Anna Ivanova

• Ivanova, Anna; Amdal, Cecilie Delphin; Kvalem, Ingela Lundin & Reme, Silje Endresen (2026). Multidomain predictors of long-term work disability in late survivorship after head and neck cancer. Supportive Care in Cancer. ISSN 0941-4355. 34(3). doi: 10.1007/s00520-026-10524-1. Fulltekst i vitenarkiv Vis sammendrag

  Abstract Purpose To estimate the prevalence of long-term work disability (LTD) among head and neck cancer (HNC) survivors more than five years posttreatment, compare profiles of employed, retired, and LTD groups, and identify independent predictors of LTD versus employment. Methods Late effects were assessed using the EORTC QLQ-C30, EORTC QLQ-H&N35, Chalder Fatigue Questionnaire, and Body Image Scale in a cross-sectional sample of 251 HNC survivors (mean 8.3 years posttreatment). Employment status was categorized as employed, retired, or LTD (> 12 months sick leave). Predictors of LTD were examined among working-age survivors (n = 145) using hierarchical logistic regression. Results LTD prevalence was 19% overall and 33% among working-age survivors. In multivariable models, better physical functioning (OR = 0.13, 95% CI 0.05–0.34) and better cognitive functioning (OR = 0.41, 95% CI 0.18–0.93) were associated with lower odds of LTD, while blue-collar occupation (OR = 6.70, 95% CI 1.18–38.05) and body image distress (OR = 13.34, 95% CI 1.25–142.07) were associated with higher odds. Treatment modality of chemoradiotherapy plus surgery vs radiotherapy was marginally associated with lower LTD odds (OR = 0.06, 95% CI 0.01–0.87), but this finding should be interpreted cautiously due to the small RT subgroup. Conclusions More than five years posttreatment, LTD remains common and is best explained by current physical and cognitive functioning, body image distress, and occupational context rather than historical clinical exposures or any single symptom.

• Ivanova, Anna; Fluit, Sam; Fischer, Nantje; Soest, Tilmann Martin von & Kozák, Michal (2025). Masturbation Trajectories from Late Adolescence into Mid-Adulthood: A Population-Based Longitudinal Study. Journal of Sex Research. ISSN 0022-4499. doi: 10.1080/00224499.2025.2489091. Fulltekst i vitenarkiv
• Kvalem, Ingela Lundin; Nygaard, Ida Maria Dahr; Træen, Bente; Ivanova, Anna & Dahlgren, Anna Maria Camilla Lindvall (2024). Menstrual attitudes in adult women: A cross-sectional study on the association with menstruation factors, contraceptive use, genital self-image, and sexual openness. Women's Health. ISSN 1745-5057. 20, s. 1–14. doi: 10.1177/17455057241249553. Fulltekst i vitenarkiv
• Ivanova, Anna; Cano, Ruben Rodriguez; Kvalem, Ingela Lundin; Harcourt, Diana; Kiserud, Cecilie E. & Amdal, Bente Cecilie Delphin (2022). Body image concerns in long-term head and neck cancer survivors: prevalence and role of clinical factors and patient-reported late effects. Journal of cancer survivorship. ISSN 1932-2259. 17, s. 526–534. doi: 10.1007/s11764-022-01311-y. Fulltekst i vitenarkiv Vis sammendrag

  Purpose Head and neck cancer (HNC) patients are at risk of long-term body image distress (BID). We aimed to investigate the severity of BID in long-term HNC survivors and to explore the associations between sociodemographic and clinical factors, patient-reported late effects, and cancer-related body image (BI) concerns. Methods This cross-sectional study included quality of life and BI assessment in an 8-year (SD = 1.58) follow-up after treatment among 258 HNC survivors. Multinomial logistic regression analysis was used to investigate the relationship between three groups of BI concerns (no concerns, mild to moderate concerns, and BID) and patient-reported late effects. Sociodemographic and clinical variables were included in the model as covariates. Results A total of 51.2% of participants had mild to moderate BI concerns, and 9.5% reported BID. Compared to those with no BI concerns, participants with BID were more likely to live without a partner, to have had radiotherapy and surgery, and to report worse emotional functioning and higher oral and throat pain. Compared to participants with no BI concerns, those with mild to moderate concerns reported higher oral and throat pain and speech problems. Conclusions Some level of cancer-related BI concerns persisted in the majority of HNC survivors many years after treatment, while a small proportion of survivors experienced BID. BI concerns were associated with treatment modality and patients’ daily functioning and symptoms. Implications for Cancer Survivors Insight into factors associated with BI problems may help to identify survivors at risk and may facilitate closer follow-up of survivors in need.

• Ivanova, Anna & Kvalem, Ingela Lundin (2021). Psychological predictors of intention and avoidance of attending organized mammography screening in Norway: applying the Extended Parallel Process Model. BMC Women's Health. 21. doi: 10.1186/s12905-021-01201-y. Fulltekst i vitenarkiv Vis sammendrag

  Background Mammography screening is the main method for early detection of breast cancer in Norway. Few studies have focused on psychological determinants of both attendance and non-attendance of publicly available mammography screening programs. The aim of the current study, guided by the Extended Parallel Process Model, was to examine how psychological factors influence defensive avoidance of breast cancer screening and intention to attend mammography. Methods Cross-sectional survey data from a community sample of women living in Norway aged ≥ 18 (N = 270), and without a history of breast cancer, was collected from September 2018 to June 2019 and used to investigate the relationships between the Extended Parallel Process Model (EPPM) constructs and two outcomes: defensive avoidance of breast cancer screening and intention to attend mammography within the next two years. After adjusting for confounding factors, the hierarchical multiple linear regression analyses was conducted to assess the ability of the independent variables based on the EPPM to predict the two outcome variables. Significance level was chosen at p < 0.05. Results Multivariate analyses showed that defensive avoidance of breast cancer screening was predicted by lower perceived susceptibility to breast cancer (β =  − 0.22, p = 0.001), lower response efficacy of mammography screening (β =  − 0.33, p = 0.001), higher breast cancer fear (β = 0.15, p = 0.014), and checking breasts for lumps (β =  − 0.23, p = 0.001). Intention to attend mammography within the next two years was predicted by higher response efficacy of mammography screening (β = 0.13, p = 0.032), having a lower educational level (β =  − 0.10, p = 0.041), and regular previous mammography attendance compared to never attending (β = 0.49, p = 0.001). Conclusions The study revealed that defensive avoidance of breast cancer screening and intention to attend mammography were not predicted by the same pattern of psychological factors. Our findings suggest future health promotion campaigns need to focus not only on the psychological factors that encourage women’s decision to attend the screening, but also to counter factors that contribute to women’s decision to avoid it.

Se alle arbeider i NVA

• Garbo, Gro Lien & Ivanova, Anna (2026). Friskmeldt fra kreft, men med langtidsplager som burde vært fulgt opp. [Internet]. Forskning.no. Fulltekst i vitenarkiv Vis sammendrag

  Ny studie viser behov for tettere oppfølging også på lengre sikt.

• Ivanova, Anna & Ystrom, Eivind (2026). Temporal relationships between dysmenorrhea and depression in Norwegian women. Fulltekst i vitenarkiv
• Ystrom, Eivind & Ivanova, Anna (2026). Do reproductive factors shape depression stability? Early menarche, endometriosis and PMS in longitudinal registry data. doi: https:/2026.ehps.net/wp-content/uploads/2026/08/ehps26_final_program_27_08-1.pdf. Fulltekst i vitenarkiv Vis sammendrag

  Background: Menstrual and gynaecological conditions may increase depression risk, but it is unclear whether they relate to onset versus persistence. Methods: 85,637 women aged 14 to 72 from the Norwegian Mother, Father and Child Cohort Study (MoBa) contributed with 18,415,809 person-months of patient registry data (2006–2023) on primary-care depression diagnosis. Early menarche (before age 12), endometriosis, and Premenstrual Syndrome (PMS) was recorded by questionnaire. Log-binomial regression was used to estimate risk ratios (RR) for population average effects and conditioned on prior-month depression to additionally test condition*prior-depression (stability) interactions and condition*age interactions. Results: Depression was prevalent in 26.3% of women across the 18-year observation period and incident within 1.18% of the person-months. Early menarche, endometriosis, and PMS predicted higher depression risk RR=1.22 (95%CI 1.15-1.29), 1.19 (95%CI 1.04-1.36), and 1.68 (95%CI 1.61-1.75). Conditioning on prior month depression status, main effects were for early menarche RR=1.21 (95%CI 1.15-1.28), endometriosis RR=1.19 (95%CI 1.04-1.35), and PMS remained RR=1.70 (95%CI 1.63-1.77); indicating associations were primarily with transitions into depression rather than persistence. Early menarche RR=0.83 (95%CI 0.79-0.88), endometriosis RR=0.83 (95%CI 0.72-0.95), and PMS RR=0.59 (95%CI 0.56-0.61) all contributed to lower stability of depression. Furthermore, early menarche gave a diminishing risk for depression with older age. Conclusions: Early menarche, endometriosis, and PMS mark elevated depression burden. However, this appears to happen primarily through increased transitions into depression rather than chronicity. Hence, early age of menarche, endometriosis, and PMS may help identify women eligible for preventive mental health interventions rather than being fixed markers of life-course depression risk.

• Haugan, Adrian Møller & Ivanova, Anna (2026). Ny trend: Alvorlige tall om ereksjonsproblemer. [Internet]. Nettavisen. Fulltekst i vitenarkiv Vis sammendrag

  Mange tror den mannlige seksualiteten alltid fungerer. For svært mange menn – også unge – er det ikke slik.

• Ivanova, Anna; Evje, Jacob & Garbo, Gro Lien (2026). Helt tilfeldig hva terapeuter kan om LHBT+-personer - Forskningsnytt. [Internet]. Forskningsnytt, UiO. Fulltekst i vitenarkiv Vis sammendrag

  Mange skeive opplever å bli oversett, misforstått eller å måtte lære opp sin egen behandler når de oppsøker psykisk helsevern. Det framgår av to nye rapporter, som beskriver stor kunnskapsmangel.

• Ivanova, Anna & Skjeldal, Eskil (2026). Hva vet vi om psykisk helsearbeideres erfaringer i møte med skeive pasienter? - Erfaringskompetanse.no. [Internet]. Erfaringskompetanse.no. Fulltekst i vitenarkiv Vis sammendrag

  Anna Ivanova (PhD-kandidat, psykologisk institutt, UiO) forteller her om rapporten som sammenstiller forskningsbasert kunnskap om psykisk helsearbeideres erfaringer i møte med skeive pasienter. Rapporten bidrar med et rammeverk som kan brukes for å bedre forstå hvordan barrierer og tilretteleggere oppstår på individ-, organisasjons- og strukturnivå.

• Evje, Jacob & Ivanova, Anna (2026). Skeive i møte med psykiske helsetjenester: Barrierer, tillitsbrudd og kunnskapsbehov. Fulltekst i vitenarkiv
• Ivanova, Anna (2025). Skeives psykiske helse fra tjenesteyteres perspektiv - Funn fra rapport 2. Fulltekst i vitenarkiv
• Evje, Jacob; Ivanova, Anna; Nysæter, Maren Kristin; Fischer, Nantje & Øvrum, Marthe Holmedal (2025). Skeives helse-søkende atferd - Funn fra rapport 1. Fulltekst i vitenarkiv
• Ivanova, Anna & Kvalem, Ingela Lundin (2025). The Psychological Dimensions of Menstrual Pain: Exploring Attitudes, Emotions, and Pain Intensity. Fulltekst i vitenarkiv
• Ivanova, Anna & Kvalem, Ingela Lundin (2025). Menstrual Pain in Norwegian Women: The Role of Perimenstrual Symptoms, Sexual Activity and Sociodemographic Factors. Fulltekst i vitenarkiv
• Ivanova, Anna; Amdal, Bente Cecilie Delphin & Kvalem, Ingela Lundin (2024). Sexual Interest and Enjoyment in Partnered Long-Term Head and Neck Cancer Survivors: The Role of Symptoms and Subjective Health. Fulltekst i vitenarkiv
• Ivanova, Anna; Amdal, Bente Cecilie Delphin & Kvalem, Ingela Lundin (2024). The Role of Body Image Distress and Visible Differences in Social Functioning among Long-term Head and Neck Cancer Survivors. Fulltekst i vitenarkiv
• Evje, Jacob; Nysæter, Maren Kristin; Nygård, Stine; Ivanova, Anna; Bjaalid, Emily & Fluit, Sam [Vis alle 9 forfattere av denne artikkelen] (2024). LGBTQ+ health-seeking: A scoping review of health care needs, experiences and barriers. Fulltekst i vitenarkiv
• Ivanova, Anna & Nygård, Stine (2024). Validating a Gender-Neutral Version of Female Genital Self-Image Scale in the Norwegian Population: Preliminary findings from a Pilot Study. Fulltekst i vitenarkiv
• Ivanova, Anna; Amdal, Bente Cecilie Delphin & Kvalem, Ingela Lundin (2024). Psychological barriers to Work Integration in Head and Neck Cancer (HNC) Survivors: The Role of Negative Emotions and Body Image in Long-Term Work Disability. Fulltekst i vitenarkiv
• Ivanova, Anna & Tønnessen, Maria Schiller (2024). Får meldinger fra sinte menn hun aldri har møtt. [Internet]. TV2.no. Fulltekst i vitenarkiv
• Ivanova, Anna; Amdahl, Cecilie Delphin & Kvalem, Ingela Lundin (2024). Fatigue in long-term head and neck cancer survivors: the role of psychological and symptom related factors. Fulltekst i vitenarkiv
• Nygård, Stine; Ivanova, Anna & Fischer, Nantje (2024). Er ufrivillig singelhet egentlig et mannsproblem? Fulltekst i vitenarkiv
• Ivanova, Anna (2023). Sexual health concerns and daily functioning in partnered long-term head and neck cancer survivors. Fulltekst i vitenarkiv
• Ivanova, Anna & Stoltze, Kaspara Aavik (2023). Frisør Henrikke (30) mistet håret: − Jeg ble både stresset og redd. [Journal]. VG. Fulltekst i vitenarkiv
• Bogen, Annika Celin & Ivanova, Anna (2023). Hvorfor er hår så viktig for oss? [Internet]. ung.forskning.no. Fulltekst i vitenarkiv
• Ivanova, Anna & Kvalem, Ingela Lundin (2023). Assessing The Relationship Between Genital Self-Image, Self-Objectification, Social Media Use And Genital Cosmetic Surgery In Adult Norwegian Women. Fulltekst i vitenarkiv
• Ivanova, Anna; Amdal, Bente Cecilie Delphin & Kvalem, Ingela Lundin (2023). Are Late Head And Neck Area Symptoms Connected To Sexual Interest And Enjoyment In Long-Term Head And Neck Cancer Survivors? The Role Of Symptoms, Body Image Perception And Subjective Health. Fulltekst i vitenarkiv
• Ivanova, Anna (2023). Body image post cancer treatment. Fulltekst i vitenarkiv
• Ivanova, Anna (2022). Body image and sexuality after treatment for head and neck cancer. Fulltekst i vitenarkiv
• Ivanova, Anna; Kvalem, Ingela Lundin & Amdal, Cecilie Delphin (2022). Body image concerns in long-term head and neck cancer survivors: associations with physical, emotional and social functioning. Fulltekst i vitenarkiv
• Ivanova, Anna (2026). Long-Term Survivorship after Head and Neck Cancer: Psychosocial Outcomes Related to Body Image, Sexuality, and Work. Universitetet i Oslo. Fulltekst i vitenarkiv Vis sammendrag

  Survival after head and neck cancer (HNC) has improved, creating a growing population living many years beyond treatment. Even after acute toxicities subside, late survivorship may be marked by visible and functional late effects that affect psychosocial well-being and everyday roles. This thesis examines psychosocial late effects among long-term HNC survivors treated at Oslo University Hospital and assessed more than five years after treatment. Across three papers, it addresses outcomes central to quality of life and long-term participation, cancer-related body image concerns, sexuality-related problems (sexual interest and sexual enjoyment), and long-term work disability, and evaluates whether these challenges are mainly linked to tumor and treatment history or are better explained by survivors’ current symptom burden and functioning within a biopsychosocial framework. The thesis is based on a cross-sectional survivorship study conducted in 2018–2020. Eligible participants were adults treated for HNC at Oslo University Hospital in 2006 2012 who were at least five years post-treatment at assessment. Participants completed validated patient-reported outcome measures and attended a hospital assessment. Analytic samples included 258 participants in the body image and sexuality papers and 251 participants in the work disability paper, with predictive analyses restricted to a working-age subset of 145 survivors. Outcomes and correlates were assessed using the EORTC QLQ-C30 (physical, cognitive, emotional, and social functioning), the EORTC QLQ-HN35 (HNC-specific symptoms and sexuality items), the Body Image Scale, and the Chalder Fatigue Questionnaire. Body image concerns were divided into three groups (no concerns, mild-to-moderate concerns and body image distress) and examined using multinomial logistic regression. Sexual interest and enjoyment were examined using hierarchical linear regression. Long-term work disability versus employment was examined using hierarchical logistic regression in the working-age subset. Body image concerns were common: 51% reported mild-to-moderate cancer-related concerns and 9% met criteria for body image distress. In multivariable models, body image distress (vs. no concerns) was associated with living without a partner, treatment with radiotherapy and surgery, worse emotional functioning, and higher oral pain, while mild-to-moderate concerns (vs. none) were linked to greater oral pain and speech problems. Sexuality-related problems were also prevalent, with 34% reporting substantial problems with sexual interest and 37% with sexual enjoyment. In the final multivariable model, lower emotional functioning was the strongest independent correlate, with smaller contributions from lower physical functioning and older age. Work participation analyses showed that long-term work disability affected 33% of working-age survivors. Compared with employed and retired peers, those with long term work disability reported poorer physical, emotional, cognitive, and social functioning and higher oral symptom burden, with many clinically meaningful differences. In predictive models among working-age survivors, lower physical and cognitive functioning and body image distress independently predicted long-term work disability, and blue-collar occupation was an additional risk factor. Treatment variables were generally not independent predictors, but lower disability odds for those treated with chemoradiotherapy plus surgery versus radiotherapy alone were interpreted cautiously due to a very small subgroup size. Overall, the thesis shows that clinically meaningful challenges related to body image, sexual interest and enjoyment, and work disability are prevalent in late HNC survivorship. Across outcomes, survivors’ current functioning and symptom experiences were more consistently related to these challenges than distal clinical factors such as tumor site, stage, or treatment modality, supporting a biopsychosocial understanding of survivorship. The findings suggest that follow-up relying mainly on clinical history may miss survivors with substantial psychosocial burden years after treatment, whereas systematic assessment of patient-reported symptoms and functioning may better identify unmet needs and guide targeted rehabilitation, psychological support, sexual health counselling, and vocational interventions. Because this thesis used cross-sectional design, future longitudinal and interventional studies are needed to clarify temporal pathways and to test whether improving modifiable late effects and emotional functioning leads to better long-term adjustment and participation.

• Ivanova, Anna; Nysæter, Maren Kristin & Fischer, Nantje (2025). Skeives psykiske helse fra tjenesteyteres perspektiv: En kunnskapsoppsummering av psykisk helsearbeideres erfaringer i møte med skeive pasienter. CENSE – Norsk forskningssenter for seksuell helse. ISSN 9788256930012. doi: https:/www.sv.uio.no/psi/forskning/grupper/cense/publikasjoner/skeives-psykiske-helse-fra-tjenesteyteres-perspekt.html. Fulltekst i vitenarkiv Vis sammendrag

  BAKGRUNN Denne rapporten er del to av en todelt kunnskapsoppsummering om skeive og psykiske helsetjenester i Skandinavia og internasjonalt. Formålet er å sammenfatte hva tjenesteytere rapporterer om møter med skeive, og å synliggjøre barrierer og tilretteleggere for bekreftende praksis på tvers av individ-, organisasjons- og strukturnivå. METODE Vi gjennomførte en kartleggingsoversikt (scoping review) med hovedfokus på Norge, Sverige og Danmark, supplert med litteratur fra OECD-land. Søk ble gjennomført i internasjonale databaser i mai 2025 og i målrettede skandinaviske kilder i august 2025. Internasjonalt inkluderte vi fagfellevurderte studier og Ph.d.-avhandlinger, mens den skandinaviske delen også inkluderte rapporter og masteroppgaver på grunn av et begrenset evidensgrunnlag. Referanser ble screenet i Covidence, og data ble systematisert i et uthentingsskjema. Funnene ble analysert med en best-fit framework-analyse forankret i en sosioøkologisk modell med tre nivåer (individ, organisasjon og struktur). RESULTATER Datamaterialet omfattet 35 skandinaviske studier (2010–2025) og 99 internasjonale studier (2020–2025). Funnene viser at tjenesteyteres mulighet til å tilby bekreftende og tilgjengelige psykiske helsetjenester påvirkes av forhold på flere nivåer, og at ansvar ofte blir liggende på enkeltpersoner når organisatoriske og strukturelle rammer er uklare. Vi oppsummerer hovedfunnene på tre nivåer: INDIVIDNIVÅ Studiene beskriver en ujevn kompetanse og varierende faglig selvtillit, særlig knyttet til terminologi og praktiske ferdigheter (for eksempel navn/pronomen og transspesifikke spørsmål) og en bekymring for å gjøre feil. Dette kan bidra til at temaer om seksuell orientering og kjønnsidentitet (SOKI) utsettes eller ikke tas opp før brukeren selv introduserer dem. Strategier som innebærer å behandle alle likt, samt forståelser av SOKI som et privat anliggende, kan stå i et spenningsforhold til minoritetsbevisste perspektiver. Samtidig viser studiene at heteronormative og binære antakelser kommer til uttrykk i behandleres språkbruk og kliniske vurderinger. Etiske dilemmaer handler blant annet om når og hvordan man spør om SOKI, konfidensialitet og risiko for utilsiktet outing. I tillegg oppstår utfordringer knyttet til sensitiv dokumentasjon i journalsystemer med binære kategorier. Samtidig fremheves bekreftende mikropraksiser (inkluderende språk, korrekt navn/pronomen og reparasjon ved feil), men også utfordringer knyttet til risikovurdering, henvisningsterskler og behandlerbelastning, særlig i transforløp. ORGANISASJONSNIVÅ På organisasjonsnivå rapporteres det gjennomgående fravær av eller uklarhet i retningslinjer, rutiner og strukturer for implementering. Dette gjør at inkluderende praksis ofte blir prosjektbasert eller ad hoc-organisert, og dermed avhengig av enkeltpersoner. SOKI er i liten grad integrert i standardmaler, skjema og dokumentasjonsrutiner, og studiene beskriver lite systematisk kompetansebygging. Behov for kontinuerlig, praksisnær opplæring, veiledning og kollegastøtte fremheves, samtidig som tids- og ressursbegrensninger og personalomsetning undergraver langsiktighet. Studiene peker også på barrierer i kapasitet, koordinering og pasientforløp, inkludert fragmentering og portvokting, særlig i transrelatert oppfølging. I tillegg kan binære registrerings- og journalsystemer samt personvernhensyn vanskeliggjøre rutinemessig kartlegging og trygg dokumentasjon. Synlige inkluderingssignaler beskrives som døråpnere, men det understrekes at de er utilstrekkelige dersom de ikke følges av kompetanse, ledelsesforankring og endret praksis. STRUKTURNIVÅ På strukturnivå beskriver studiene hvordan sosial kontekst og strukturelt stigma (heteronormative og binære normer, tabu, frykt for diskriminering og interseksjonelle stigmaer) former både tjenestenes handlingsrom og hjelpsøking. Tjenesteinfrastruktur og systemets navigerbarhet fremheves som sentralt, der sentraliserte strukturer, utydelige henvisningsveier, silotenkning og lange ventetider fremstår som systemiske hindre. Kjønnssegregerte tjenester og plasseringskriterier kan begrense trygghet og tilgang for trans og ikke-binære brukere. Juridiske kjønnskategorier, taushetsplikt og dokumentasjonskrav samt diagnostiske retningslinjer beskrives som førende rammer som strukturerer tilbud og roller i praksis. Videre fremheves begrensede datastandarder for SOKI og ujevn dekning av skeiv tematikk i grunnutdanning. Samtidig beskrives sivilsamfunnsaktører som viktige kompetanse- og støtteressurser i kapasitetsbygging og samarbeid. BIDRAG Rapporten sammenstiller forskningsbasert kunnskap om psykisk helsearbeideres erfaringer i møte med skeive pasienter, med særlig vekt på en skandinavisk kontekst. Vi presenterer et evidensbasert operasjonelt sosioøkologisk rammeverk som kan brukes for å bedre forstå hvordan barrierer og tilretteleggere oppstår på individ-, organisasjons- og strukturnivå, og som eventuelt kan brukes for å planlegge tiltak som ikke legger hele ansvaret på den enkelte behandler. På bakgrunn av funnene gir vi også korte anbefalinger.

• Evje, Jacob; Nysæter, Maren Kristin; Ivanova, Anna; Nygård, Stine; Lock, Lennart & Fischer, Nantje (2025). Skeives helse- søkende atferd: En kunnskapsoppsummering av behov, barrierer og erfaringer i møte med helsetjenesten. CENSE – Norsk forskningssenter for seksuell helse. ISSN 9788256930005. Fulltekst i vitenarkiv

Se alle arbeider i NVA