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PTSD Coach Study

A counsellor-supported ‘PTSD Coach’ intervention versus enhanced Treatment-as-Usual in a resource-constrained setting: A randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
PACTR
Registry ID
PACTR202108755066871
Enrollment
60
Registered
2021-08-23
Start date
2021-08-30
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Mental and Behavioural Disorders

Interventions

PTSD Coach Counsellor Supported
Enhanced Treatment as Usual

Sponsors

Faculty of Medicine and Health Sciences Stellenbosch Unviersity
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Participants (18 - 65 years) must be able to read and understand English, able to provide written informed consent, and able to attend weekly sessions (active study procedures and follow-ups) at the Faculty of Medicine and Health Science during office hours (Monday – Friday, 08:00 – 17:00). Basic English skills (trained volunteer counsellor in the event that they struggle with language and or technical aspects) Current diagnosis of PTSD Participants using psychotropic medications will be required to have been on a stable dose for at least 2 months before their pre-intervention assessment (T0)

Exclusion criteria

Exclusion criteria: Participants with active alcohol or drug use disorder (past 6 months). High risk for suicide Presence of an organic disorder or cognitive impairment that will compromise uptake of the intervention. Participants will be withdrawn from the study if (i) there is a serious adverse event where the risks of continued participation outweigh the benefits; (ii) a participant is not capable of continuing the study (e.g., relocation) or (iii) a participant voluntarily decides to discontinue the study (withdraw).

Design outcomes

Primary

MeasureTime frame
To assess and compare the change in PTSD symptoms over the course of treatment and follow-up between the intervention arms (PTSD Coach-CS and e-TAU).

Secondary

MeasureTime frame
To assess and compare the change in anxiety, and depression over the course of treatment and follow-up between the intervention arms. To assess and compare neurocognitive function alterations over the course of the intervention between the two arms. To track hair cortisol levels as a long-term neuroendocrine marker of PTSD symptom severity and treatment response between two treatment arms. To gather qualitative feedback from participants about their use of PTSD Coach to augment the quantitative findings.

Countries

South Africa

Contacts

Public ContactErine Brocker

PhD Candidate

erineb@sun.ac.za27219389587

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026