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Completed

NCT Number: NCT05681559

Investigation of Medical Management to Prevent Episodes of Diverticulitis Trial

This is a randomized trial (n=75) of a Mediterranean style Food Pattern and versus standardized guidance on fiber intake for patients with diverticulitis to evaluate the feasibility of this dietary intervention including willingness to randomize and adherence to a Med-style dietary pattern. The investigators will employ state-of-the-art behavioral interventions in the form of electronic feedback to improve health-related behaviors and support dietary customization based on participants' budget, dietary preferences, and restrictions. The investigators will also examine plasma inflammatory biomarkers (interleukin-6, interleukin-10, and interleukin-1β) and fecal calprotectin at baseline, 6, and 12 months.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Harborview Medical Center

Seattle, Washington, 98104, United States

About this study

This is a feasibility-focused, patient-level randomized trial of an intervention promoting the United States Department of Agriculture (USDA) Healthy Med-Style food pattern versus standardized guidance on fiber intake (standard educational materials related to a high-fiber diet) in patients with a history of diverticulitis. This trial will assess and address barriers to the eventual large-scale trial and lay groundwork for that trial that will focus on the risk of recurrent diverticulitis and other clinical outcomes. The investigators will also compare changes in serum and stool biomarkers of inflammation that are proximal endpoints in the causal path relating a Mediterranean diet pattern's anti-inflammatory properties and recurrence of diverticulitis.

Participants randomized to the USDA Mediterranean-style Food Pattern Arm (called Medi for all) will have access to a "toolbox" that includes education materials (e.g., food pattern tables according to daily caloric intake), recipes, grocery lists, group-based online dietary support, feedback, and reminders to encourage dietary change. Recipes and grocery lists can be individualized to a participant's food budget and preferences. Materials will be available in print and Web-based. This state-of-the art intervention will then use electronic feedback in the form of nudge messages designed to motivate participants to sustain or improve adherence to the Med-style Food Pattern. Every two weeks, participants in the intervention arm will be prompted via a digital online platform (analog also available) to complete the 14-item Mediterranean Diet Assessment Score (MEDAS) (an adapted version of the MEDAS Score previously used in the Prevencion con Dieta Mediterranea [PREDIMED study]) for the purpose of providing timely, individual feedback on diet adherence (not for assessing adherence to the diet pattern). The MEDAS score will be calculated via the online digital platform and ranked according to 3 cutpoints: ≤7, 8-9, or ≥10. Patients will be encouraged to achieve a score of ≥10 which is considered high adherence. The platform will then offer feedback based on the levels of self-reported adherence to the diet including self vs. peer comparisons and support resources. Nudge messages will utilize information from a baseline assessment of participants' dietary attitudes and beliefs about which food groups within a Med-style food pattern they perceive to be most within their control. Ultimately, this approach will enable us to provide participants with dietary information and services that support adherence by accounting for attitudes, norms, and perceived control. The extent of interaction with the online platform will be assessed bi-weekly; degree of adherence to the USDA Med-style food pattern; and engagement in dietician services will be assessed at quarterly intervals.

Participants randomized to the High Fiber Diet Arm will be given commonly used patient education pamphlet, describing fiber and high-fiber foods, the rationale for increasing fiber intake, and ways patients can promote greater intake. Based on prior observational studies of incident diverticulitis, at least 25 grams/day of fiber will be recommended for participants.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adult ≥18 years;
  • Patients presenting (or recently presented) to gastroenterologist or surgeons or accessing study website after recovery from an episode of diverticulitis (within the prior 18 months), either the index episode or recurrent.
  • Ability to provide written informed consent in English.

Exclusion criteria

  • Unable or unwilling to return for specimen collection visits or be contacted for and/or complete research surveys;
  • Currently incarcerated in a detention facility or in police custody (patients wearing a monitoring device can be enrolled) at baseline/screening;
  • Last episode of acute diverticulitis currently unresolved (i.e., on antibiotics for diverticulitis; drain in place);
  • Intolerance/allergy to the main components of the Med-style food pattern;
  • Surgery for diverticulitis within past 6 months without an episode of diverticulitis post-surgery;
  • Planned elective surgery in next 6 months

Treatment and study plan

Medi for All

Behavioral

Please see description of Medi for All arm

Standard Fiber Supplementation

Dietary Supplement

Please see description of Fiber Supplementation arm

Primary outcomes

  1. Willingness to enroll

    Time frame: through study completion, over a period of 2 years

    Number of randomized participants out of number approached

  2. Adherence to Med-Style Food Pattern

    Time frame: through study completion, over a period of 12 months

    Med-style Pattern score calculated from the Nutrition Assessment Shared Resource Food Frequency Questionnaire

  3. Participant retention

    Time frame: through study completion, over a period of 12 months

    Proportion enrolled and retained at 3, 6, 9 and 12 months

  4. Engagement with nutrition services

    Time frame: Quarterly through study completion, over a period of 12 months

    Number of sessions with dietician

  5. Interaction with online program

    Time frame: Bi-weekly through study completion, over a period of 12 months

    Number of times accessed

Secondary outcomes

  1. Change in Plasma, Interleukin (IL)-6, IL-10, IL-1b, fecal calprotectin

    Time frame: Baseline, 6, 12 months through study completion, over a period of 12 months

    Concentration

  2. Diverticulitis events

    Time frame: Quarterly through study completion, over a period of 12 months

    Self-reported (presumed), subset of those resulting in healthcare utilization (e.g., hospitalization, surgery).

  3. National Surgical Quality Improvement Program (NSQIP)-defined complications, a subset of which are serious adverse events to be reported to Independent Safety Monitor

    Time frame: Quarterly through study completion, over a period of 12 months

    Standardized assessment-serious events defined as death, cardiac arrest, myocardial infarction, pneumonia, progressive renal insufficiency, acute renal failure, pulmonary embolism, deep vein thrombosis, return to operating room, serious site infections

  4. Change in Diverticulitis Quality of Life Survey (DVQOL)

    Time frame: Baseline, 6, 12 months

    A 17-item questionnaire that assesses four domains: symptoms, concerns, emotions, and behavior changes related to diverticulitis, ranging from 0 (best) to 10 (worst)

  5. Change in Gastrointestinal Quality of Life Index (GIQLI)

    Time frame: Baseline, 6, 12 months

    A 36-item questionnaire that assesses five domains: gastrointestinal symptoms, physical function, emotional well-being, social well-being, and perception of medical treatment measured by a single item question. Each item has 5 response choices (i.e., all of the time, most of the time, some of the time, a little of the time, never). In addition, the measure produces an overall QoL score (0-144) where higher numbers indicate greater QoL.

  6. Change in International Physical Activity Questionnaire (IPAQ) short form

    Time frame: Baseline, 6, 12 months

    A validated 7-item questionnaire: moderate and vigorous physical activity, walking, and sitting in the past 7 days. Output is self-reported minutes of moderate and vigorous physical activity as well as walking from which weekly moderate and vigorous physical activity, sitting, and walking can be assessed.

  7. Healthcare utilization

    Time frame: Quarterly through study completion, at 3, 6, 9, 12 months

    Counts of ED/hospital encounters, diverticulitis-related diagnostic/therapeutic interventions

  8. Change in self-reported weight

    Time frame: Baseline, 6, 12 months

    Self-reported weight

Sponsors and collaborators

Lead sponsor

University of Washington

Other

Collaborators

  • National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Registry information

Official study title

Investigation of Medical Management to Prevent Episodes of Diverticulitis (IMPEDE) Trial

Acronym: IMPEDE

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Jan 12, 2023
Registry last updated
Jun 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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