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Development and feasibility testing of a "consumer questions" program to increase health literary and empower consumers to participate in decisions about their health.

Development and feasibility testing of a "consumer questions" program to increase health literary and empower consumers to participate in decisions about their health.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12610001055099
Acronym
Consumer Questions Program (CQP) Health literacy/empowerment Project
Enrollment
120
Registered
2010-12-01
Start date
2012-07-11
Completion date
2012-12-11
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Aims To explore the feasibility and implementation issues of a program to train consumers to use simple consumer questions to enhance their understanding and decision-making in a clinical consultation. Specific aims i) To develop and produce a program to train and support consumers to use consumer questions (the Consumer Questions Program CQP) to elicit information for decision making and to integrate this information with their personal preferences, and; ii) To test the feasibility of consumers using this program in FPNSW consultations. Research questions The effects of the program results on: 1) consumers' knowledge of the questions 2) consumers' understanding of when and why they might want to ask the questions 3) consumers' willingness to ask the questions in the consultation 4) consultation processes, particularly in consultation length and complexity Health professionals' reactions to the questions will also be examined.

Interventions

This trial will be conducted in two stages: Stage 1: Development of the Consumer Questions Program (CQP). This is the intervention which will be tested in Stage 2. Participants: a) Clinical staff focus groups (health professionals and clinic staffs at Family Planning NSW b) Consumer focus groups (clients at Family Planning NSW) Outcome: thematic analysis to identify themes and sub-themes within the data (audio-records transcriptions) Stage 1 will take 1-4 months Stage 2: A feasibility Study

This trial will be conducted in two stages: Stage 1: Development of the Consumer Questions Program (CQP). This is the intervention which will be tested in Stage 2. Participants: a) Clinical staff focus groups (health professionals and clinic staffs at Family Planning NSW b) Consumer focus groups (clients at Family Planning NSW) Outcome: thematic analysis to identify themes and sub-themes within the data (audio-records transcriptions) Stage 1 will take 1-4 months Stage 2: A feasibility Study. Testing of the intervention: The Consumer Questions Program. The Consumer Questions Program (CQP) to train consumers to use the consumer questions. The program includes providing participants with four components: i) a 2-5 min CQP DVD ii) a consultation summary sheet iii) a consumer questions reminder card iv) a CQP pamphlet, including website address to access the DVD and the supporting information online The intervention will be delivered once to participants by a research officer/nurse when they attend the clinic. Client participants will complete questionnaires for data collection at 3 time points. Prior to consultation (T1), immediately post consultation ( T2) and 2 weeks post consultation (T3) Participants: a) Clinical staff (health professionals and clinic staff) at Family Planning NSW b) Clients at Family Planning NSW Primary outcomes will be measured from participants' report: a) proportion of client participants who report asking the questions in the consultation b) qualitative data about the experience of asking the questions and use of the information obtained from the doctor as a result of asking the questions. Secondary outcomes: c) proportion of clients who report viewing the CQP video d) Proportion of clients who report accessing the online information e) length of consultation f) access to study online resource monitored by URL address hits g) qualitative data from the health professional log books h) data from the consultation summary sheets completed by client participants. We anticipate Stage 2 will take 5 months to complete all data collection and analysis.

Sponsors

Dr Heather Shepherd
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Primary purpose
Treatment

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1) Women aged equal to or older than 18 years 2) English language fluency

Exclusion criteria

Clients who require an interpreter will not be eligible

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026