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Completed

NCT Number: NCT02269956

Mealtime Symptoms in Dementia

The purpose of this study is to combine current evidence-based guidelines with adaptive leadership (AL) training to assist nursing staff to navigate the delicate balance of necessary technical and adaptive work to improve problematic dementia-related mealtime symptoms.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Currently, basic training programs do not adequately teach nursing home (NH) staff to handle behavioral symptoms at mealtime that typically accompany dementia. When persons with dementia (PWD) exhibit mealtime symptoms (e.g. turning away of the head, pushing food away), these symptoms may be interpreted as lack of interest in eating, and feeding attempts ceased. This misinterpretation poses serious health risks to PWD including under-nutrition and increased risk for more aggressive medical treatment (e.g. feeding tube). The Aims of this study are to: 1) Identify the adaptive leadership challenges of NH staff for alleviating mealtime symptoms for PWD; 2) Determine NH staff evaluation of a dementia feeding skills training program that combines adaptive leadership approaches with technical approaches to mealtime symptoms; and 3) Conduct a 12-week feasibility study implementing this dementia feeding skills training program with NH staff, linking training to resident outcomes. Focus groups will be conducted in four NHs during which NH staff will describe adaptive challenges around: mealtime symptom recognition, communication patterns, typical responses to mealtime symptoms, and feelings when interventions are met with success or failure. Focus group interviews will be transcribed and content analysis conducted. Findings from the focus group interviews will be used to revise a dementia feeding skills program. The revised training program will be evaluated by NH staff to determine how NH staff perceives the coaching intervention, and if case scenarios are realistic and compatible with current workplace practices. The training program will be implemented in two skilled NHs over a five week period. NH staff outcomes include mealtime knowledge and self-efficacy. Through meal observations, NH staff will be assessed for time spent assisting with feeding and feeding skill behaviors; and PWD outcomes assessed by quantifying meal intake and aversive feeding behaviors. Findings from this study will describe adaptive leadership challenges for NH staff, revise and implement a training program teaching NH staff adaptive and technical interventions for alleviating mealtime symptoms for PWD in the NH setting.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

Nursing Home staff participants must be:

  • 18 years of age or older,
  • able to read and write English,
  • willing to sign informed consent,
  • employed as a Registered Nurse, Licensed Practical Nurse, Certified Nursing Assistant, part of the Nursing Home Administration team, or part of the therapy team.

Persons With Dementia participants must be:

  • a resident (> 6 wks) of NH,
  • 60+ years of age,
  • able to speak English in order to give assent,
  • have a positive Minimum Data Set 3.0 for: Active disease diagnosis of Alzheimer's Disease or dementia,
  • require extensive assistance to total dependence for eating,
  • have a Brief Interview for Mental Status (BIMS) score ranging from 0-12 (lower score indicates greater cognitive impairment)37, and
  • have a legally authorized representative (LAR) able to read English in order to provide informed consent for the PWD.

Exclusion criteria

PWD:

  • Minimum Data Set 3.0 positive for: Human Immunodeficiency Virus (HIV) Infection, Parkinson's Disease, and/or Traumatic Brain Injury,
  • any swallowing disorder,
  • parental/ IV feedings, or presence of a feeding-tube;
  • any significant auditory or visual impairment that would prevent the PWD from hearing/seeing verbal/visual cues.

Treatment and study plan

12 week feasibility study

Behavioral

: At baseline, weeks 6 and 12, dementia feeding skills knowledge and self-efficacy tests will be administered, meal observations of nursing staff assisting PWD with meals will be video recorded for three meals over two days, and a medical record review will be conducted to ascertain technical and adaptive interventions also in place for the PWD (e. g., high density protein supplements, appetite stimulant medications, weighing, diet texture modifications). After baseline data is collected, the training program will delivered in five weekly modules with group coaching sessions completed the same week

Primary outcomes

  1. Change in Feeding Skills Knowledge Test

    Time frame: Baseline (before training program), Week 6 (after training program), and Week 12

    10 item multiple choice test administered in paper/ pencil format to nursing staff assisting with feeding persons with dementia (Scores range from 0-10)

  2. Change in Feeding Skills Self-Efficacy Test

    Time frame: Baseline (before training program), Week 6 (after training program), and Week 12

    10 items with likert scale response administered to nursing home staff

Secondary outcomes

  1. Functional Rating Scale for Symptoms in Dementia

    Time frame: 12 weeks

    14 categories related to functional ability of PWD (e. g., eating and dressing ability, emotionality, memory). Each category scores 0-3. Totals range from 0-42; higher score indicative of greater impairment

  2. Brief Inventory of Mental Status

    Time frame: 12 weeks

    Part of Minimum Data Set (MDS) 3.0. 5 sections of cognitive ability questions scored 0-2; scores of 0-12 considered moderate to severe cognitive impairment.

  3. C3P Feeding Skills Checklist

    Time frame: 12 weeks

    Multi-item checklist of feeding skill behaviors grouped around changing the person, place or people. Each section is given numerical value.

  4. Food Intake Record

    Time frame: Collected for 3 meals over 2 days at Baseline, Week 6 and Week 12

    Meal intake documented by pre-post meal tray weight as well as documentation of hand feeding techniques used during the meal.

  5. Edinburgh Feeding in Dementia (EdFED) scale

    Time frame: Collected for 3 meals over 2 days at Baseline, Week 6 and Week 12

    Scale measuring aversive feeding behaviors on a 0-20 scale of 10 items. Higher scores equal more aversive feeding behaviors.

  6. Time Spent Feeding

    Time frame: Collected for 3 meals over 2 days at Baseline, Week 6 and Week 12

    Time spent feeding was measured in hours and minutes via stopwatch.

Sponsors and collaborators

Lead sponsor

Duke University

Other

Registry information

Official study title

Mealtime Symptoms in Dementia: Adaptive Leadership Approaches

Important dates

Study start
2014
Primary completion
2016
Study completion
2016
First posted
Oct 21, 2014
Registry last updated
Apr 4, 2017

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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