Iodine DeficiencyPICkNCT05685056
Nutrition & Food Choices in Early Pregnancy
A study testing Text messages in people with Iodine Deficiency, run by University of Glasgow at 1 site in United Kingdom.
Trial summary
PICk study is a mHealth intervention in women trying to conceive and women up to 14 weeks pregnant, aiming to guide food choices, to achieve the recommended iodine intake through diet. Read more about this study
- Who is it for?
- Ages 18 to 45 years, women onlyHealthy volunteers can take part
- Conditions the study is for
- Iodine Deficiency
- What is being tested?
- Text messages
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 100 participants
- Where
- 1 siteUnited Kingdom
- Study dates
- 25 Mar 2017to 30 Oct 2019
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 45 years
- Women only
- Healthy volunteers accepted
- Adult
Who may be able to join
- Trying to conceive or first trimester pregnant women
- English speaking
- Healthy
Who cannot join
- Abnormal pregnancies
- Known thyroid disorders, renal disease, multiple pregnancies, development of gestational diabetes
- Participation in another trial
- Not owning a mobile phone
- Followed by a dietitian at the time of the trial
- Existing or past eating disorders
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Nutrition and Food Choices in Early Pregnancy - a Nutrition Education Intervention
PICk study is a mHealth intervention in women trying to conceive and women up to 14 weeks pregnant, aiming to guide food choices, to achieve the recommended iodine intake through diet.
Read the detailed description
Iodine is important for the synthesis of thyroid hormones, which are driving normal brain development in fetal and postnatal life.
The required level of iodine intake is 140μg/day and there is not proposed increment for pregnant women from the United Kingdom (UK) Department of Health, in contrast to the World Health Organisation (WHO), EFSA, US Institute of Medicine (IoM) and SANZ, that propose an intake in pregnancy which varies from 200 to 150μg/day. In the UK, based on our previous findings, 60% of women in pregnancy do not meet the 250μg/day WHO recommendation of intake.
Over half mothers and practitioners in the UK were found to be unable to identify correct sources of iodine. However, most women have reported willingness to modify dietary behaviour if they received information related to the importance of iodine in pregnancy.
This intervention focuses on providing information about iodine and its importance in pregnancy that would potentially help women improve their iodine status. The intervention was designed with participants involvement and their views on best way of getting information, informed by in-depth qualitative work.
The hypothesis is that increasing knowledge and awareness about the importance, sources and requirements of iodine during pregnancy will lead to change in practice and increased iodine intake.
Methods:
The study is a randomised controlled trial that lasts for 12 weeks. Women in preconception and in the 1st pregnancy trimester will be recruited and will be randomised either to the control or to the intervention group.
The study involves 3 meeting with the participants, at baseline and after 6 and 12 weeks. For women who try to conceive, if conception occurs within the study period, there is a fourth (optional) meeting in the 12th week of pregnancy.
Participants are informed about the study without getting details of the aim (to increase the iodine status of those in the treatment group). This is in order to decrease any bias and avoid leading participants to self-research the topic of iodine nutrition. Women of both study arms receive standard care and the study will not aim to change this. The treatment group is to receive 1-2 weekly text messages focusing on iodine-rich foods importance, barriers identification and tips with ways to include them in the diet.
Samples collection and analysis:
- Questionnaires (demographic, dietary, knowledge, awareness and intervention assessment questionnaires) will be completed by the participants at the place of recruitment / meeting with the researcher after full instructions by the researcher in visits 1, 2 and 3 (and optional visit 4).
- Participants will be given 12 pots for spot urine samples collection in each visit. They will be asked to collect 10 urine samples over 3-4 days. Urinary iodine and creatinine concentrations will be measured.
- A finger prick dried blood spot sample will be taken from each participant in each visit by the researcher. Thyroglobulin will be measured.
Power calculation:
The primary aim of the study is to decrease the proportion of women not meeting the recommended intake for iodine.
Based on a proportion of 60% of women currently not meeting the 250 μg/day recommended intake 5, a sample size of N=84 in total (42 per group) would allow to detect a decrease in proportion down to 30%. This is achievable based on the % of women with an intake of 150-249 μg/day, who could increase consumption by 100 μg/day (equivalent to a 200ml portion of milk and a 125g portion of yoghurt per day) and therefore meet the threshold. Adjusting for 15% dropout, a sample of 50 per group would be sufficient.
- Conditions
- Iodine Deficiency
- Being tested
- Text messages
- Keywords
- Iodine, Pregnancy, Food choices, Fish, Dairy
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Text messagesBehavioural
Texts with detailed information focusing on nutrition and iodine rich foods specifically, every 3-5 days.
| Study group | Role | What they receive |
|---|---|---|
| Control group | No intervention | The control group will receive no intervention, and will be receiving only text reminders regarding the study, the following visits and study logistics in order to limit dropout rate. |
| Intervention group | Experimental | Intervention will happen with weekly text messages during the study period, focusing on pregnancy nutrition and iodine rich foods. The texts will be based on the taxonomy of behavior change techniques used in interventions, the nudge theory and will be covering themes identified on our previous research. Receives: Behavioral: Text messages |
What is being measured
The primary outcome is the main question the study is designed to answer.
proportion of women not meeting the recommended intake for iodine
measured by validated food frequency questionnaire
Measured: 6 weeks
proportion of women not meeting the recommended intake for iodine
measured by validated food frequency questionnaire
Measured: 12 weeks
Secondary outcomes (8)
iodine awareness
Measured by questionnaire, as a median score
Measured: 6 weeks
iodine awareness
Measured by questionnaire, as a median score
Measured: 12 weeks
Iodine knowledge
Measured by questionnaires, as a median score
Measured: 6 weeks
Iodine knowledge
Measured by questionnaires, as a median score
Measured: 12 weeks
Thyroglobulin concentration
measured by immunoassay
Measured: 6 weeks
Thyroglobulin concentration
measured by immunoassay
Measured: 12 weeks
Change in urinary iodine concentration (from baseline)
measured by colorimetry
Measured: 6 weeks
Change in urinary iodine concentration (from baseline)
measured by colorimetry
Measured: 12 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted13 Jan 2023
- Study start25 Mar 2017
- Primary completion17 Jun 2019
- Study completion30 Oct 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Iodine DeficiencyStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind
- Who is masked
- Participant
- Enrolment
- 100 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Glasgow
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Emilie Combet, University of Glasgow
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05685056
- Sponsor's protocol ID
- 200160090
- Acronym
- PICk
- Status last verified
- Jan 2023
- First submitted
- 30 Oct 2017
- Last updated
- 13 Jan 2023
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 13 Jan 2023. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Nutrition and Food Choices in Early Pregnancy - a Nutrition Education Intervention
- ClinicalTrials.gov ID
- NCT05685056
- Acronym / sponsor ID
- PICk / 200160090
- Conditions
- Iodine Deficiency
- Keywords
- Iodine, Pregnancy, Food choices, Fish, Dairy
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 100 participants (actual)
- Lead sponsor
- University of GlasgowUniversity, hospital or other
- Study start
- 25 Mar 2017 (actual)
- Primary completion
- 17 Jun 2019 (actual)
- Study completion
- 30 Oct 2019 (actual)
- First posted
- 13 Jan 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
PICk study is a mHealth intervention in women trying to conceive and women up to 14 weeks pregnant, aiming to guide food choices, to achieve the recommended iodine intake through diet.
Detailed description
Iodine is important for the synthesis of thyroid hormones, which are driving normal brain development in fetal and postnatal life.
The required level of iodine intake is 140μg/day and there is not proposed increment for pregnant women from the United Kingdom (UK) Department of Health, in contrast to the World Health Organisation (WHO), EFSA, US Institute of Medicine (IoM) and SANZ, that propose an intake in pregnancy which varies from 200 to 150μg/day. In the UK, based on our previous findings, 60% of women in pregnancy do not meet the 250μg/day WHO recommendation of intake.
Over half mothers and practitioners in the UK were found to be unable to identify correct sources of iodine. However, most women have reported willingness to modify dietary behaviour if they received information related to the importance of iodine in pregnancy.
This intervention focuses on providing information about iodine and its importance in pregnancy that would potentially help women improve their iodine status. The intervention was designed with participants involvement and their views on best way of getting information, informed by in-depth qualitative work.
The hypothesis is that increasing knowledge and awareness about the importance, sources and requirements of iodine during pregnancy will lead to change in practice and increased iodine intake.
Methods:
The study is a randomised controlled trial that lasts for 12 weeks. Women in preconception and in the 1st pregnancy trimester will be recruited and will be randomised either to the control or to the intervention group.
The study involves 3 meeting with the participants, at baseline and after 6 and 12 weeks. For women who try to conceive, if conception occurs within the study period, there is a fourth (optional) meeting in the 12th week of pregnancy.
Participants are informed about the study without getting details of the aim (to increase the iodine status of those in the treatment group). This is in order to decrease any bias and avoid leading participants to self-research the topic of iodine nutrition. Women of both study arms receive standard care and the study will not aim to change this. The treatment group is to receive 1-2 weekly text messages focusing on iodine-rich foods importance, barriers identification and tips with ways to include them in the diet.
Samples collection and analysis:
- Questionnaires (demographic, dietary, knowledge, awareness and intervention assessment questionnaires) will be completed by the participants at the place of recruitment / meeting with the researcher after full instructions by the researcher in visits 1, 2 and 3 (and optional visit 4).
- Participants will be given 12 pots for spot urine samples collection in each visit. They will be asked to collect 10 urine samples over 3-4 days. Urinary iodine and creatinine concentrations will be measured.
- A finger prick dried blood spot sample will be taken from each participant in each visit by the researcher. Thyroglobulin will be measured.
Power calculation:
The primary aim of the study is to decrease the proportion of women not meeting the recommended intake for iodine.
Based on a proportion of 60% of women currently not meeting the 250 μg/day recommended intake 5, a sample size of N=84 in total (42 per group) would allow to detect a decrease in proportion down to 30%. This is achievable based on the % of women with an intake of 150-249 μg/day, who could increase consumption by 100 μg/day (equivalent to a 200ml portion of milk and a 125g portion of yoghurt per day) and therefore meet the threshold. Adjusting for 15% dropout, a sample of 50 per group would be sufficient.
Study design
- Primary purpose
- Supportive care
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Control group | No intervention | –The control group will receive no intervention, and will be receiving only text reminders regarding the study, the following visits and study logistics in order to limit dropout rate. |
| Intervention group | Experimental | Behavioral: Text messagesIntervention will happen with weekly text messages during the study period, focusing on pregnancy nutrition and iodine rich foods. The texts will be based on the taxonomy of behavior change techniques used in interventions, the nudge theory and will be covering themes identified on our previous research. |
Who may qualify
- Ages
- 18 to 45 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (3 listed)
- Trying to conceive or first trimester pregnant women
- English speaking
- Healthy
Key exclusion criteria (6 listed)
- Abnormal pregnancies
- Known thyroid disorders, renal disease, multiple pregnancies, development of gestational diabetes
- Participation in another trial
- Not owning a mobile phone
- Followed by a dietitian at the time of the trial
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Text messagesTexts with detailed information focusing on nutrition and iodine rich foods specifically, every 3-5 days. | Behavioural | Intervention group |
Primary outcome
proportion of women not meeting the recommended intake for iodine
Time frame: 6 weeks
measured by validated food frequency questionnaire
proportion of women not meeting the recommended intake for iodine
Time frame: 12 weeks
measured by validated food frequency questionnaire
8 secondary outcomes
iodine awareness
Time frame: 6 weeks
iodine awareness
Time frame: 12 weeks
Iodine knowledge
Time frame: 6 weeks
Iodine knowledge
Time frame: 12 weeks
Thyroglobulin concentration
Time frame: 6 weeks
Thyroglobulin concentration
Time frame: 12 weeks
Change in urinary iodine concentration (from baseline)
Time frame: 6 weeks
Change in urinary iodine concentration (from baseline)
Time frame: 12 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 13 Jan 2023.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Text messages in people with Iodine Deficiency, run by University of Glasgow at 1 site in United Kingdom.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 13 Jan 2023. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United Kingdom. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
proportion of women not meeting the recommended intake for iodine (time frame: 6 weeks). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Jan 2023.