ClinicalTrials.gg
RecruitingNCT07769216Updated Oct 27, 2026

Online Feeding Education for Fathers of Children With Feeding Problems

An interventional study of Online Feeding Awareness Training for Fathers in Feeding Problems, Parent Training and Parent Child Relationship, sponsored by Ankara Medipol University. Recruiting at 1 site in Turkey (Türkiye). Open to male participants, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-10-27.

Sponsored by Ankara Medipol University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Started Aug 2026; still recruiting 2 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
12
Allocation
Not applicable
Sex
Male
01

Study summary

This pilot study aims to investigate the effects of a four-week online feeding awareness training program for fathers of typically developing children aged 3-6 years. The study will examine changes in fathers' parental self-efficacy and feeding attitudes, as well as their children's eating and mealtime behaviors.

The main research question is whether an online awareness training program for fathers can improve parental self-efficacy and feeding attitudes and contribute to positive changes in children's eating behaviors. Outcomes will be assessed at baseline, immediately after the intervention, and at a four-week follow-up.

02

Conditions studied

  • Feeding Problems
  • Parent Training
  • Parent Child Relationship
  • Feeding Behaviors
  • Fathers

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Keywords

  • feeding problem
  • parent training
  • father-child interaction
  • feeding behavior
  • parenting
03

In context

Feeding Behavior

985 studies on the registry are indexed under Feeding Behavior; 178 are open to participants now.

This study's planned enrollment of 12 is below the median of 77 across 700 interventional studies indexed under Feeding Behavior.

Browse Feeding Behavior studies →

Lead sponsor

Ankara Medipol University is the lead sponsor of 56 studies on the registry; 10 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Male
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Fathers aged 18 years or older who have a typically developing child aged 3-6 years.
  • The child has not previously received feeding therapy or occupational therapy intervention.

Exclusion criteria

Exclusion Criteria:

  • Presence of a serious psychiatric condition or a condition that may affect cognitive functioning in either the father or the child.
  • Missing more than one session of the training program.
  • Lack of access to digital devices or the internet.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
12 participants (estimated)

Study arms

  • Experimental
    Online Feeding Awareness Training Group

    Participants in this arm will receive a four-week online feeding awareness training program for fathers. The program consists of four weekly 60-minute group sessions covering: (1) motor, sensory, cognitive, and psychosocial skills related to feeding; (2) sensory processing and sensory strategies for mealtimes; (3) parental feeding attitudes and behavioral strategies; and (4) parental self-efficacy, emotion regulation, and stress management. Each session includes educational content, discussion, a question-and-answer section, and recommendations for home practice.

    Other: Online Feeding Awareness Training for Fathers

Interventions

  • OtherOnline Feeding Awareness Training for Fathers

    The intervention is a four-week online group-based feeding awareness training program developed for fathers of children aged 3-6 years. It consists of four weekly 60-minute sessions delivered via Google Teams. The sessions focus on: (1) motor, sensory, cognitive, and psychosocial skills involved in feeding; (2) sensory processing differences and sensory strategies that can be used before mealtimes; (3) parental feeding attitudes, mealtime routines, positive reinforcement, and behavioral strategies; and (4) parental self-efficacy, emotion regulation, stress management, and brief relaxation and mindfulness strategies. Each session includes educational content, discussion, a question-and-answer section, and recommendations for home practice.

06

What researchers measure

Primary outcomes

  1. Parental Self-Efficacy Scale

    The Parental Self-Efficacy Scale is a 17-item, 7-point Likert-type measure used to assess parental self-efficacy. Each item is scored from 1 (strongly disagree) to 7 (strongly agree), resulting in a total score ranging from 17 to 119. Higher scores indicate greater parental self-efficacy.

    Time frame: Baseline (pre-intervention), immediately after the 4-week intervention (Week 4), and 4 weeks after completion of the intervention (Week 8).

  2. Behavioral Pediatrics Feeding Assessment Scale (BPFAS)

    The Behavioral Pediatrics Feeding Assessment Scale (BPFAS) is a parent-reported measure used to assess children's eating and mealtime behaviors. Items are rated on a 5-point Likert scale ranging from 1 (never) to 5 (always). The Turkish adaptation evaluates the 25 items related to the child's feeding behaviors. Higher scores indicate more problematic eating behaviors and greater feeding difficulties.

    Time frame: Baseline (pre-intervention), immediately after the 4-week intervention (Week 4), and 4 weeks after completion of the intervention (Week 8).

  3. Parental Feeding Style Questionnaire

    The Parental Feeding Style Scale is a 27-item, 5-point Likert-type measure used to assess parents' attitudes and behaviors related to feeding their children. Each item is scored from 1 (strongly disagree) to 5 (strongly agree), with total scores ranging from 27 to 135. Higher scores indicate a greater presence of the corresponding parental feeding style. The Turkish version includes four feeding-style dimensions assessing parental control, guidance, and emotional responses during feeding.

    Time frame: Baseline (pre-intervention), immediately after the 4-week intervention (Week 4), and 4 weeks after completion of the intervention (Week 8).

Secondary outcomes

  1. Participant Satisfaction With the Online Feeding Awareness Training

    An investigator-developed numerical rating questionnaire will be used to assess participants' perceptions of the effectiveness, comprehensibility, and overall satisfaction with the online feeding awareness training. Each item is rated on a 10-point Likert-type scale ranging from 1 (strongly disagree) to 10 (strongly agree).

    Time frame: Immediately after completion of the 4-week intervention (Week 4).

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No — Individual participant data (IPD) will not be shared because participants did not provide consent for their individual-level data to be shared with external researchers. The data will be used only for the purposes described in the approved study protocol and will be kept confidential.

No publications or documents are linked to this record.

09

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Aug 2026 to primary completion in Aug 2026, 0 months.

Of 503 non-industry interventional studies with no phase under Feeding Behavior, half reached primary completion within 14 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 31. This study's 0 months is below that.

Counting every sponsor, half of 515 studies reached it within 14 months; a quarter within 5 and three quarters within 31.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 12, 2026
First posted
Aug 17, 2026
StartActual
Aug 13, 2026
Primary completionActual
Aug 25, 2026
CompletionEst.
Nov 2, 2026
Last update
Oct 27, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Minor edits
Nothing that changes what the study is or who can join. Edited: verification date and date precision
1 update, last Oct 27, 2026
Show all 1 update
  1. Oct 27, 2026
    Minor edits only
    + 2 other changes: verification date and date precision

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07769216
Lead sponsor
Ankara Medipol University
Responsible party
Rukiye Begüm KOCA (Lecturer, PhD, Ankara Medipol University) — Principal investigator
First posted
Aug 17, 2026
Start date
Aug 13, 2026
Primary completion
Aug 25, 2026
Completion
Nov 2, 2026 (estimated)
Last update
Oct 27, 2026

Study contacts

Rukiye Begüm Koca Şentürk, PhD
Contact
rukiye.koca@ankaramedipol.edu.tr
+09535 447 48 49

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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