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  • 1
    In: British Journal of Health Psychology, Wiley, Vol. 22, No. 3 ( 2017-09), p. 627-643
    Abstract: Most studies on fatigue in patients with cancer aggregate its prevalence and severity on a group level, ignoring the possibility that subgroups of patients may differ widely in their development of fatigue. This study aimed to identify subgroups of patients with clinically distinct trajectories of fatigue from diagnosis to 18 months post‐diagnosis. As fatigue might trigger goal disturbance, the study also identified trajectories of concrete and abstract goal disturbance and longitudinally examined their co‐occurrence with fatigue. Design Prospective design with quantitative and qualitative method of data collection. Methods Patients with colorectal cancer ( n  = 183) reported on their levels of fatigue and goal disturbance shortly after diagnosis ( T 1 ) and at 7 months ( T 2 ) and 18 months ( T 3 ) post‐diagnosis. Growth mixture model analyses were performed to identify trajectories of fatigue and goal disturbance. Guidelines for the clinical relevance of fatigue were applied. Results Four clinically distinct trajectories of fatigue were identified as follows: (1) persistent severe fatigue (25.4%), (2) moderate fatigue (56.1%), (3) no fatigue (13.8%), and (4) rapidly improving fatigue (4.7%). The majority of patients with cancer reported high disturbance of their concrete goals, while high disturbance of abstract goals was less evident. Fatigue and concrete goal disturbance co‐occurred longitudinally. Conclusions The fatigue and goal disturbance experienced from diagnosis to 18 months post‐diagnosis differ considerably for subgroups of patients with cancer. Fatigue and concrete goal disturbance are persistent burdens in the majority of patients. Investigating symptom burden beyond average trends can guide clinicians to identify patients most in need for treatment. Targeting goal disturbance might benefit the psychological well‐being in patients suffering from persistent symptoms. Statement of contribution What is already known on this subject? Fatigue is a common and distressing symptom at all stages of the cancer experience. Earlier studies suggest that many patients recover from fatigue after treatment completion. Patients with cancer experience disturbance in their personal goals, which is related to poor psychological well‐being. What does this study add? Developments of fatigue and goal disturbance differ between subgroups of patients with cancer but co‐occur within these subgroups. About 30% of the patients experience severe fatigue after diagnosis, of which only few patients recover within 18 months post‐diagnosis. Targeting goal disturbance might benefit patients with severe and ongoing symptoms.
    Type of Medium: Online Resource
    ISSN: 1359-107X , 2044-8287
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2017
    detail.hit.zdb_id: 2026500-1
    SSG: 5,2
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  • 2
    Online Resource
    Online Resource
    Mary Ann Liebert Inc ; 2018
    In:  Journal of Adolescent and Young Adult Oncology Vol. 7, No. 1 ( 2018-02), p. 72-78
    In: Journal of Adolescent and Young Adult Oncology, Mary Ann Liebert Inc, Vol. 7, No. 1 ( 2018-02), p. 72-78
    Type of Medium: Online Resource
    ISSN: 2156-5333 , 2156-535X
    Language: English
    Publisher: Mary Ann Liebert Inc
    Publication Date: 2018
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  • 3
    Online Resource
    Online Resource
    Mary Ann Liebert Inc ; 2022
    In:  Journal of Adolescent and Young Adult Oncology Vol. 11, No. 2 ( 2022-04-01), p. 138-145
    In: Journal of Adolescent and Young Adult Oncology, Mary Ann Liebert Inc, Vol. 11, No. 2 ( 2022-04-01), p. 138-145
    Type of Medium: Online Resource
    ISSN: 2156-5333 , 2156-535X
    Language: English
    Publisher: Mary Ann Liebert Inc
    Publication Date: 2022
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  • 4
    Online Resource
    Online Resource
    Mary Ann Liebert Inc ; 2017
    In:  Journal of Adolescent and Young Adult Oncology Vol. 6, No. 1 ( 2017-03), p. 134-141
    In: Journal of Adolescent and Young Adult Oncology, Mary Ann Liebert Inc, Vol. 6, No. 1 ( 2017-03), p. 134-141
    Type of Medium: Online Resource
    ISSN: 2156-5333 , 2156-535X
    Language: English
    Publisher: Mary Ann Liebert Inc
    Publication Date: 2017
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  • 5
    In: Psycho-Oncology, Wiley, Vol. 32, No. 6 ( 2023-06), p. 904-912
    Abstract: To describe young adult childhood cancer survivors' disclosure of their cancer history (i.e., disclosure behavior, difficulty, and timing), perceived partner responses, and associations with relationship status satisfaction. Methods German long‐term survivors of childhood cancer ( N  = 509; response rate: 31.3%, age 21–26, 59.7% female) completed a registry‐based nationwide survey (embedded mixed methods design, including closed and open‐ended questions) on measures about disclosure history (behavior, difficulty, and timing), partner responses, and relationship status satisfaction. Statistical ( χ 2 ‐, t ‐, or F ‐tests) and qualitative analyses were conducted. Results Half of all survivors always disclosed their cancer history to romantic partners. Thereby, three themes for considering (non‐)disclosure were identified: Survivors' attitudes, having integrated cancer as part of their identity, and anticipated effects on romantic relationships. About 40% indicated having no difficulties with disclosing their cancer history. The timing of disclosure varied, with most survivors disclosing after a few dates. Facilitators of disclosure were the visibility of their former illness (e.g., scars), having trust in a (potential) partner, getting older/mature, and previous positive experiences with disclosure. Few survivors (13.8%) had ever experienced negative responses from dating partners. Yet, those who had negative experiences, found it more difficult to disclose their cancer history. Survivors were overall rather satisfied with their relationship status, with partnered survivors reporting greater satisfaction than singles (Hedge's g  = 1.68); and particularly partnered survivors with past positive responses being most satisfied. Conclusions Young adult childhood cancer survivors appear rather open in disclosing their cancer history to (potential) romantic partners, and few experienced negative responses. Psycho‐educational programs may emphasize such findings in helping to prevent fear of disclosure or avoidance of dating and disclosure among survivors.
    Type of Medium: Online Resource
    ISSN: 1057-9249 , 1099-1611
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 1495115-0
    SSG: 5,2
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  • 6
    Online Resource
    Online Resource
    Frontiers Media SA ; 2021
    In:  Frontiers in Psychology Vol. 12 ( 2021-7-14)
    In: Frontiers in Psychology, Frontiers Media SA, Vol. 12 ( 2021-7-14)
    Abstract: More than 63% of Indonesian men are smokers, and smoking has long been a part of Indonesian culture and the concept of masculinity in Indonesian culture. Given the pro-smoking environment, we were interested in examining why smokers would willingly quit and whether their wives played a role in their quitting process as social factors are mentioned second most frequent as a reason for quitting smoking. Design In-depth interviews. Method We interviewed 11 couples ( N = 22)—ex-smoking husbands and non-smoking wives—in Yogyakarta, Indonesia. The data were analysed by using the thematic analysis approach. Results Four themes were discussed: (1) reasons for stopping smoking, (2) the process of quitting smoking, (3) the wives’ attitudes toward smoking, and (4) the families’ attempts to make the (ex-)smokers quit. The most commonly cited reasons for quitting were family and personal motivation. The (ex-)smokers preferred to quit without assistance and in private. The wives’ attitude toward smoking ranged from dislike to tolerance, and most did not know when their husbands were trying to quit. Both husbands and wives reported that the wives did not influence the smoking cessation process. Conclusion Indonesian ex-smokers often had multiple reasons for quitting smoking. The process was typically difficult and kept private. While wives had little influence on the cessation process, they provided support and could institute a smoking ban in the house.
    Type of Medium: Online Resource
    ISSN: 1664-1078
    Language: Unknown
    Publisher: Frontiers Media SA
    Publication Date: 2021
    detail.hit.zdb_id: 2563826-9
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  • 7
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2023
    In:  Journal of Assisted Reproduction and Genetics Vol. 40, No. 10 ( 2023-10), p. 2391-2400
    In: Journal of Assisted Reproduction and Genetics, Springer Science and Business Media LLC, Vol. 40, No. 10 ( 2023-10), p. 2391-2400
    Abstract: Reproductive health is important, but often neglected in cancer survivorship care. This study explored contraceptive use and factors associated with fertility testing among young adult survivors of childhood cancer in Germany. Methods Young adult survivors of childhood cancer were identified through the German Childhood Cancer Registry and completed a mailed survey. Survivors were queried regarding contraceptive use, reproductive goals, uncertainty about fertility, and completion or interest in fertility testing. Multivariable stepwise logistic regression models were used to calculate Odds Ratios (OR) and 95% confidence intervals (CI) as a means of identifying factors associated with completion of and interest in fertility testing. Results Survivors ( N  = 472; 57.8% female; aged 23.3 ± 1.5 years, and 14.9 ± 5.0 years from diagnosis), reported high rates of contraceptive use, including 61.2% using a single method, 30.6% dual methods, and 8.1% no/less effective methods. Few survivors had completed fertility testing (13.0%), although 58.8% were interested. Having been diagnosed during adolescence (OR = 2.66, 95%CI: 1.39–5.09), greater uncertainty about fertility (OR = 1.16, 95%CI: 1.03–1.31), and use of dual contraceptive methods (OR = 1.94, 95%CI: 1.02–3.69) were associated with having completed fertility testing. Factors associated with interest in fertility testing included goals of wanting to have children (OR = 7.76, 95%CI: 3.01–20.04) and greater uncertainty about fertility (OR = 1.19 95%CI: 1.06–1.33). Conclusion In this sample of young adults who survived childhood cancer, most reported contraceptive use. Few survivors had completed fertility testing, although more than half were interested. Interventions are needed to address potential barriers to fertility testing and help survivors manage fertility-related uncertainty.
    Type of Medium: Online Resource
    ISSN: 1058-0468 , 1573-7330
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2023
    detail.hit.zdb_id: 2016722-2
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  • 8
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2022
    In:  The Journal of Sexual Medicine Vol. 19, No. 11 ( 2022-11-01), p. 1644-1654
    In: The Journal of Sexual Medicine, Oxford University Press (OUP), Vol. 19, No. 11 ( 2022-11-01), p. 1644-1654
    Abstract: Childhood cancer and its treatment can impair survivors’ development throughout life, particularly psychosexual development, which can be affected in complex ways and is crucial for survivors’ well-being. Yet, research is scarce. Aim This study assessed psychosexual development (milestone attainment, age at attainment, perceived timing) in young adult survivors of childhood cancer. It further examined sexual satisfaction and sexual functioning, and whether survivors’ perceived timing of sexual debut was related to satisfaction or functioning. Methods A registry-based nationwide survey was completed by N = 492 German survivors of childhood cancer (age 21–26 years, 6–26 years postdiagnosis). They completed standardized measures of psychosexual milestones (eg, first kiss, sexual debut), sexual satisfaction, and sexual functioning. Psychosexual development was compared to normative data (N = 1,533). Outcomes Psychosexual development, sexual satisfaction, and sexual functioning were the primary outcome measures. Psychosexual development was characterized in three ways: milestone attainment (yes/no), age at attainment, perceived timing (“right” time, too early/late). Results Milestone attainment was comparable to normative data, except for sexual debut: Survivors were less often experienced (82.5% vs 88%; P = .002) and older at sexual debut (17.4 vs 16.2 years; g = 0.55), but most survivors (58.3%) perceived their timing as “right.” Survivors of brain tumors were least likely to have had their sexual debut, but if experienced age at sexual debut was similar to other survivors. Female survivors were somewhat more experienced than males (eg, first kiss, first relationship; & lt;10% difference), but they were somewhat older when they first kissed (g = 0.26). Age at diagnosis was unrelated to milestone attainment. Perceived early/late sexual debut was related to lower satisfaction in female survivors (P = .026), but unrelated to sexual dysfunction. Instead, partnered men reported particularly low dysfunction whereas women reported similar levels of sexual dysfunction irrespective of their relationship status (P = .049). Overall, sexual functioning was favorable (60.2%: not/barely problematic). Clinical implications Most survivors reported favorable sexual satisfaction and functioning, but a minority of survivors may need supportive services. Strengths & Limitations This project represents one of few large-scale studies on psychosexual development in childhood cancer survivors relative to normative data, and is the first to link development to sexual satisfaction/functioning. Assessing satisfaction/functioning with validated, but brief measures limits detailed insights, but was inclusive of any sexual orientation. Medical background information based on registry data was limited. Conclusion Results showed normative psychosexual development (except for sexual debut) in most survivors. A self-determined attitude toward sexuality (ie, engaging in sexual activities at the “right” time) may generally determine positive sexual experiences.
    Type of Medium: Online Resource
    ISSN: 1743-6109 , 1743-6095
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2022
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  • 9
    In: Psycho-Oncology, Wiley, Vol. 25, No. 2 ( 2016-02), p. 210-216
    Type of Medium: Online Resource
    ISSN: 1057-9249
    Language: English
    Publisher: Wiley
    Publication Date: 2016
    detail.hit.zdb_id: 1495115-0
    SSG: 5,2
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  • 10
    In: Cancer, Wiley, Vol. 123, No. 10 ( 2017-05-15), p. 1869-1876
    Abstract: The results of the current study indicate that adult survivors of childhood cancer do not differ from healthy controls with regard to their psychosexual development, sexual satisfaction, and relationship status satisfaction. However, more intense neurotoxic treatment appears to be associated with a higher risk of psychosexual impairment, and may be a more meaningful risk indicator than diagnostic category alone.
    Type of Medium: Online Resource
    ISSN: 0008-543X , 1097-0142
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2017
    detail.hit.zdb_id: 1479932-7
    detail.hit.zdb_id: 2599218-1
    detail.hit.zdb_id: 2594979-2
    detail.hit.zdb_id: 1429-1
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