Strengthening Contraceptive Counseling in Pakistan

Contraception Clinical Trial

Official title:

Strengthening Contraceptive Counseling Services to Empower Clients and Meet Their Needs: Protocol for a Multi-phase Complex Intervention in Pakistan

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT04915885
• Other study ID #: FPC21
• Status: Withdrawn
• Phase: N/A
• Start date: January 2022
• Est. completion date: December 2025

Study information

• Verified date: May 2024
• Source: University of Geneva, Switzerland
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

High-quality contraceptive counseling can strengthen global efforts to reduce the unmet need for and suboptimal use of modern contraceptives. This study aims to identify a package of contraceptive counseling interventions designed to strengthen existing contraceptive services and determine its effectiveness in increasing clients' level of decision-making autonomy and meeting their contraceptive needs.

Description:

Methods The five-phase complex intervention design starts with a pre-formative phase aimed at mapping potential study sites to establish the sampling frame. The two-part formative phase first uses participatory approaches to identify the perspectives of clients, including young people and providers, to ensure research contextualization and address each interest group's needs and priorities; clinical observations of client-provider encounters to document routine care form the second part. The design workshop of the third phase will result in the development of a package of contraceptive counseling interventions. In the fourth and experimental phase, a multi-intervention, three-arm, single-blinded, parallel cluster randomized-controlled trial will compare routine care (arm 1) with the contraceptive counseling package (arm 2) and the same package combined with wider method availability (arm 3). The fifth and reflective phase aims to analyze the package's cost-effectiveness and identify implementation barriers and enablers. The primary outcomes are clients' level of decision-making autonomy and met need for modern contraceptives.

Discussion Applying participatory action research principles in designing, testing, and scaling up effective, affordable, and sustainable counseling interventions could help optimize clients' decision-making autonomy and meet their needs for modern contraceptives in low-resource settings. Recognizing the socio-cultural and health service complexities surrounding contraception, including client-provider power dynamics, the study assumes that engaging key stakeholders, including adolescents, women, men, service providers, and policymakers would be more effective. A set of low-technology interventions will likely affect, at the individual level and in a sustainable way, the knowledge, attitudes, and behaviors of women and couples toward contraceptive counseling and provision. At the health service delivery level, the trial implementation would necessitate a shift in providers' attitudes and accountability toward a systematic integration into their clinical practice of must-have and person-centered counseling components, as well as improved health service organization to ensure the availability of competent staff and diversity of contraceptive choices.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: December 2025
• Est. primary completion date: December 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 15 Years to 49 Years

Eligibility

1. she comes to the family planning clinic with the intention to 1.a. use contraception for the first time in her life (new user), or 1.b. switch from a contraceptive method to another one (switching user), or 1.c. resume a method after not using any in the prior three months (lapse user), or 1.d. discontinue a modern method (discontinuing user);

2. she is not coming for the resupply of a currently used method, such as pills or injectables;

3. she has the intention to continue her follow-up at the health center during the 12-month study follow-up;

4. she does not participate in another study; and

5. she provides informed consent.

Related Conditions & MeSH terms

• Contraception

Intervention

Other:
• Routine care
Routine contraceptive counseling and routine method availability
• Package of contraceptive counseling interventions
The implementation package will be co-designed by providers and clients during the formative and research design phases
• Expanded methods
Expanded range of contraceptive methods as recommended by national policies

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Nguyen-Toan Tran

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in clients' decision-making autonomy	Person-Centered Contraceptive Counseling scale (PCCC), developed and tested by Dehlendorf et al. (2021)	Through study completion, an average of 1 year
Primary	Change in clients' met need for family planning	number of participants who want to avoid a pregnancy and are using a contraceptive method / all participants	Through study completion, an average of 1 year
Secondary	Change in modern contraceptive prevalence	number of participants using a modern contraceptive / all participants	6 months and 12 months post enrollment