Table 2.
Summary of the population, area of HIV and interventions considered per study included
Reference and country of origin | Population (number and inclusion criteria) | Area of HIV continuum | Intervention and comparator | Overall article quality |
---|---|---|---|---|
Randomised controlled trial | ||||
Choko et al. (2019)[18] | Population: Male partners of pregnant women who had their first prenatal visit. 1: 1 ratio in all 5 groups were considered, obtaining a total sample of 2,349 individuals | Prevention: male circumcision rate | Intervention: 4 incentive strategies, 3 with financial incentives (assignment of rapid HIV tests with $ 3 and $ 10 conditional fixed incentives and a third incentive based on a $30 lottery) and a strategy with non-financial incentives (quick test + two calls follow-up phone calls) | High |
Country of origin: Malawi | Inclusion: pregnant women who had their first prenatal care appointment | Link to treatment care | Comparator: clinical practice with no financial incentives | |
El-Sadr et al. (2019) | Population and Inclusion: Participants in the HPTN 065 study (El-Sadr et al. 2017) | Care retention (continuity of care) | Intervention: utilisation of individual financial incentives around continuity of care (e.g. attending appointments) and viral suppression | High |
Country of origin: USA | Viral load suppression | Comparator: clinical practice with no financial incentives | ||
Thirumurthy et al. (2019) | Population: 400 participants (203 in the intervention group and 197 in the control group) | Care retention | Intervention: received financial incentives conditional for viral suppression at 6, 12 and 24 weeks, with the value of the incentive to scale from $ 4 to $ 12.5 | Intermediate |
Country of origin: Uganda | Inclusion: aged 18 + , living in one of the four communities considered in the study, with a positive result for HIV, and who were starting or already receiving ART | Adherence to treatment and viral suppression | Comparator: viral load tests and counselling | |
Kadota et al. (2018) | Population: 805 HIV positive individuals recruited at 3 clinics | Link to care and ART initiation | Intervention: two intervention groups:(1) food assistance; (2) money transfers | High |
Country of origin: Tanzania | Inclusion: Adult HIV patients, with food insecurity, and on ART initiation ≤ 90 days before enrolment in the study | Care retention | Comparator: usual care | |
Maughan-Brown et al. (2018) | Population: 84 individuals equally distributed between groups | Link to care and ART initiation | Intervention: usual care + voucher (exchangable for monetary value if ART started in the following 3 months) | Intermediate |
Country of origin: South Africa | Inclusion: HIV-diagnosed adults referred for ART by a mobile health clinic in Cape Town who had never previously had ART | Comparator: usual care (telephone follow-up advice from staff to encourage care promotion) | ||
Mills et al. (2018) | Population: Participants from two rural districts of Uganda, recruited through AIDS centres and home visits to patients who had not visited a centre recently | Prevention | Intervention: unconditional monetary grants, with or without financial advice: Group T1: unstructured grant; Group T2: mental planning + grant | Intermediate |
Country of origin: Uganda | Inclusion: HIV positive, aged between 18 and 60 years old, living in the two rural districts considered | Link to care and ART initiation | ||
Viral suppression | Comparator: Group T3: control (no incentives); and Group T4: expectations / control (participants were told they would receive a monetary grant 12 months after the program started—after the follow-up interview) | |||
Montoy et al. (2018) | Population: 8,715 patients in an urban emergency department (San Francisco) | Testing and screening | Intervention: $ 1 incentives, $ 5 incentives, or $ 10 incentives (each of these groups, with 3 subgroups—opt-in, active choice, opt out test) | High |
Country of origin: USA | Inclusion: aged between 13–64 years; being able to give consent for HIV testing and study inclusion in the study; speak English or Spanish | Comparator: without incentives (also with 3 subgroups—opt-in, active choice, opt out test) | ||
Chamie et al. (2018) | Population: A total of 2,527 participants had complete data and were considered for analysis | Testing and screening | Intervention: (1) incentives included in the loss: participants who had won a prize were later told they would lose that prize if they did not take the test; 2) lottery-based incentives: participants who had an HIV testing automatically enter a lottery and had the opportunity to instantly win prizes | High |
Country of origin: Uganda | Inclusion: adult men (≥ 18 years old) referred to in the censuses, who lived in the community for ≥ 6 months in the year prior to referral and who had no intention of leaving the community in the following 3 months | |||
Alsan et al. (2017) | Population: 110 HIV-infected adults with a plasma viral load (pVL) > 200 copies / mL despite ART (n = 21 adults in the professional visit incentive group; n = 19 adults in the choice incentive group, n = 70 in the passive control group) | Care retention and adherence to treatment | Intervention: (1) incentive group to visit professionals (US $30 incentive after participating in each scheduled visit to professionals); (2) incentive choice group (commitment contract that makes the payment of US $ 30 conditioned both to participation in the scheduled visits of professionals and adherence to ART) | Intermediate |
Country of origin: USA | Inclusion: the HIV-1 plasma RNA viral load over > 200 copies / mL measured in the previous 18 months and at least 6 months after starting the current ART regimen | Viral suppression | Comparator: routine care without any incentive | |
El-Sadr et al. (2017) | Population: 1,159 HIV patients (new HIV patients or unknown to healthcare in the past 12 months) were recruited to assess adherence to healthcare (389 in New York and 770 in Washington) and a total of 16,208 patients with HIV (established HIV patients) were recruited to assess viral load suppresion (9,703 in New York and 6,505 in Washington) | Care retention and adherence to treatment | Intervention: healthcare providers were randomised to provide financial incentives to HIV patients. Participants received: (1) a $ 125 voucher ($ 25 for conducting CD4 tests and $ 100 for an HIV planning medical consultation); and / or (2) $ 70 voucher for HIV testing with suppressed viral load (CD4 < 400 copies / mL), with a maximum of one voucher each quarter | High |
Country of origin: USA | Inclusion: Health providers, not their users, were randomised to the intervention and control group | Viral suppression | Comparator: healthcare providers randomised not to give financial incentives (i.e. follow usual care) | |
Stitzer et al. (2017) | Population: post hoc secondary analysis of the HOPE study (Metsch et al., 2016) | Care retention | Intervention: please refer to Metsch et al. (2016) – see below | Intermediate |
Country of origin: USA | Inclusion: please refer to Metsch et al. (2016) – see below | Comparator: please refer to Metsch et al. (2016) – see below | ||
Metsch et al. (2016) | Population: 801 patients with HIV and substance abuse from 11 hospitals | Viral suppression | Intervention: 2 groups: (1) received a structured patient navigation intervention (up to 11 care coordination sessions, with case management and motivational interview techniques over 6 months) (n = 266); (2) structured patient navigation intervention and financial incentives (up to US $ 1,160) (n = 271) | High |
Country of origin: USA | Inclusion: several criteria are mentioned (e.g. inpatients with HIV infection, being 18 years or older) | Comparator: usual care (n = 264) | ||
de Walque et al. (2015) | Population: HIV patients from different clinics randomised to the intervention and control group | Testing and prevention | Intervention: randomised health care providers (n = 10) received incentives in the field of HIV prevention and treatment (organisational incentive) | Intermediate |
Country of origin: Rwanda | Inclusion: Health care providers that treat patients with HIV infection were randomised | Comparator: randomised health care providers to receive an increase in fixed financing equivalent in magnitude to the intervention model (n = 14) | ||
de Walque et al. (2012) | Population: 2,399 participants between the ages of 18 and 30 from certain ten geographical areas in Tanzania | Prevention | Intervention: two groups, with varying magnitude of incentive: (1) group with low level of incentive ($ 30 total incentive) and (2) group with high level of incentive ($ 60 total incentive). In both cases, the incentive was conditional on a negative test result every 4 months | Intermediate |
Country of origin: Tanzania | Comparator: usual care with no incentives | |||
Barnett et al. (2009) | Population: 86 individuals, with 66 of these with less than 80% adherence to their ART (34 were allocated to the incentive group with a voucher and 32 were allocated to the comparison group) | Care retention and adherence to treatment | Intervention: incentives with vouchers conditional on adherence to ART. The participant could accumulate earnings before choosing a redeemable voucher for purchases, meals or other | Intermediate |
Country of origin: USA | Inclusion: HIV positive patients on methadone maintenance were eligible if they had been taking ART for at least 1 month | Comparator: weekly lottery was used to reduce dropouts among these participants, (3 in 1 chance of winning a small prize and a 350 in 1 chance of winning $80) | ||
Non-randomised prospective study | ||||
Belenky et al. (2018) | Population: a total of 801 women with HIV and different insurance coverage | ART initiation | Intervention: change to the HIV drug financing model: HIV patients with Medicare / Medicaid double coverage, eligible for the transition to the Medicare Part D system in Jan 2006 | High |
Country of origin: USA | Inclusion: women with HIV with at least one HIV follow-up visit; and included in the Medicare / Medicaid program (double coverage) or only in the Medicaid program with adherence to the Medicare Part D program in January 2006 | Viral suppresion | Comparator: HIV patients and Medicaid coverage and no additional insurance in 2005 | |
Brantley et al. (2018) | Population: HIV patients recruited from 3 clinics in the State of Louisiana in the USA (n = 2076) | Adherence to ART | Intervention: assigning multiple individual card incentives: an initial incentive of $ 50, $ 20 for each medical consultation, $ 10 for each laboratory exam, $ 10 for referral to the service and $ 75 for keeping the viral load below the target (n = 2076) | Intermediate |
Country of origin: USA | Inclusion: HIV patients with at least one laboratory test in the year prior to recruitment | Viral suppresion | Comparator: HIV patients who did not integrate the individual incentive model | |
Rajkotia et al. (2017) | Population: 134 health institutions | Prevention | Intervention: organisational incentive model based on performance-based unit payments | High |
Country of origin: Mozambique | Inclusion: health institutions in the provinces of Nampula (north) and Gaza (south), certified by the Government of Mozambique to provide ART and prevention of mother-to-child transmission of HIV | Comparator: only standard input-based financing (without performance-based incentives) | ||
Foster et al. (2014) | Population: A total of 11 adults with an average age of 19 years and 8 months | Viral load suppresion | Intervention: allocation of individual financial incentives in combination with consultation with a clinical psychologist and / or specialist nurse trained in motivational interviewing techniques (up to a total incentive of £ 200 conditional on sustained reductions in viral load and participation in motivational consultation) | Low |
Country of origin: UK | Inclusion: patients with vertically acquired HIV who transitioned from paediatric services to adults with: CD4 count < 200 cells / µL); not taking ART despite several attempts to start treatment; and with the intention of resuming ART | Comparator: no comparator / control group | ||
Modelling studies (cost-effectiveness studies) | ||||
Wagner et al. (2020) | Population: Patients in the emergency department of the Zuckerberg San Francisco General Hospital and Trauma Centre (Montoy et al., 2015) | Prevention | Intervention: small immediate financial incentives, opt-in / opt-out testing and a combination of both schemes | Intermediate |
Country of origin: USA | Inclusion: age between 13–64 years; being able to give consent for HIV testing and the study; speak English or Spanish. Patients with previous HIV diagnosis were excluded | Testing and screening | Comparator: standard option (offering tests through an inclusion or exclusion regime) | |
Adamson et al. (2019) | Population: HIV patients in the Bronx (New York) and Washington DC (n = 16.208) | Viral load suppression | Intervention: $ 70 vouchers for patients with CD4 viral load < 400 copies / mL | High |
Country of origin: USA | Inclusion: HIV patients who received incentives based on a randomised clinical trial (El-Sadr et al. 2017) | Comparator: no comparator / control group was considered | ||
Stevens et al. (2018) | Population: participants in the Link4Health randomised clinical trial | Prevention | Intervention: (1) Point-of-care CD4 + count testing; (2) Accelerated ART initiation; (3) Mobile phone appointment reminders; (4) Care and prevention package including commodities and informational materials; and (5) Non-cash financial incentive | High |
Country of origin: Swaziland | Testing and screening | Comparator: usual care with no incentive | ||
Heymer et al. (2012) | Population: Based on HIV epidemiology in South Australia (data from 2004 to 2008) | Prevention | Intervention: removal of negative financial incentive (co-payment) | High |
Country of origin: Australia | Inclusion: not mentioned | Comparator: usual care with co-payments |