 8 weeks after the intervention was significantly lower in the Myrtus communis ointment group (p<0.05). There was no significant difference between groups in terms of quality of life at 4 and 8 weeks after the intervention (p>0.05). There was a significant difference between the two groups in terms of satisfaction with the drug (p=0.019) and the participants in the Myrtus communis ointment group were more satisfied with their drug use. Conclusions Myrtus communis herbal ointment was able to reduce the symptoms of hemorrhoid in the affected women. Therefore, it is likely that the use of this drug will promote the health of mothers with hemorrhoid.

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Decreased anxiety after Dawood fasting in the pre-elderly and elderly

Journal of Complementary and Integrative Medicine ◽

10.1515/jcim-2017-0172 ◽

2018 ◽

Vol 16 (1) ◽

Cited By ~ 3

Author(s):

Ika Fidianingsih ◽

Nur Aisyah Jamil ◽

Russy Novita Andriani ◽

Wira Muhammad Rindra

Keyword(s):

Quality Of Life ◽

Rating Scale ◽

Ketone Bodies ◽

The Elderly ◽

World Health Organisation ◽

World Health ◽

Control Group ◽

Control Group Design ◽

Significant Difference

Abstract Background A high prevalence of anxiety in the elderly often leads to decreased quality of life (QOL). A restrictive diet can increase the production of ketone bodies that encourage mood enhancement, neural protection and pain reduction. This study aimed to identify whether Dawood fasting could increase the QOL of the elderly by reducing anxiety. Methods This research was a quasi-experimental study involving a pretest–post-test control group design. The subjects were pre-elderly and elderly or healthy people aged more than 50, and a consecutive sampling method was employed. The fasting group observed the fast of Dawood, in which they abstained from eating, drinking, or having sexual intercourse from the break of dawn to dusk with the expressed intent to fast every other day. The fast was observed for 22 days (11 fasting days). Anxiety was examined using the Hamilton Rating Scale for Anxiety (HRS-A), while QOL was identified using the Indonesian version of the World Health Organisation Quality of Life (WHOQOL). Results A total of 48 respondents participated in this study with 24 respondents observing the fast of Dawood and 24 others not fasting. Results showed that the 22 days of Dawood fast reduced respondents’ complaints about anxiety by 4.37% and was significantly different from the non-fasting group (p=0.001). There was an increase in the QOL of the fasting group (p=0.019), although no significant difference was found when compared to the non-fasting group. Conclusions The fast of Dawood reduced anxiety in the pre-elderly and elderly.

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Relationship between Quality of Life and Occupational Accidents in South-East of Iran (Zahedan)

Global Journal of Health Science ◽

10.5539/gjhs.v9n2p112 ◽

2016 ◽

Vol 9 (2) ◽

pp. 112 ◽

Cited By ~ 1

Author(s):

Fereydoon Laal ◽

Mohammad Jafari Modrek ◽

Davoud Balarak ◽

Mahdi Mohammadi ◽

Mahdieh Rakhshani ◽

...

Keyword(s):

Quality Of Life ◽

Psychological Health ◽

Statistical Significance ◽

Occupational Accidents ◽

Control Group ◽

Life Questionnaire ◽

Significant Difference ◽

The Mean ◽

And Control

With the development of science and technology, occupational accidents, as one of the most important problems in the world, result in negative effects on physical and psychological health, and also the quality of life of workers. The aim of this study was to compare the quality of life among workers with and without accident. In a cross-sectional study, 93 workers were selected, 31 who experienced accident and 62 as control group. To gather the data, a researcher-made questionnaire for demographic characteristics and the quality of life questionnaire (SF-36) were used. Mann-Whitney and Chi-square tests were used for data analysis. The mean and standard deviation of age was 30.81±7.29 and 30.56±7.19 in workers with accident (case group) and control group, respectively. Homogeneity was ensured in terms of age and work experience and the two groups had no significant difference in this regard (p>0.05). Most of the participants were high school graduates (67.7%). The majority of accidents (68.8%) had occurred in the manufacturing sections. The most common accident type was sprayed chemical substances (19.4%) and the less frequent was electrocution (3.2%). The mean total score for the quality of life was 37.61±14.29 and 74.92±12.95 in the case and control groups with a statistical significance difference (p<0.001). The results of this study indicate that the incident could affect the quality of life of workers. Therefore, promoting the safety culture can help to reduce the occupational accidents.

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Effects of a Few Minutes of Abdominal Drawing-in Maneuver on Balance Test Results

10.32592/ircmj.2021.23.5.774 ◽

2021 ◽

Keyword(s):

Quality Of Life ◽

Repeated Measures ◽

Controlled Trial ◽

Intervention Group ◽

Educational Interventions ◽

Control Group ◽

Life Questionnaire ◽

Menopausal Women ◽

Significant Difference

Background: Menopause is a natural part of women's lives and is associated with a series of complications that can impair their quality of life. This study was conducted to determine the effect of educational interventions based on the Multi-Theory Model (MTM) on the quality of life among menopausal women. Methods: This randomized controlled trial was conducted on 80 menopausal women who met the inclusion criteria and were selected through the multi-stage stratified random sampling method. The participants were randomly allocated to either the control or intervention group (40 subjects per group). The intervention group participated in five 45-min educational sessions based on the MTM on the predetermined days of the week. The quality of life level scores were collected at baseline, immediately, and three months after the intervention using the Menopause-Specific Quality of Life questionnaire (MENQOL). On the other hand, the control group did not receive any intervention during the study period. Results: Analysis of variance of repeated measures showed a significant interaction between time and intervention. Therefore, the independent t-test was used to compare the mean score of quality of life, before, immediately, and three months after the intervention. The results showed a significant difference between the two groups regarding the scores immediately after and three months after the intervention. Conclusion: Structured educational program based on the MTM could be used as a simple and noninvasive intervention that helps menopausal women’s general health through menopausal symptoms relief, thereby improving their quality of life. Further interventions with larger sample sizes may be required to confirm these findings.

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Mobile Health in Supporting the Elderly Caregivers: A Non-Randomized Controlled Pilot Study (Preprint)

10.2196/preprints.15627 ◽

2019 ◽

Author(s):

Tzu-Ning Wen ◽

Tzu-Hui Hsia ◽

Po-Liang Cheng ◽

Qi-Guang Chen ◽

Hsiu-Yen Huang ◽

...

Keyword(s):

Quality Of Life ◽

Home Care ◽

Family Caregivers ◽

Mobile Health ◽

Physiological Data ◽

Control Group ◽

Life Questionnaire ◽

Middle Aged ◽

Significant Difference

BACKGROUND As the population of Taiwan continues to age rapidly, middle-aged and elderly people will increasingly begin to care for their older relatives. Therefore, the responsibility and complexity of care required from family caregivers will increase. The mobile health technology (mHealth) model has been successfully applied to numerous care services. OBJECTIVE To develop a mobile health app that supports family caregivers of various ages by meeting their home care needs, thus improving their quality of life, decreasing their severity of depression, and making them more empowered. METHODS This study applied a nonrandomized control-group pretest–posttest design. Purposive sampling was employed to recruit 30 family caregivers—16 middle-aged and 14 old family caregivers—from the home care cases of a regional hospital in Taipei. The developed home care mHealth app was used for management and monitoring of patient health. The outcomes measured were quality of life, level of depression, and sense of empowerment. RESULTS The results indicated that use of the mHealth app improved the technology acceptance, quality of life, depression level, and empowerment of the family caregivers. The old caregivers obtained quality of life scores that were 2.23 points higher, on average, than those obtained by the middle-aged caregivers P = .01, a significant difference. On the quality of life questionnaire, the old caregivers’ obtained scores for the health and family factors that were 2.75 P = .01 and 2.49 P = .01 points higher, respectively, than those obtained by the middle-aged caregivers, indicating significant differences. Regarding empowerment and depression, the scores obtained at different time points indicated that both groups became more empowered and less depressed over time, but no significant differences were discovered between the two groups. CONCLUSIONS According to our results, using the home care mHealth app had a positive influence the app is concluded to be a favorable tool for care education and management. Old caregivers found the software useful for managing patients’ physiological data, and they wished that other assistive methods were available to help them understand the internal functions. The software contributes to quality of life improvement, a decrease in depression severity, and empowerment enhancement and can be used by family caregivers as a reference for home care management in the future.

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Efficacy and Safety of Electro-Acupuncture (EA) on Insomnia in Patients with Lung Cancer: Study Protocol of a Randomized Controlled Trial

10.21203/rs.3.rs-20546/v1 ◽

2020 ◽

Author(s):

Hongyu Yue ◽

Shuang Zhou ◽

Huangan Wu ◽

Xuan Yin ◽

Shanshan Li ◽

...

Keyword(s):

Quality Of Life ◽

Lung Cancer ◽

Cancer Survivors ◽

Primary Outcome ◽

Controlled Trial ◽

Control Group ◽

Life Questionnaire ◽

Efficacy And Safety ◽

Secondary Outcomes

Abstract Background : Cancer-related insomnia (CRI) is one of the most prevalent complaints among cancer survivors and severely impairs patients’ quality of life. As a popular non-pharmacological alternative treatment, acupuncture provides a good clinical curative effect on insomnia. The aim of this trial is to evaluate efficacy and safety of electro-acupuncture on insomnia in patients with lung cancer. Method : This is a protocol for a multicenter randomized single-blinded sham-controlled trial. We will randomly assign 252 eligible patients with lung cancer-related insomnia into two groups at a ratio of 1:1, the treatment group (EA) and the control group (sham EA). All treatment will be given 3 times per week for 8 weeks, and a 12-week follow-up will be conducted. The primary outcome will be measured by the Pittsburgh Sleep Quality Index (PSQI). The secondary outcomes will include sleep parameters recorded from the actigraphy, scores from Quality of Life Questionnaire Core-30 (QLQ-C30), and Patient Health Questionnaire-9 (PHQ-9). All adverse effects during the trial will be assessed by the Treatment Emergent Symptom Scale (TESS). The primary outcome will be assessed at baseline, week 4, week 8, week 12 and week 20. The secondary outcomes will only be assessed at baseline and week 8. Discussion : This large-sample trial protocol will evaluate the efficacy of electro-acupuncture on insomnia in patients with lung cancer. This protocol, if proven to be effective, will contribute to filling the gap in treatment options in the CRI field and provide a promising intervention for insomnia in lung cancer survivors. Trial registration: ChiCTR, ChiCTR1900026395, Registered 8 October 2019, http://www.chictr.org.cn/showproj.aspx?proj=44068

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Efficacy and Safety of Electro-Acupuncture (EA) on Insomnia in Patients with Lung Cancer: Study Protocol of a Randomized Controlled Trial

10.21203/rs.3.rs-20546/v2 ◽

2020 ◽

Author(s):

Hongyu Yue ◽

Shuang Zhou ◽

Huangan Wu ◽

Xuan Yin ◽

Shanshan Li ◽

...

Keyword(s):

Quality Of Life ◽

Lung Cancer ◽

Cancer Survivors ◽

Controlled Trial ◽

Control Group ◽

Life Questionnaire ◽

Efficacy And Safety ◽

Symptom Scale ◽

Significance Level

Abstract Background: Cancer-related insomnia (CRI) is one of the most prevalent complaints among cancer survivors and severely impairs patients’ quality of life. As a popular non-pharmacological alternative treatment, acupuncture provides a good clinical curative effect on insomnia. The aim of this trial is to evaluate efficacy and safety of electro-acupuncture on insomnia in patients with lung cancer. Method: This is a protocol for a multicenter randomized single-blinded sham-controlled trial. We will randomly assign 252 eligible patients with lung cancer-related insomnia into two groups at a ratio of 1:1, the treatment group (EA) and the control group (sham EA). All treatment will be given 3 times per week for 8 weeks, and a 12-week follow-up will be conducted. The primary outcome will be measured by the Pittsburgh Sleep Quality Index (PSQI). The secondary outcomes will include sleep parameters recorded from the actigraphy, scores from Quality of Life Questionnaire Core-30 (QLQ-C30), and Patient Health Questionnaire-9 (PHQ-9). All adverse effects during the trial will be assessed by the Treatment Emergent Symptom Scale (TESS). All analyses will be based on ITT principle and performed with the statistical software SPSS (version 24.0) by t test, rank-sum test, chi-square and so on. A two-sided significance level will be set at 5%.Discussion: This large-sample trial protocol will evaluate the efficacy of electro-acupuncture on insomnia in patients with lung cancer. This protocol, if proven to be effective, will contribute to filling the gap in treatment options in the CRI field and provide a promising intervention for insomnia in lung cancer survivors. Trial registration: ChiCTR, ChiCTR1900026395, Registered 8 October 2019, http://www.chictr.org.cn/showproj.aspx?proj=44068

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A Comparative Study of Quality of Life in Infertile and Fertile Women Referred to Jahrom Infertility Clinics

Global Journal of Health Science ◽

10.5539/gjhs.v9n4p174 ◽

2016 ◽

Vol 9 (4) ◽

pp. 174

Author(s):

Razieh Parnian ◽

Farzad Poorgholami ◽

Nehle Parandavar ◽

Safeih Jamali ◽

Fatemeh Shakeri

Keyword(s):

Quality Of Life ◽

Social Life ◽

World Health ◽

Control Group ◽

Case Group ◽

Life Questionnaire ◽

World Health Organization Quality ◽

Infertile Women ◽

Significant Difference

INTRODUCTION: Infertility is a medical problem which influences all the dimensions of one’s individual and social life and can expose him/her to psycho-physical, socio-economic, sexual and family challenges. This study was designed to compare the quality of life of fertile and infertile women.MATERIALS & METHODOLOGY: This is a case-control analytical study in which 180 fertile and infertile women (aged 18-42) participated. The infertile group consisted of women who had visited an infertility treatment clinic. The fertile group consisted of healthy women who had children and had visited a healthcare center in the city of Jahrom. For the case group (n=90), sampling was conducted based on the census method; for the control group (n=90), subjects were selected through stratified random sampling. Data were collected using a questionnaire which had two sections: demographic information and the World Health Organization quality of life questionnaire (WHO QOL-BREF). The collected data were analyzed using SPSS version 16.RESULTS: The mean age of the participants was 28.26±4.85 years. 76.5% of the infertility cases were due to female infertility and 5.9% were due to male infertility. The results showed that there was a significant difference between the infertile and fertile groups in their overall satisfaction with life levels (p=0.002). There were no significant differences between the two groups in mean scores of somatic, psychological, social and environmental dimensions (p>0.05).CONCLUSION: Considering the results of the present research, it seems that factors like acceptance of infertility by couples, hope for present medical solutions to be effective, use of support plans and recent advancements in technology are possible reasons for the absence of difference between the infertile and fertile groups in quality of life.

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THE IMPACT OF OVERWEIGHT AND OBESITY ON THE QUALITY OF LIFE IN CHILDREN WITH BRONCHIAL ASTHMA

Wiadomości Lekarskie ◽

10.36740/wlek202006111 ◽

2020 ◽

Vol 73 (6) ◽

pp. 1140-1144

Author(s):

Anna V. Kupkina ◽

Oleksandr P. Volosovets ◽

Sergii P. Kryvopustov ◽

Marija P. Prokhorova ◽

Olena V. Mozyrska

Keyword(s):

Quality Of Life ◽

Bronchial Asthma ◽

Rating Scale ◽

Overweight And Obesity ◽

The Body ◽

Life Questionnaire ◽

Laboratory Assessment ◽

Significant Difference ◽

The Impact

The aim is to investigate if the overweight (OW) and obesity (OB) impact on the quality of life (QOL) of children with bronchial asthma (BA). Materials and methods: The study included 73 children aged 7 – 17, with moderate BA. Depending on the body mass index, patients were divided into the three clinical groups: normal body weight (NW) – 30 children, OW – 28 children and OB – 15 children. QOL was conducted by the Pediatric Asthma Quality of Life Questionnaire (PAQLQ). The statistical processing was carried out using the IBM SPSS Statistics Base (version 22) and EZR version 1.32. Results were considered statistically significant when p<0.05. Results: Children with BA and OB had statistically lower QOL than children with BA and NW in all PAQLQ domains. The Kruskal-Wallis H-test revealed a statistically significant difference between the different weight groups of children with BA both for the general QOL: H(2) = 37.51, p<0.001and for each rating scale separately. Pairwise comparisons using Steel-Dwass test indicated that scores of NW were observed to be significantly different from those of OW and OB for rating Activity and Symptoms scales (p<0.001). Conclusion: Comorbid OW and OB reduce the specific QOL of children with BA. In assessing the effectiveness of specific approaches to treating BA in children with OW and OB, an assessment of the QOL of children should be added to the traditional common clinical and laboratory assessment.

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