| Literature DB >> 35585593 |
Titi Tran1, Bénédicte Clarisse1, Virginie Prevost2,3, Sophie Lefevre-Arbogast4,1,5, Alexandra Leconte1, Claire Delorme1, Sandrine Benoit1.
Abstract
BACKGROUND: Alleviating suffering and improving quality of life are universally shared goals. In this context, we implemented a pilot study to assess the feasibility and acceptability of a mindfulness intervention in the form of meditation involving together cancer patients, health professionals, and third persons.Entities:
Keywords: Cancer patients; Health professionals; Mindfulness; Pilot study; Well-being
Mesh:
Year: 2022 PMID: 35585593 PMCID: PMC9116698 DOI: 10.1186/s12906-022-03599-w
Source DB: PubMed Journal: BMC Complement Med Ther ISSN: 2662-7671
Eligibility criteria
| - Participants aged 18 or over |
| - Curious and motivated to participate in programme |
| - Participant with no current or previous experience of regular or intensive practice of meditation or |
| - comparable practice. Practice considered regular and / or intensive if: |
| • it occurs more than one day per week for more than 6 consecutive months over the last 10 years, |
| • and/or in case of more than 5 consecutive days of intensive practice (internship or retirement) in the last 10 years, |
| • and/or more than 25 consecutive days of (cumulative) retirement over the last 10 years |
| - Participant available to follow full meditation programme (3-month period) |
| - Participant agreeing to participate by signing study information note |
| - Participant able to understand, speak and read French |
| - Participant able to use digital media and having internet connection |
| - Patients with cancer |
| - State of health compatible with study meditation programme |
| - Patient affiliated to a French social insurance system |
| - All medical and/or paramedical health professionals of sponsor centre in contact with patients (doctors, nurses, nurse assistants, radiotherapy/radiology operatives…) |
| - Any voluntary person not belonging to the two categories above |
| - Participant with significant vulnerability factors: dependence on alcohol and drugs, severe depression, severe social anxiety, recent mourning etc.) |
| - Participant unable to participate for geographic, social or psychopathological reasons |
| - Participant deprived of liberty or under guardianship |
| - Very advanced stage of cancer disease with life-threatening symptoms |
| - Very advanced stage of cancer disease with life-threatening symptoms |
| - Health professional, regardless of their place of practice |
Fig. 1Study design
Fig. 2IMPLIC study flow chart
Sociodemographic characteristics of participants and meditation experience (N = 30)
| 60 (40–80) | 46 (30–60) | 57 (38–79) | 0.017 | 54 (30–80) | |
| 0.32 | |||||
| Female | 8 (80) | 10 (100) | 8 (80) | 26 (87) | |
| Male | 2 (20) | 0 (0) | 2 (20) | 4 (13) | |
| 0.079 | |||||
| Executives and higher intellectual | 4 (40) | 5 (50) | 7 (70) | 16 (53) | |
| profession | 1 (10) | 5 (50) | 2 (20) | 8 (27) | |
| Employees | 4 (40) | 0 (0) | 1 (10) | 5 (17) | |
| Intermediate occupation | 1 (10) | 0 (0) | 0 (0) | 1 (3) | |
| Other persons not in employment | |||||
| Nursing assistants | 1 (10) | ||||
| Doctor | 3 (30) | ||||
| Nurse | 1 (10) | ||||
| Radiotherapy/radiology operatives | 3 (30) | ||||
| Health executive | 2 (20) | ||||
| 0.32 | |||||
| Naive | 8 (80) | 10 (100) | 8 (80) | 26 (87) | |
| Sensitized | 2 (20) | 0 (0) | 2 (20) | 4 (13) |
P-values are from Kruskal–Wallis test for age and Chi-square tests for other categorical variables
Fig. 3Participants’ satisfaction per component (N = 28)
Each component of satisfaction was rated on a 5-point Likert scale from -2 (very dissatisfied) to + 2 (very satisfied). Radar charts display for each component the average satisfaction of participants in the total sample (left panel) and across the three groups (right panel). The zero line divides the scale from dissatisfaction to satisfaction. The closer the point to the centre of the axis, the larger the dissatisfaction; the closer the point to the end of the axis, the larger the satisfaction
Fig. 4Participants’ feeling about meditating together (N = 28)
Pre- and post-intervention exploratory outcome measures of participants (N = 28)
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|---|---|---|---|---|---|---|
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| 0–10 | 6.7 | 7.4 | 2.87 | 0.54 | 0.004 |
|
| 0-40c | 21 | 15 | 3.48 | 0.66 | < 0.001 |
|
| 14–56 | 35 | 38d | 3.28 | 0.62 | 0.001 |
| | 6–24 | 16 | 17d | 2.26 | 0.43 | 0.024 < 0.001 |
| | 8–32 | 20 | 22 | 3.42 | 0.65 | |
|
| ||||||
| | 7–35 | 25 | 27d | 0.89 | 0.17 | 0.37 |
| | 7–35 | 23 | 21d | 0.47 | 0.09 | 0.64 |
| | 7–35 | 31 | 31d | 0.51 | 0.10 | 0.61 |
| | 7–35 | 17 | 15d | 0.85 | 0.16 | 0.40 |
|
| 20–140 | 108d | 104d | 1.36 | 0.26 | 0.28 |
| | 57 | 54 | 1.70 | 0.32 | 0.090 | |
| | 10–70 | 46 | 43 | 1.54 | 0.29 | 0.12 |
| | 8–56 2–14 | 6.0d | 8.0d | 1.60 | 0.30 | 0.11 |
|
| 10–40 | 30 d | 33 | 3.51 | 0.66 | < 0.001 |
| | 9-63c | 33d | 28 | 0.68 | 0.26 | 0.50e |
| | 5-35c | 12d | 8 | 0.41 | 0.15 | 0.68e |
| | 8–56 | 41d | 51 | 1.44 | 0.54 | 0.15e |
a Effect sizes are computed as the ratio of the Z test statistic to the square root of the number of pairs and range from 0 to 1 with higher values indicating larger effect
b P-values are from paired Wilcoxon test comparing pre- and post-test scores
c High score indicates worse state
d Indicates 1 missing questionnaire, except for MBI (two missing baseline evaluations)
e P-value for pre-post comparison among health professionals only