The level of brutality and violence against children abducted and forcefully conscripted by the Lord's Resistance Army (LRA) in northern Uganda pricked the conscience of humanity. The suffering of the people in northern Uganda was described by Jan Egeland, the former United Nations Under-Secretary for Humanitarian Affairs, as 'the biggest forgotten humanitarian crisis in the world'. This study is primarily concerned with the plight of child soldiers in northern Uganda and how their effective reintegration and rehabilitation (RR) could lead to successful peacebuilding. The study is premised on the hypothesis that 'the promotion of the RR of former child soldiers by providing psychosocial support based on traditional and indigenous resources may contribute to conditions of peace and stability in northern Uganda'. The main contribution of this research is that it explores the relevance of psychosocial support based on the traditional and indigenous resources to the RR of child soldiers and peacebuilding of war-torn societies. Psychosocial support based on traditional and indigenous resources as an element of peacebuilding has been the neglected element of peacebuilding by the liberal peacebuilding interventions in most war-torn societies. For example, while traditional and indigenous resources in northern Uganda have been instrumental in the RR of former child soldiers, most scholars and policy makers have largely paid attention to the usual official government and United Nations structured top-down interventions that emphasize Western approaches of peacebuilding. More so, the official approaches have tended to marginalize the plight of former child soldiers in the reconstruction and peacebuilding of northern Uganda. Yet, failing to pay sufficient attention to effective RR of child soldiers could undermine the peace dividends already achieved in northern Uganda. The study also analyses the limitations of psychosocial support based on traditional and indigenous resources in the RR of former child soldiers. It further examines why Western approaches of psychosocial support in the RR of child soldiers have remained in use in spite of the criticisms levelled against them. The study examines other peacebuilding interventions, both official and unofficial, that have been implemented in northern Uganda. In terms of key findings, the study establishes that traditional and indigenous resources are still popular and have been widely used in northern Uganda in the RR of child soldiers. Majority of former child soldiers who were interviewed observed that they found traditional and indigenous resources more helpful than the Western models of psychosocial support. However, it was also established that there is a significant section of former child soldiers who found Western models more relevant in their RR processes. Based on these findings, the study recommends an integrative and holistic model of psychosocial support that blends good elements from both traditional and indigenous resources and Western approaches with greater emphasis on the former.

Bakgrund: Personal inom hälso- och sjukvården ska “beakta ett barns behov av information, råd och stöd” när ett barns förälder eller annan vuxen i barnets närhet lider av eller drabbas av sjukdom, skada, beroende eller vid dödsfall. Barn i familjer där minst en förälder har ett missbruk eller beroende löper större risk att utsättas för fysiskt och psykiskt våld. Barn som växer upp under sådana förhållanden löper även en ökad risk att själva utveckla beroendeproblematik. Information och stöd kan vara avgörande för deras framtida hälsa. Syfte: Att undersöka vilken kunskap och vilka erfarenheter sjuksköterskor verksamma inom beroendepsykiatrin har av att uppmärksamma om det finns barn i patientens närhet som är i behov av information och stöd, samt vilka hindrande respektive främjande faktorer som finns för att kunna tillgodose detta behov. Metod: Sex sjuksköterskor deltog i individuella intervjuer. Intervjuerna analyserades med manifest innehållsanalys. Resultat: Samtliga respondenter uppgav att de alltid tillfrågar sina patienter om det finns barn i deras närhet. De främjande faktorer som har framkommit är att det hos sjuksköterskorna fanns en vilja till förbättring och utveckling i verksamheten samt att barnen uppmärksammas. De hindrande faktorerna beskrivs vara miljön inom beroendepsykiatrin, sjuksköterskornas utbildningsläge, olika rädslor samt viss tidsbrist. Slutsats: Om en strukturerad handlingsplan för att stödja och informera barnen fanns att tillgå skulle detta tillsammans med det engagemang som redan finns hos sjuksköterskorna kunna leda till ett förbättrat stöd till de barn som lever tillsammans med en vuxen med missbruksproblematik. / Background: Staff within the Swedish health care should “consider a child’s need of information, advice and support when the child’s parent or other adult in the child’s vicinity suffers from illness, injury, addiction or death”. Children in families where one parent suffers from substance addiction or abuse are at greater risk of being exposed to physical and psychological violence. Children who grow up under those circumstances are also at greater risk of developing addiction problems. Information and support may be vital for their future quality of life. Aim: To examine the knowledge and experiences nurses working in the field of addicition psychiatry have regarding inquiring about whether there are children close to their patient who are in need of information, support, and also what impeding and promoting factors they experience in regards to providing that information and support to the child. Methods: Six nurses participated in individual interviews. The interview results was analyzed using a manifest content analysis. Results: All of the nurses said that they always ask their patients if they have children among them. The promoting factors are their will to improve and development of the business and that they pay attention to the children. The impeding factors are described as the environment within the psychiatry, the nurses education, different fears and a lack of time. Conclusions: If a structured plan to support and inform the children were available, together with the commitment the nurses have expressed, could lead to an improved support for children living with an adult with substance abuse problems.

Hjärtsvikt är en av Sveriges största folksjukdomar och en vanlig orsak till sjukhusvistelse. Kvalificerad professionell vård i hemmet kan minska antalet inneliggande vårddygn för den hjärtsviktssjuke. Lyfts inte hjärtsviktssjuka personers behov av stödjande insatser fram finns risk för att professionella vårdare i hemmet inte uppmärksammar den sjukes behov av psykosocialt stöd. Syftet med litteraturstudien var att beskriva behovet av psykosocialt stöd för den hjärtsviktssjuke personen som vårdas i hemmet. Systematisk litteraturstudie valdes där 19 artiklar analyserades genom kvalitativ innehållsanalys. Det framkom två huvudkategorier; professionella stödet och det informella stödet. Resultatet beskriver behovet av stödjande insatser i form av psykosocialt stöd den hjärtsviktssjuke erfar i hemmet. Då den professionella vården gjorde en helhetsbedömning av den hjärtsviktssjuke uppmärksammades psykosociala behov hos den sjuke. Genom att stärka den inneboende förmågan med stödjande insatser kunde den sjuke hantera de psykiska symtom som hjärtsvikt medförde. För det professionella stödet var delaktighet av största vikt, delaktighet ökade känslan av att bemästra sjukdomssituationen och stärkte värdigheten hos den sjuke. Litterturstudien riktar sig främst till distriktsköterskor i kommunal hemsjukvård och är överförbar på personer med andra palliativa sjukdomar. Vidare forskning för att få en helhetsbild av den hjärtsviktssjukes vård i hemmet skulle vara att undersöka hur atienternas copingförmåga påverkar deras psykosociala välbefinnande. / Heart failure is one of the most common diseases and a major cause of hospitalization in Sweden. Professional health care provided at home might decrease the number of days of hospitalization for the heart failure patient. If not the heart failure patient´s need for support takes into consideration, there is a risk that professional caregivers in the home do not pay attention to the patient`s need of psychosocial support. The purpose of this study was to describe the heart failure patient's need for psychosocial support while being cared for in the home. A systematic literature review was chosen, 19 articles where selected and analyzed by qualitative content analysis. Two main categories revealed: professional support and informal support. Results of the study describe the supportive services in the form of psychosocial support on heart failure patient experience in the home. The professional care made a holistic assessment of the patient and they noticed psycho-social needs. By enhancing the inherent ability with supportive services, the patient could cope with the mental symptoms of heart failure. For the professional support the involvement of the supporting effort was of paramount importance. If the heart failure patient felt participating in the care, the patients feeling of mastering the disease situation and strengthening of the dignity increased. The literature study caters mainly to district nurses in municipal home care and is transferable to persons with other palliative diseases. Further research is needed to gain an overall picture of the heart failure patient's home care would be to examine how patients' coping, affect their psychosocial well-being.

This practicum project is an investigation of the importance of providing a supportive and restorative temporary accommodation facility for breast cancer patients who are traveling from rural areas of Manitoba to receive treatment in Winnipeg. Exploring key areas of restorative and healing design in the literature review allowed for a comprehensive analysis and examination into three main areas. The key themes of restorative design are; Biophilic Design, Theory of Supportive Design, and supportive domestic environments. It is through this exploration of restorative design that a design for the Centre will be proposed.

Breast cancer is a common disease in Australia and exerts a sizable burden to individuals, families, and health care resources. Studies that assess healthrelated quality-of-life (HRQoL) are particularly relevant as survivors must learn to live with breast cancer, undergo prolonged treatment, use new pharmacological agents, monitor and adjust to a serious condition. Relatively little published evidence exists on the effects of rehabilitation programs for breast cancer survivors but those published demonstrate positive health benefits that alleviate both physical and psychological problems. This study aimed to partly fill this gap and had the objectives of: a) estimating the effectiveness of two rehabilitation interventions for breast cancer survivors over time compared to a non-intervention comparison group; and b) ascertaining which option was cost-effective when taking a societal perspective. Effectiveness was described in terms of HRQoL and functional status and there was a particular focus on upperbody morbidity since the two interventions primarily addressed this aspect of rehabilitation. The study participants comprised three groups: one group received a physiotherapy home-visits service (DAART), the second attended a gentleexercise group program (STRETCH), while the third represented a nonintervention comparison group for later analyses only. Data collection was primarily by way of postal questionnaires while medical and cost data abstraction was also necessary. Reliable and validated instruments were used to collect HRQoL and utility data. The Functional Assessment of Cancer Therapy - Breast Cancer plus the Arm Morbidity module (FACT-B+4), Disabilities of the Arm, Shoulder and Hand (DASH), and the Subjective Health Estimation (SHE) instruments were chosen for their high psychometric performance with various populations, their brevity, quick administration and relevance to a breast cancer sample. Missing data was a small concern overall, however, baseline differences were present and mixed across the three participant groups indicating selection bias was present. DAART showed poorer demographic indicators of socioeconomic status and were older, STRETCH participants had poorer disease and treatment profile, while the non-intervention women had poorer general health characteristics. Based on bivariate analyses, age, presence of comorbidities, chemotherapy, high blood pressure, work status (unpaid/paid), hormone therapy were determined to be factors requiring control for in the multivariate analyses. Benefits were found for multiple dimensions of HRQoL for the DAART intervention. On average, HRQoL levels were fairly high across the three alternative participant groups and no significant group differences were found. However, approximately one-third of the women experienced declining HRQoL between 6- to 12-months and their scores were significantly poorer than other participants. STRETCH incurred higher overall costs per participant (on average) than DAART and the non-intervention groups. This was driven by higher leisure time forgone, travel and higher community costs. DAART experienced the highest program costs (or health system costs). Therefore, by taking a societal perspective, and incorporating the estimated value of more intangible or indirect costs (e.g., volunteers, travel costs etc.) the STRETCH program was more costly. The greatest influence on higher costs incurred by the STRETCH participants was the average out-of-pocket expenses for health care services purchased during the previous 12 months for breast cancer-related problems. Although an exploratory finding, the DAART group emerged as the cost-effective option, that is, the incremental cost per QALY gained was $1,344 compared to STRETCH $14,478. The key drivers in the cost-effectiveness modelling were utility values and health service expenditure. When uncertainty was quantified by way of Monte Carlo modelling, DAART remained the cost-effective choice. This project has highlighted that while many women seem to breeze through their breast cancer diagnosis and treatment, there are a substantial number of women who do not. Therefore, it is quite mistaken to generalise the favourable levels of HRQoL and expect that all women will get back to 'normal'. Given that HRQoL is a very complex concept, it was important to use validated tools that had undergone extensive testing with sound psychometric properties. Health care activities observed in their natural 'real world' setting are preferable to minimise biases that may cause more favourable results than truly occur and allow a better assessment on the impact of the service. The project findings have been interpreted while respecting a number of limitations. These have included potential selection and response bias, missing data, and small numbers of intervention women and defined socio-demographic profiles. Taken together, these are likely to overestimate the true outcomes. Arguably, selection bias and the timing of the interventions are likely to be the strongest factors affecting the generalisability of these findings. Given the caveats of this research, the following recommendations were made: 1. Greater awareness and/or screening of adjustment problems among survivors needs to be considered during recovery from breast cancer surgery. 2. Early physiotherapy should be given to all breast cancer survivors after surgery due to the potential functional, physical and overall HRQoL benefits that may arise. 3. Professionally-led group exercise therapy with psychosocial care appears to have a neutral effect on upper-body recovery and improving HRQoL. However, it provides advantages for attendees in the form of peersupport, education, a holistic focus and the potential for addressing previously unrecognised psychological problems in a caring and acceptable environment. This program, with large community resources (provided voluntarily), represents a very low-cost outlay for health services and should be given support and consideration during follow-up care after breast surgery. 4. From a societal perspective, a home-visiting physiotherapy service represents a cost-effective means to provide rehabilitative care for breast cancer patients and represents an excellent public health investment. Several topics for further research are likely to be important in the future including, among others, other modes and settings of rehabilitation service delivery, barriers to psychosocial care and the indirect financial and work consequences of having breast cancer.

Mentoring has been found to be an effective psychosocial buffer to occupational stress (Chao & Walz, 1992; Noe, 1988; Siege1 & Reinstein, 2001). Mentoring provides support for personal confirmation, acceptance, friendship and role modelling (Kram 1985, 1986) The current study was part of an initiative within the New Zealand Police to introduce mentoring as part of a supported induction for new Police Constables into the organisation. The aim was to evaluate the use of mentoring as a psychosocial support in this induction process. Using a Solomon Four Group design the 254 subjects (180 protégé(e)s and 74 mentors) were randomly assigned to four groups. These groups were (i) those who had a pre-test, assigned a mentor and post test (ii) those who had a pre-test and post test (iii) those who had a mentor and a post test (iv) those who had a post test only. Testing included two questionnaires; a Combined Measures Questionnaire – which incorporated six psychometric tests including BDI, BHS, MHI, CMTS, HSCL-21 and ITQ; and a Mentor Relationship Questionnaire. The former was administered at pre- and post- test in accordance with the experimental design while the later [i.e. latter] was only administered at the end of the mentoring programme. There was no clinically significant effect noted in terms of change in psychological well-being or distress for either protégé(e)s or mentors (p > .05). There was a significant effect of mentoring in terms of an increase in intent to quit, F(1,10) = 7.43, p = .02 and a trend toward significance for decreased general distress levels F(1,10) = 4.80, p = .53 for the mentors at the end of the experimental period. These findings are tempered by a small control group (n=2). The main finding of this study was that positive outcomes were reported about the mentor relationship, on the Mentoring Relationship Questionnaire, from both protégé(e)s and mentors. These results were achieved in less than three sessions. From these findings it may be concluded that there is a place for a formal mentoring programme in the induction process of the New Zealand Police organisation.

Background: In Sweden, approximately 800 young adults between 16-30 years of age are affected by a cancer disease. Studies has shown that this is not only the medical treatment that affects how patients live with their cancer, but also how their psychological health are affected. When a young adult gets a cancer diagnosis can thoughts about the disease, death, changed body image, loss of fertility etcetera be particularly disturbing and anxiety evoking. To achieve good health and quality of life, care and good relations between patient and nurses are important. Aim: The aim of the literature study was to: 1) Examine young adults experiences of a cancer disease, 2) Experienced need of support from healthcare professionals and 3) Experiences of psychosocial support from nurses during and after treatment. Method: A literature study where qualitative articles were searched through the database Pubmed. 10 original articles out of a total of 27 articles were included because they met the inclusion criteria and were either medium or high quality. Results: The analysis revealed nine themes based on the three questions; attitudes and emotional reactions related to the disease, changed perception of identity, positive aspects of the disease, post-treatment reactions, support from family and friends, support and adaptation within health care, informative support, personal and emotional support and participation and trust. The need for information from healthcare professionals was particularly prominent, especially on the topics of sexuality and fertility. The importance of obtaining information in a manner that is easy to understand was highlighted. The majority of young adults experienced positive support from nurses which made them gain confidence, trust and joy. Conclusion: Young adults have an increased need for continuous information and guidance during and after treatment. Nurses need to be better at communicating, which would contribute to increased understanding and provide security for the patient in order to feel better mentally. Nurses have an important role in providing advice and information in areas which the patient lack knowledge in.

Abstract The purpose of this study was to develop a hypothetical model of genetic counseling for male hereditary breast cancer mutation (BRCA1/2) carriers. The methodological approach involved mixed methods. The aim of the first phase was to describe male BRCA1/2 mutation carriers’ genetic counseling, experiences and needs for developing genetic counseling. Quantitative data were acquired using a patient counseling questionnaire (n=35) based on consecutive sampling, whereas theme-based interviews (n=31) were conducted as a qualitative approach. In the second phase, the theme-based interview data were used to describe males’ experiences after identification as BRCA1/2 mutation carriers and effects of identification as a carrier on their lives (n=31). The data were analyzed using descriptive statistics and inductive content analysis. The results of the study were combined into a model describing genetic counseling for male BRCA1/2 mutation carriers. Based on the quantitative data, the genetic counseling was evaluated as good. Psychosocial support was insufficient. According to the qualitative data, there was lack of noticing individual wishes and needs during the genetic counseling process. Operational conditions of departments of clinical genetics and genetic healthcare professionals’ readiness to provide gentic counseling were varied. Identification as a BRCA1/2 mutation carrier caused varied emotional reactions associated with identification as a carrier, hereditary transmission of the mutation, cancer risks and possibility of developing cancer. However, the duration of the reactions varied. Identification as a carrier had effects on male carriers’ health and social wellbeing. According to the hypothetical model, genetic counseling was based on the backgrounds and individual needs of the male BRCA1/2 mutation carriers, which was implemented with appropriate operational conditions. It included sufficient psychological support, which genetics healthcare professionals had professional responsibility for implementing. The information study provided can be used to broaden the knowledge base of nursing science in clinical genetics. The information may also be utilized in continued nursing education. / Tiivistelmä Tutkimuksen tarkoituksena oli kehittää periytyvän rintasyöpäalttiusmutaation (BRCA1/2) kantajamiesten hypoteettinen perinnöllisyysneuvontamalli. Tutkimuksessa käytettiin monimenetelmämetodologiaa. Ensimmäisessä vaiheessa kuvattiin BRCA1/2-alttiusmutaation kantajamiesten perinnöllisyysneuvontaa, perinnöllisyysneuvontakokemuksia ja kehittämistarpeita. Aineisto kerättiin kokonaisotannalla kvantitatiivisesti Potilasohjaus-kyselylomakkeella (n=35) ja kvalitatiivisesti teemahaastatteluilla (n=31). Toisessa vaiheessa kuvattiin ensimmäisessä vaiheessa kerätyllä haastatteluaineistolla kantajamiesten kokemuksia alttiusmutaation kantajuudesta ja kantajuuden vaikutuksista elämään (n=31). Tutkimuksen aineistot analysoitiin tilastollisin menetelmin ja induktiivisella sisällönanalyysillä. Tutkimuksen tulosten perusteella muodostettiin BRCA1/2-alttiusmutaation kantajamiesten perinnöllisyysneuvontamalli. Kvantitatiivisen tutkimuksen perusteella perinnöllisyysneuvonta arvioitiin hyväksi. Psykososiaalisen tuen saaminen oli vähäistä. Kvalitatiivisen tutkimuksen mukaan kantajamiesten yksilöllisten toiveiden ja tarpeiden huomioiminen perinnöllisyysneuvontaprosessin aikana oli puutteellista. Kliinisen genetiikan yksiköiden toimintaedellytyksissä ja perinnöllisyysneuvonnan antajien ohjausvalmiuksissa oli vaihtelevuutta. BRCA1/2-alttiusmutaation kantajuus aiheutti kantajamiehille eriasteisia ja -kestoisia emotionaalisia tunteita, jotka liittyivät kantajuuteen, alttiusmutaation periytymiseen, syöpäriskiin ja syöpään sairastumiseen. Kantajuudella oli lisäksi vaikutusta kantajamiesten terveydelliseen ja sosiaaliseen hyvinvointiin. Periytyvän rintasyöpäalttiusgeenin hypoteettisen mallin perusteella perinnöllisyysneuvonta oli BRCA1/2-alttiusmutaation kantajamiehen taustatilanteeseen ja yksilölliseen tarpeeseen perustuva neuvonta, joka oli toteutettu asianmukaisin toimintaedellytyksin. Se sisälsi riittävästi psykososiaalista tukea ja sen antajalla oli ammatillinen vastuu perinnöllisyysneuvonnan toteuttamisesta. Tutkimuksessa tuotetun tiedon avulla lisätään hoitotieteellistä tietoperustaa perinnöllisyyslääketieteen alueelle. Tietoa voidaan hyödyntää myös hoitotyön täydennyskoulutuksessa.

Disaster survivors, facing many aspects of mental distress, sometimes are forced to stay in temporary housing for years. Their psychosocial needs have changed after the traumatic event, but existing temporary housing designs do not respond to their real needs, nor acknowledge the capacity within the community as a whole.  This thesis aims to answer the question of how post-disaster temporary housing contributes to psychosocial aspects of community resilience building.  Based on the literature review of existing studies on post-disaster temporary housing, discussions on key factors of community psychosocial resilience and the psychosocial impact of temporary housing were conducted in this thesis. These discussions were followed by a comparative case study on the implementation and follow-up actions of two post-disaster temporary housing projects in China and Japan.  The analysis of these two topics and the case study reveal gaps between humanitarians and architects, when they work together to develop temporary housing, as well as aspects that can be improved for temporary housing to better meet the needs of its inhabitants and empower them for improved recovery.  The results indicate that temporary housing has a psychosocial impact on its inhabitants. By designing the built environment of temporary housing that strengthens shared community identity and promotes mutual help from community members, community resilience can be better fostered. Achieving this will require better coordination between humanitarians and architects, as well as the involvement of other interdisciplinary professionals.

Bakgrund: Tonåringar och unga vuxna (15–39 år) som insjuknar i cancer möts av emotionella, fysiska och sociala utmaningar. Utöver rädsla för cancersjukdomen kan utbildning och jobb samt den ekonomiska situationen oroa. Forskning visar att tonåringar och unga vuxna med cancersjukdom har högre förekomst och större risk för psykosociala besvär än personer utan cancer i samma ålder och äldre patienter med cancersjukdom. Syfte: Att sammanställa litteratur om de psykosociala behov som tonåringar och unga vuxna med cancer har. Metod: En allmän litteraturstudie genomfördes med fokus på kvalitativa studier och studier med mixad metod. Femton artiklar kvalitetsgranskades och analyserades med innehållsanalys. Resultat: Innehållsanalysen resulterade i fyra kategorier med tillhörande subkategorier: Önskan att upprätthålla ett vanligt liv, Utmanande känslor och tankar, Socialt stöd och Oro för framtiden. Ett flertal psykosociala behov och utmaningar beskrevs vilka omfattade social isolering, fertilitetsoro, oro för jobb/utbildning och ekonomisk situation. I de analyserade artiklarna beskrevs ett behov av att få ha en vanlig vardag och bli behandlad som tidigare, men att de återigen blivit beroende av sina föräldrar. Det psykosociala stödet från familj, partner, vänner och hälso- och sjukvården beskrevs variera i omfattning och utförande. I flera av studierna beskrevs en önskan av att träffa andra i samma situation, att man kände sig malplacerad i cancervården och önskade mer åldersanpassad information. Slutsats: Tonåringar och unga vuxna är en speciell patientgrupp som skiljer sig från de typiska cancerpatienterna. I denna litteraturöversikt omfattande 15 kvalitativa studier framkommer otillfredsställda psykosociala behov hos unga personer med cancer. För att bättre möta den här gruppens psykosociala behov skulle ett arbetssätt utifrån den modell House beskriver kunna utformas, det vill säga genom att ta hänsyn till deras behov av emotionellt, bekräftande, informativt och instrumentellt stöd. / Background: Adolescents and young adults (15–39 years) who develop cancer face emotional, physical and social challenges. In addition to fear of the cancer disease, education and work as well as the financial situation can cause concern. Research shows that adolescents and young adults with cancer have a higher incidence and greater risk of psychosocial problems than people without cancer of the same age and older patients with cancer. Aim: To compile literature on the psychosocial needs of adolescents and young adults with cancer. Method: A general literature study was conducted with a focus on qualitative studies and mixed method studies. Fifteen articles were quality reviewed and analyzed using content analysis. Results: The content analysis resulted in four categories with associated subcategories: The desire to maintain an ordinary life, Challenging feelings and thoughts, Social support and Worry about the future. A number of psychosocial needs and challenges were described, which included social isolation, fertility concerns, concerns about work/education and financial situation. In the analyzed articles, a need to have a normal everyday life and to be treated as before was described, but that they once again became dependent on their parents. The psychosocial support from family, partner, friends and health care was described as varying in scope and execution. In several of the studies, a desire to meet others in the same situation was described, that they felt out of place in cancer care and wanted more age-appropriate information. Conclusion: Adolescents and young adults are a special patient group that differs from the typical cancer patients. In this literature review comprising 15 qualitative studies, unsatisfied psychosocial needs of young people with cancer emerge. In order to better meet the psychosocial needs of this group, a working method based on the model described by House could be designed, that is, by taking into account their need for emotional, affirmative, informative and instrumental support.