597 related articles for article (PubMed ID: 29530909)
1. Understanding the role of health information in patients' experiences: secondary analysis of qualitative narrative interviews with people diagnosed with cancer in Germany.
Blödt S; Kaiser M; Adam Y; Adami S; Schultze M; Müller-Nordhorn J; Holmberg C
BMJ Open; 2018 Mar; 8(3):e019576. PubMed ID: 29530909
[TBL] [Abstract][Full Text] [Related]
2. Using others' experiences. Cancer patients' expectations and navigation of a website providing narratives on prostate, breast and colorectal cancer.
Engler J; Adami S; Adam Y; Keller B; Repke T; Fügemann H; Lucius-Hoene G; Müller-Nordhorn J; Holmberg C
Patient Educ Couns; 2016 Aug; 99(8):1325-32. PubMed ID: 27067064
[TBL] [Abstract][Full Text] [Related]
3. Palliative care experiences of adult cancer patients from ethnocultural groups: a qualitative systematic review protocol.
Busolo D; Woodgate R
JBI Database System Rev Implement Rep; 2015 Jan; 13(1):99-111. PubMed ID: 26447011
[TBL] [Abstract][Full Text] [Related]
4. Are there also negative effects of social support? A qualitative study of patients with inflammatory bowel disease.
Palant A; Himmel W
BMJ Open; 2019 Jan; 9(1):e022642. PubMed ID: 30670504
[TBL] [Abstract][Full Text] [Related]
5. The experiences of family members in the year following the diagnosis of a child or adolescent with cancer: a qualitative systematic review.
Mu PF; Lee MY; Sheng CC; Tung PC; Huang LY; Chen YW
JBI Database System Rev Implement Rep; 2015 Jun; 13(5):293-329. PubMed ID: 26455612
[TBL] [Abstract][Full Text] [Related]
6. Trust, medical expertise and humaneness: A qualitative study on people with cancer' satisfaction with medical care.
Blödt S; Müller-Nordhorn J; Seifert G; Holmberg C
Health Expect; 2021 Apr; 24(2):317-326. PubMed ID: 33528878
[TBL] [Abstract][Full Text] [Related]
7. Learning-by-doing: the importance of experiential knowledge sharing for meeting the information needs of people with colorectal cancer in Germany-a qualitative study.
Kaiser M; Adami S; Lucius-Hoene G; Muller-Nordhorn J; Goerling U; Breuning M; Holmberg C
BMJ Open; 2021 Feb; 11(2):e038460. PubMed ID: 33622937
[TBL] [Abstract][Full Text] [Related]
8. Coping, meaning and symptom experience: a narrative approach to the overwhelming impacts of breast cancer in the first year following diagnosis.
Tighe M; Molassiotis A; Morris J; Richardson J
Eur J Oncol Nurs; 2011 Jul; 15(3):226-32. PubMed ID: 21511530
[TBL] [Abstract][Full Text] [Related]
9. Perceived barriers to and facilitators of being physically active during adjuvant cancer treatment.
Henriksson A; Arving C; Johansson B; Igelström H; Nordin K
Patient Educ Couns; 2016 Jul; 99(7):1220-1226. PubMed ID: 26860549
[TBL] [Abstract][Full Text] [Related]
10. Effect of a Website That Presents Patients' Experiences on Self-Efficacy and Patient Competence of Colorectal Cancer Patients: Web-Based Randomized Controlled Trial.
Giesler JM; Keller B; Repke T; Leonhart R; Weis J; Muckelbauer R; Rieckmann N; Müller-Nordhorn J; Lucius-Hoene G; Holmberg C
J Med Internet Res; 2017 Oct; 19(10):e334. PubMed ID: 29030329
[TBL] [Abstract][Full Text] [Related]
11. Coping mechanisms for financial toxicity: a qualitative study of cancer patients' experiences in Germany.
Schröder SL; Schumann N; Fink A; Richter M
Support Care Cancer; 2020 Mar; 28(3):1131-1139. PubMed ID: 31201545
[TBL] [Abstract][Full Text] [Related]
12. Coping Strategies Used by Breast, Prostate, and Colorectal Cancer Survivors: A Literature Review.
Lashbrook MP; Valery PC; Knott V; Kirshbaum MN; Bernardes CM
Cancer Nurs; 2018; 41(5):E23-E39. PubMed ID: 28723724
[TBL] [Abstract][Full Text] [Related]
13. Uncertainty in breast, prostate, and colorectal cancer: implications for supportive care.
Shaha M; Cox CL; Talman K; Kelly D
J Nurs Scholarsh; 2008; 40(1):60-7. PubMed ID: 18302593
[TBL] [Abstract][Full Text] [Related]
14. Coping with colorectal cancer: a qualitative exploration with patients and their family members.
Asiedu GB; Eustace RW; Eton DT; Radecki Breitkopf C
Fam Pract; 2014 Oct; 31(5):598-606. PubMed ID: 25080507
[TBL] [Abstract][Full Text] [Related]
15. The experience of adults who choose watchful waiting or active surveillance as an approach to medical treatment: a qualitative systematic review.
Rittenmeyer L; Huffman D; Alagna M; Moore E
JBI Database System Rev Implement Rep; 2016 Feb; 14(2):174-255. PubMed ID: 27536798
[TBL] [Abstract][Full Text] [Related]
16. Engaging in medical vigilance: understanding the personal meaning of breast surveillance.
Underhill ML; Dickerson SS
Oncol Nurs Forum; 2011 Nov; 38(6):686-94. PubMed ID: 22037331
[TBL] [Abstract][Full Text] [Related]
17. Meaning of living with severe chronic obstructive lung disease: a qualitative study.
Marx G; Nasse M; Stanze H; Boakye SO; Nauck F; Schneider N
BMJ Open; 2016 Dec; 6(12):e011555. PubMed ID: 27932338
[TBL] [Abstract][Full Text] [Related]
18. "I can't get it into my head that I have cancer…"-A qualitative interview study on needs of patients with lung cancer.
Stanze H; Schneider N; Nauck F; Marx G
PLoS One; 2019; 14(5):e0216778. PubMed ID: 31086395
[TBL] [Abstract][Full Text] [Related]
19. Comparing cancer experiences among people with colorectal cancer: a qualitative study.
McCaughan E; Parahoo K; Prue G
J Adv Nurs; 2011 Dec; 67(12):2686-95. PubMed ID: 21806670
[TBL] [Abstract][Full Text] [Related]
20. An in-depth exploration of information-seeking behavior among individuals with cancer: part 2: understanding patterns of information disinterest and avoidance.
Lambert SD; Loiselle CG; Macdonald ME
Cancer Nurs; 2009; 32(1):26-36. PubMed ID: 19104199
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]