| Literature DB >> 25701663 |
Desiree G M van den Hurk1, Melanie P J Schellekens2, Johan Molema2, Anne E M Speckens2, Miep A van der Drift2.
Abstract
BACKGROUND: Lung cancer patients and partners show high rates of impaired quality of life and heightened distress levels. Mindfulness-Based Stress Reduction has proven to be effective in reducing psychological distress in cancer patients. However, studies barely included lung cancer patients. AIM: We examined whether Mindfulness-Based Stress Reduction might be a feasible and effective intervention for patients with lung cancer and partners.Entities:
Keywords: Mindfulness-Based Stress Reduction; lung cancer; mindfulness; partners; psychological distress
Mesh:
Year: 2015 PMID: 25701663 PMCID: PMC4457793 DOI: 10.1177/0269216315572720
Source DB: PubMed Journal: Palliat Med ISSN: 0269-2163 Impact factor: 4.762
Figure 1.Topic list of semi-structured interview.
Clinical and psychological characteristics among patients and partners at baseline.
| Clinical characteristics | Patients | Partners | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Total ( | Completers ( | Non-completers ( | Total ( | Completers ( | Non-completers ( | |||||||
| Age, mean (range) | 61.7 | (54–77) | 62.2 | (54–77) | 59 | (57–62) | 60.9 | (30–76) | 59.8 | (30–76) | 65.0 | (61–68) |
| Female gender, | 9 | (47) | 7 | (44) | 2 | (67) | 9 | (56) | 9 | (69) | 0 | (0) |
| Cancer type, | ||||||||||||
| Non-small cell lung cancer | 15 | (79) | ||||||||||
| Small cell lung cancer | 4 | (21) | ||||||||||
| Cancer stage, | 4/15 | (21/79) | ||||||||||
| I | 0 | (0) | 0 | (0) | 0 | (0) | ||||||
| IIa | 2 | (11) | 2 | (12) | 0 | (0) | ||||||
| IIb | 0 | (0) | 0 | (0) | 0 | (0) | ||||||
| IIIa | 3 | (16) | 3 | (19) | 0 | (0) | ||||||
| IIIb | 3 | (16) | 2 | (12) | 1 | (33) | ||||||
| IV | 11 | (58) | 9 | (56) | 2 | (67) | ||||||
| Treatment(s) during MBSR, | 14 | (74) | 11 | (69) | 3 | (100) | ||||||
| Chemotherapy | 11 | (58) | 9 | (56) | 2 | (67) | ||||||
| Radiation | 2 | (11) | 1 | (6) | 1 | (33) | ||||||
| Chemotherapy and radiation | 1 | (5) | 1 | (6) | 0 | (0) | ||||||
| Time since diagnosis (in months), mean (range) | 8.4 | (2–35) | 9.0 | (2–35) | 5.3 | (3–9) | ||||||
| Psychological distress (HADS), mean (SD) | 14.7 | (5.6) | 14.6 | (6.1) | 15.7 | (2.9) | 17.7 | (7.8) | 18.5 | (8.1) | 14.1 | (5.3) |
| Anxiety | 7.8 | (2.9) | 7.9 | (3.1) | 7.7 | (2.3) | 9.9 | (5.0) | 10.3 | (5.1) | 8.0 | (3.5) |
| Depression | 6.8 | (3.6) | 6.7 | (3.8) | 8.0 | (2.6) | 7.8 | (3.3) | 8.2 | (3.4) | 6.1 | (1.8) |
| Quality of life (QLQ-LC13), mean (SD) | ||||||||||||
| Dyspnoea | 5.5 | (2.0) | 5.7 | (2.1) | 4.3 | (1.5) | ||||||
| Coughing | 1.8 | (0.9) | 1.9 | (0.9) | 1.3 | (0.6) | ||||||
| Haemoptysis | 1.2 | (0.5) | 1.2 | (0.5) | 1 | (0.0) | ||||||
| Pain | 4.9 | (1.5) | 4.9 | (1.3) | 5 | (2.6) | ||||||
| Fatigue (CIS-F) | 37.8 | (12.0) | 36.6 | (12.0) | 46.5 | (0.7) | ||||||
| Distress thermometer, mean (SD), | 4.3 | (1.97) | ||||||||||
| Caregiver burden (SPPIC), mean (SD) | 24.9 | (6.0) | 25.2 | (5.6) | 19 | (5.7) | ||||||
MBSR: Mindfulness-Based Stress Reduction; HADS: Hospital Anxiety and Depression Scale; SD: Standard Deviation; QLQ-LC13: Quality-of-Life Questionnaire–Lung Cancer 13; SPPIC: Self-Perceived Pressure from Informal Care; CIS-F: Checklist Individual Strength–Fatigue.
Baseline, post and follow-up scores of patients and partners.
| Patient | Partner | |||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Baseline ( | Post ( | Follow-up ( | Baseline ( | Post ( | Follow-up ( | |||||||
| Mean | (SD) | Mean | (SD) | Mean | (SD) | Mean | (SD) | Mean | (SD) | Mean | (SD) | |
| Psychological distress (HADS) | 13.2 | (5.9) | 12.7 | (5.7) | 11.8 | (7.7) | 18.6 | (9.1) | 15.6 | (7.0) | 16.8 | (8.8) |
| Anxiety | 7.1 | (2.4) | 6.2 | (2.7) | 5.6 | (3.8) | 10.6 | (6.8) | 9.4 | (4.0) | 9.8 | (4.0) |
| Depression | 6.2 | (4.0) | 6.5 | (3.9) | 6.2 | (4.3) | 8.1 | (3.9) | 6.3 | (3.6) | 7.0 | (5.0) |
| Quality of life (QLQ-LC13) | ||||||||||||
| Dyspnoea (items 3,4,5) | 5.9 | (1.9) | 6.1 | (2.1) | 7.0 | (2.8) | ||||||
| Coughing (item 1) | 2.0 | (0.9) | 2.1 | (1.0) | 2.3 | (0.9) | ||||||
| Haemoptysis (item 2) | 1.2 | (0.6) | 1.2 | (0.4) | 1.0 | (0.0) | ||||||
| Pain (items 10, 11, 12) | 5.0 | (1.2) | 4.7 | (1.9) | 4.4 | (1.7) | ||||||
| Fatigue (CIS-F) | 35.9 | (13.0) | 33.6 | (13.1) | 34.9 | (11.2) | ||||||
| Psychological stress reaction (IES) | ||||||||||||
| Intrusive experiences | 20.2 | (7.8) | 21.7 | (5.1) | 21.2 | (4.1) | ||||||
| Avoidance of thoughts | 10.7 | (4.1) | 11.9 | (3.4) | 10.1 | (2.8) | ||||||
| (Worry) PSWQ | 44.5 | (15.0) | 41.1 | (12.3) | 38.8 | (6.8) | 47.1 | (10.0) | 40.6 | (17.2) | 43.3 | (8.3) |
| (Awareness) MAAS | 67.5 | (14.4) | 65.1 | (7.9) | 67.8 | (7.7) | 64.0 | (10.7) | 59.6 | (11.7) | 60.9 | (12.2) |
| Caregiver burden (SPPIC) | 28.0 | (3.6) | 23.2 | (3.8) | 21.1 | (3.9) | ||||||
| Caregiver self-esteem (CRA-SE) | 30.2 | (2.2) | 30.0 | (2.4) | 30.6 | (2.3) | ||||||
SD: standard deviation; HADS: Hospital Anxiety and Depression Scale; QLQ-LC13: Quality of Life Questionnaire–Lung Cancer 13; CIS-F: Checklist Individual Strength–Fatigue; IES: Impact of Event Scale; PSWQ: Penn State Worry Questionnaire; MAAS: Mindful Attention and Awareness Scale; SPPIC: Self-Perceived Pressure from Informal Care; CRA-SE: Caregiver Reaction Assessment–Care-derived Self-Esteem.
p < 0.05; **p < 0.01.
Qualitative themes of facilitators and barriers and corresponding quotations of patients and partners.
| Examples of facilitators | Examples of barriers | |
|---|---|---|
| Physical functioning | I liked the variety of exercises and could participate in all of them. (Patient) | There was a point in the exercise where I couldn’t keep up, and that was quite confronting, because a number of physical things, simple things, I couldn’t do anymore. (Patient) |
| Participating in a group | It gave me a liberating feeling to see that the others all had the same problem, you’re not alone, there are other people that have cancer. (Partner) | And then you start to think, ‘is it my turn now?’, that’s a big setback. (Patient) |
| Participating with partner | I heard how he dealt with it during the day, and that was nice. (Partner) | I couldn’t relax because I thought, he feels completely short of breath. (Partner) |
Qualitative themes of the process of change and corresponding quotations of patients and partners.
| Positive examples | Negative examples | |
|---|---|---|
| 1. Standing still | I got a more peaceful feeling more relaxed, a clearer mind. I always left with a good feeling. (Patient) | I couldn’t relax at all. (Partner) |
| 2. Being aware | What do you do that you like and what do you do that you don’t like; how do you react to this and how could you react. Yeah, that’s what you do and what you notice. (Partner) | I don’t want to be continually reminded of it. A couple of weeks ago I thought, ‘I do have this disease, but I don’t feel anything’. I especially think that on good days. But then ten people say, ‘Yes, you are sick’. That is very difficult. (Patient) |
| 3. Insight | Especially since I notice from myself that I tend to go on as if there’s nothing wrong. Just to feel as little as possible, because that makes it easier, no matter how difficult the situation is. (Partner) | |
| 4. Letting go | That I can let go of more things, that I shouldn’t be occupied with it. That I think, ‘not now’. I used to be ‘go, go, go’ – I now have the peace so that I don’t have to rush. (Patient) | As long as you’re together, you’re together. I don’t leave him home alone. No, others might think completely different about it. A bystander says, ‘You should do other things’. I do that – I go shopping and go to friends. But to say now, ‘I’d like to go away for a few days’, no, then I wouldn’t be at ease. (Partner) |
| 5. Changing behaviour | There came a time when it helped me to talk with my wife about it. It also got easier to talk with my children about it. […] That is a real joy. I can expose my feelings to my wife and vise versa. (Patient) | I can’t change myself anymore. It was also in the training: you have to do this, you have to do that … but it doesn’t work that way. My age probably plays a role – they say, ‘You have to do this’, but I don’t have to do anything. (Patient) |
| 6. Acceptance | I can’t do much physically anymore. At the time, that was quite confronting, but that’s more than a half a year ago. There comes a time when you just have to accept it when it happens. (Patient) | If I’ve been awake for a half hour, then I know how my day will be. Will it be good or will I be extremely tired again. If I’m tired, then I just go from couch to couch (bench to bench). Then I get very angry at not being able to do anything. (Patient) |