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Stepping Stones and Creating Futures Plus Pilot

An Inter-disciplinary Approach to Understanding and Intervening on Contextual Factors That Shape HIV-risk for Young Women and Men in South Africa: Phase 2 - the Feasibility, Acceptability and Potential Effect Size of a Pilot Randomised Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05783336
Enrollment
325
Registered
2023-03-24
Start date
2023-05-24
Completion date
2023-11-28
Last updated
2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intimate Partner Violence, Poverty

Brief summary

The goal of this randomised controlled clinical trial is to test the Stepping Stones and Creating Futures Plus (SSCF+) intervention, in young (18-25 years) people living in urban informal settlements in Durban and rural communities in KwaZulu-Natal, South Africa. The main questions it aims to answer are: * Is the intervention acceptable and feasible * What is the potential effect size on key outcomes of intimate partner violence Participants will be randomised (1:1) to compare SSCF+ and a control arm to see if there are differences between the two on intimate partner violence.

Detailed description

Intimate partner violence is very common in South Africa, particularly urban informal settlements. We have co-developed an intervention, called Stepping Stones and Creating Futures Plus (SSCF+), which will be evaluated in women and men aged 18-25 years living in KwaZulu-Natal, South Africa. This is a pilot randomised controlled trial and as such there is focus on understanding whether the intervention is acceptable (to participants), feasible to deliver, and the potential effect sizes we may see in a full trial.

Interventions

BEHAVIORALStepping Stones and Creating Futures Plus (SSCF+)

Group-based intervention delivered to small friendship networks, by a facilitator.

Sponsors

University of Exeter
Lead SponsorOTHER
Medical Research Council, South Africa
CollaboratorOTHER
University College, London
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Normally resident in the community where recruiting * Aged 18-30 years old * Not in formal employment, or full-time education * Able to communicate in the main languages of the study (English, isiXhosa or isiZulu) * Able to provide informed consent

Exclusion criteria

* Only in the community temporarily * Unable to provide informed consent * Under 18 years of age, or over 31 years old at point of recruitment * Unable to communicate in main study languages

Countries

South Africa

Contacts

PRINCIPAL_INVESTIGATORRachel Jewkes

Medical Research Council, South Africa

PRINCIPAL_INVESTIGATORAndrew Gibbs

University of Exeter

PRINCIPAL_INVESTIGATORJenevieve Mannell

University College, London

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 14, 2026