Effectiveness of Implementing the Adapted Practice Guidelines for Primary Care of Acute Abdomen in Zambia: An Effectiveness-Implementation Hybrid Type 2 Study Design.

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Bergen

About this trial

The study aims 1) to adapt, 2) to develop implementation strategies for and 3) to evaluate the effect of implementing a practice guideline for acute abdomen at primary care level in Zambia. We employ a sequential exploratory mixed method study design. Qualitative and quantitative data from health care workers will be used to adapt a practice guideline developed in a high-income into a low- and middle-income (LMIC) context and to develop strategies for successful implementation. The primary outcome of interest is the prospective change in length of stay in hospital among patients presenting with acute abdomen in the intervention site compared to the control site. The study will address the scarcity of literature on practice guidelines for acute abdomen in the LMIC context. The implementation of an adapted guideline may contribute to a reduction of the morbidity and mortality rates associated with acute abdomen in this setting by increasing management capacity at the primary care level.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Data from all patients 18 year and older with acute abdomen including surgical, gynecological and medical acute abdomen managed at the intervention site and control site will be collected during the study period.

Disqualifiers

All cases of acute abdomen secondary to trauma will be excluded from the study. All patients in the immediate postoperative phase operated from other facilities presenting with acute abdomen.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Practice guidelines for primary care of acute abdomen

    Other intervention

    Adjusted practice guidelines for primary care of acute abdomen will be implemented at the intervention site.

  • No intervention

    Other intervention

    The control site will receive no intervention.

Treatment groups

280 Participants
are divided into 2 treatment groups
Group A: Intervention siteExperimental treatment 1 intervention
Group B: Control siteActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Length of Hospital Stay

The duration of time in days that a patient with acute abdomen stays in the hospital from the day of admission to discharge

Time frame
7 days

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Bergen

Lead sponsor

University of Zambia

Collaborator