The Influence of the Bmgim Music Therapy Method in the Reduction of Stress in Patients With Inflammatory Bowel Disease (Crohn's Disease and Ulcerative Colitis): Quantitative and Qualitative Study
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 51
- 试验地点
- 2
- 主要终点
- Change in Hospital Anxiety and Depression Scale (HADS) (PRE and POST Measures)
研究概览
简要总结
Inflammatory bowel disease (IBD) is a term that defines a chronic disease characterized by inflammation of the intestine. It includes ulcerative colitis (UC) and Crohn's disease (CD). The objective of the study was to administer a treatment based on a group adaptation of the BMGIM in patients with inflammatory bowel disease (IBD) and assess its impact on state of mind, quality of life, anxiety, depression, immunocompetence as a marker of well-being, and levels of acute and chronic stress.
To achieve the objectives a quasi-experimental, quantitative, qualitative, analytical, and prospective study was performed. 41 patients with IBD divided into a test group (24 patients), who received 8 sessions over 8 weeks, and a control group (17 patients). A saliva sample was taken from each patient before and after each session to determine cortisol levels (acute stress) and IgA (immunocompetence) using ELISA. A series of questionnaires were completed as follows: HADS (perceived anxiety), MOOD (state of mind), and CCVEII (quality of life). Similarly, a hair sample was taken before the first and after the last session to determine the cumulative cortisol level (chronic stress) using ELISA.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 20 Years 至 69 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Over 18 years old,
- •Diagnosed IBD (EC or UC) in the remission phase,
- •They did not receive treatment with corticosteroids at least in the two months prior to the start of the study,
- •They did not receive any extra pharmacological treatment,
- •Attend the collaborating hospital center with the study, in this case, the University General Hospital of Valencia,
- •Attend the schedule and schedule established for the study,
- •Accept the conditions of participation in the study indicated in the signed informed consent prior to the start of the study
- •* Do not take corticosteroids during the 8 weeks between the pre-test and the post-test,
- •* Perform the pre-test before starting session 1 (in case of experimental group) or appointment 1 (in case of control group); and then the retest at the end of session 8 (in the case of an experimental group) or appointment with nursing after 8 weeks (in the case of a control group).
- •* In the case of the patients belonging to the experimental group, who at the end of the 8 weeks of treatment would have attended at least 6 of the 8 sessions established (and that, obligatorily, 2 of them were 1 and 8, where the shots were taken) sample and completed the questionnaires).
排除标准
- •The patients who were excluded from this study were those who did not meet the requirements indicated in the inclusion criteria, or who showed aversion or rejection to this type of therapy.
研究组 & 干预措施
Control Group
Experimental Group
干预措施: BMGIM Music Therapy Method (Other)
结局指标
主要结局
Change in Hospital Anxiety and Depression Scale (HADS) (PRE and POST Measures)
时间窗: Baseline up to 8 weeks of treatment
14 items. 7 items for Anxiety and 7 for Depression. The score for the items is evaluated on a Likert scale ranging from 0 to 3 points, where 0 represents never or almost never, 1 a little or from time to time, 2 somewhat less than before or not as intense, and 3 maximum or almost always. Lastly, it is worth mentioning that these scales are interpreted based on the sum of each dimension, with 21 as the maximum, both for depression and for anxiety. Higher values represent a worse outcome. Observing change comparing pre and post intervention
Change in Short-form Questionnaire on Quality of Life in IBD (CCVEII-9) (PRE and POST Measures)
时间窗: Baseline up to 8 weeks of treatment
9 items grouped in a single dimension The final score is expressed on a scale of 0 to 100 points, such that a lower score corresponds to a lower quality of life and vice versa. Observing change comparing pre and post intervention
Change in the MOOD questionnaire (PRE and POST Measures).
时间窗: Baseline up to 8 weeks of treatment
The scale evaluates the frequency of the different states of mind (happiness, anger, sadness, and fear) based on 20 items (4 dimensions of 5 items each). The responses for the items were measured using a 3-point Likert scale (1=never, 2=sometimes, 3=often). Each dimension range from 1 to 3. There is not a total of all dimensions together. a lower score corresponds to high level fo that mood (lower values= a betwer outcome on anger, sadness, and fear and worst outcome on hapiness). Observing change comparing pre and post intervention
Change in biological markers in saliva samples using enzyme-linked immunosorbent biological markers assay (ELISA) (PRE and POST Measures).
时间窗: Baseline up to 8 weeks of treatment
Quantifying change in biological markers in saliva samples using enzyme-linked immunosorbent assay (ELISA). (IgA level \& Salivary Cortisol) comparing pre and post intervention
Change in biological markers in hair using enzyme-linked immunosorbent assay (ELISA).(PRE and POST Measures).
时间窗: Baseline up to 8 weeks of treatment
Quantifying change in biological markers in hair (Cortisol Hair) comparing pre and post intervention
次要结局
未报告次要终点
研究者
Vicente J Prado Gascó
Profesor Ayudante Doctor
University of Valencia