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다발성 경화증 관련 피로 연구를 치료하기 위한 식이 접근법 (Waves)

2026년 9월 15일 업데이트: Terry L. Wahls

The purpose of this study is to compare the effect of the Swank Diet (low saturated fat) and the Wahls Elimination Diet (modified paleo) on fatigue levels in individuals with relapsing-remitting multiple sclerosis who have documented fatigue. Participants will follow their usual diet for 12 weeks and then be randomly assigned to follow one of the two diets for 24 weeks.

연구 개요

상세 설명

The purpose of this study is to compare the effect of the Swank Diet (low saturated fat) and the Wahls Elimination Diet (modified paleo) on fatigue levels in individuals with relapsing-remitting multiple sclerosis who have documented fatigue. Participants will follow their usual diet for 12 weeks and then be randomly assigned to follow one of the two diets for 24 weeks. Individuals will continue with their current treatments in addition to following the study diet.

The study requires four visits to the University of Iowa Hospitals and Clinics in Iowa City, Iowa. Visits will be 12 weeks apart. Study activities include fasting blood draws, weighed food records, motor and cognitive testing, physical activity assessment, questionnaires, and daily diet checklists while following the study diet. Some reimbursement available.

연구 유형

중재적

등록 (실제)

95

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 장소

    • Iowa
      • Iowa City, Iowa, 미국, 52242
        • University of Iowa Hospitals and Clinics

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

Inclusion Criteria:

  • Willing to allow your neurologist to sign a letter confirming multiple sclerosis diagnosis and criteria used in diagnosis
  • Relapsing-Remitting Multiple Sclerosis as documented by the McDonald Criteria confirmed by their treating neurologist
  • Fatigue as documented by a Fatigue Severity Scale score of greater than or equal to 4
  • Between the ages of 18 and 70
  • Body Mass Index greater than or equal to 19
  • Ability to shop for and prepare or have someone in the family shop for and prepare home cooked meals according to study diet guidelines
  • Willingness to keep detailed food records
  • Willing to eat a diet that includes more vegetables and excludes many comfort foods such as those made with white flour,
  • Willing to eat a diet that eliminates red meat (beef, pork, lamb, veal) and saturated fats (butter, coconut oil, margarine, hydrogenated oils found in processed foods) to 1 tablespoon per day
  • Must not be pregnant or planning to become pregnant in the next year
  • Willing to eat meat (eg, chicken, turkey, fish)
  • Willingness to follow either the Wahls Elimination diet or the Swank diet
  • Individuals who have had gastric bypass surgery have obtained a signed statement from their physician indicating they are weight stable and a suitable candidate for this study
  • Normal or mild cognitive impairment as measured by the Short Portable Mental Status Questionnaire
  • Willing to have blood drawn
  • Be able to walk 25 feet without support, or with only unilateral support (i.e. cane in one hand)

Exclusion Criteria:

  • Taking insulin or Coumadin
  • Relapse within past 12 weeks
  • Treatment for a cancer (other than skin cancer) currently or in the prior 12 months
  • Diagnosis of heart failure, liver cirrhosis, angina, history of kidney stones, psychiatric disease likely to make adherence to the study interventions more difficult including eating disorders, but excluding depression and anxiety
  • Body Mass Index less than 19
  • Moderate to severe mental impairment as measured by the Short Portable Mental Status questionnaire
  • Inability to shop for and prepare home cooked meals by the subject or a companion
  • Unwillingness to eat meat
  • Participation in another research study that involves multiple sclerosis or other medications, diet, supplement, exercise or other treatments
  • Inability to keep food records with sufficient detail to asses dietary intake or complete study questionnaires
  • Unwilling to have blood drawn
  • Pregnant or planning to become pregnant in the next year

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 무작위
  • 중재 모델: 병렬 할당

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Swank Diet

Individuals randomized to this arm will follow a low saturated fat diet starting at week 12.

A Registered Dietitian Nutritionist (RDN) skilled in motivational interviewing will provide nutrition counseling to study participants to assist them in following the Swank Diet at home. An in-person counseling session will occur at study visits 2 and 3. Five telephone counseling calls will occur between visits 2 and 3. The study participant may contact the RDN with questions at any time during the intervention.

실험적: Wahls Elimination Diet

Individuals randomized to this arm will follow a modified paleolithic diet that eliminates all grains, dairy, eggs, legumes, and nightshade vegetables/spices starting at week 12.

A Registered Dietitian Nutritionist (RDN) skilled in motivational interviewing will provide nutrition counseling using to study participants to assist them in following the Wahls Elimination Diet at home. An in-person counseling session will occur at study visits 2 and 3. Five telephone counseling calls will occur between visits 2 and 3. The study participant may contact the RDN with questions at any time during the intervention.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Change in participant perceived fatigue severity
기간: 12-24 weeks

Participant questionnaire asking about fatigue: Fatigue Severity Scale score - a 9-questions scale ranging from 1 (complete disagreement with the question) to 7 (complete agreement with the questions)

12-24 weeks
Change in participant perceived fatigue severity
기간: 12-36 weeks

Participant questionnaire asking about fatigue: Fatigue Severity Scale score - a 9-questions scale ranging from 1 (complete disagreement with the question) to 7 (complete agreement with the questions)

12-36 weeks
Change in the impact of fatigue on daily life
기간: 12-24 weeks

Modified Fatigue Impact Scale score: Participant questionnaire asking about impact of fatigue impact daily life: Modified Fatigue Impact Scale score. This instrument provides an assessment of the effects of fatigue in terms of physical, cognitive, and psychosocial functioning. The MFIS consists of 21 items. Scoring is based upon a sum of the responses. Total score ranges from 0 to 84.

12-24 weeks
Change in the impact of fatigue on daily life
기간: 12-36 weeks

Modified Fatigue Impact Scale score: Participant questionnaire asking about impact of fatigue impact daily life: Modified Fatigue Impact Scale score. This instrument provides an assessment of the effects of fatigue in terms of physical, cognitive, and psychosocial functioning. The MFIS consists of 21 items. Scoring is based upon a sum of the responses. Total score ranges from 0 to 84.

12-36 weeks

2차 결과 측정

결과 측정
측정값 설명
기간
Change in participant walk speed
기간: 12-24 weeks

6 Minute Walk Test

12-24 weeks
Change in participant walk speed
기간: 12-36 weeks

6 Minute Walk Test

12-36 weeks
Change in gait (walk)
기간: 12-24 weeks

25 foot Walk Test

12-24 weeks
Change in gait (walk)
기간: 12-36 weeks

25 foot Walk Test

12-36 weeks
Change in fine motor function
기간: 12-24 weeks

Pegboard test

12-24 weeks
Change in fine motor function
기간: 12-36 weeks

Pegboard test

12-36 weeks
Change in nutrient intake based on the recommended daily allowance (RDA)
기간: 12-24 weeks

Nutrient intake calculated from 3-day weighed food records and Food Frequency Questionnaire and Participant blood measurements of insulin, glucose, hemoglobin A1C, Vitamin K, homocysteine, lipids, fatty acid profile and vitamin D.

12-24 weeks
Change in nutrient intake based on the recommended daily allowance (RDA)
기간: 12-36 weeks

Nutrient intake calculated from 3-day weighed food records and Food Frequency Questionnaire and Participant blood measurements of insulin, glucose, hemoglobin A1C, Vitamin K, homocysteine, lipids, fatty acid profile and vitamin D.

12-36 weeks
Change in cognitive function
기간: 12-24 weeks

Symbol Digit Modalities Test - oral. An oral test of sequencing symbols. •Participant substitutes a number for meaningless geometric shapes based on a key that assigns a specific number to each shape. Scoring is based on the number of correct substitutions.

12-24 weeks
Change in cognitive function
기간: 12-36 weeks

Symbol Digit Modalities Test - oral. An oral test of sequencing symbols. •Participant substitutes a number for meaningless geometric shapes based on a key that assigns a specific number to each shape. Scoring is based on the number of correct substitutions.

12-36 weeks
Change in steps per day
기간: 12-24 weeks

Measured by accelerometer

12-24 weeks
Change in steps per day
기간: 12-36 weeks

Measured by accelerometer

12-36 weeks
Change in participant Quality of Life (QoL) - General Health
기간: 12-24 weeks

Multiple Sclerosis 54 Quality of Life Questionnaire. A series of questions about quality of life and social functioning. Score 0 to 100.

12-24 weeks
Change in participant Quality of Life (QoL) - General Health
기간: 12-36 weeks

Multiple Sclerosis Quality of Life Questionnaire. A series of questions about quality of life and social functioning. Score 0 to 100.

12-36 weeks
Change in participant Quality of Life (QoL) - Mental Health
기간: 12-24 weeks

Multiple Sclerosis Quality of Life Questionnaire A series of questions about quality of life and social functioning. Score 0 to 100.

12-24 weeks
Change in participant Quality of Life (QoL) - Mental Health
기간: 12-36 weeks

Multiple Sclerosis Quality of Life Questionnaire A series of questions about quality of life and social functioning. Score 0 to 100.

12-36 weeks
Change in total sleep time
기간: 12-24 weeks

Total sleep time is measured in hours and minutes and tracked by accelerometer worn by participants throughout the study

12-24 weeks
Change in total sleep time
기간: 12-36 weeks

Total sleep time is measured in hours and minutes and tracked by accelerometer worn by participants throughout the study

12-36 weeks
Change in perceived anxiety
기간: 12-24 weeks

Perceived anxiety is measured by the Hospital Anxiety and Depression Scale (HADS), a 14 question scale ranging from 0-3 with zero being being low or no occurrence and 3 being high occurrence.

12-24 weeks
Change in perceived anxiety
기간: 12-36 weeks

Perceived anxiety is measured by the Hospital Anxiety and Depression Scale (HADS), a 14 question scale ranging from 0-3 with zero being being low or no occurrence and 3 being high occurrence.

12-36 weeks
Change in perceived depression
기간: 12-24 weeks

Perceived depression is measured by the Hospital Anxiety and Depression Scale (HADS), a 14 question scale ranging from 0-3 with zero being being low or no occurrence and 3 being high occurrence.

12-24 weeks
Change in perceived depression
기간: 12-36 weeks

Perceived depression is measured by the Hospital Anxiety and Depression Scale (HADS), a 14 question scale ranging from 0-3 with zero being being low or no occurrence and 3 being high occurrence.

12-36 weeks

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

수사관

  • 수석 연구원: Terry L Wahls, MD, MBA, University of Iowa
  • 수석 연구원: Linda Snetselaar, PhD, RD,, University of Iowa

간행물 및 유용한 링크

연구에 대한 정보 입력을 담당하는 사람이 자발적으로 이러한 간행물을 제공합니다. 이것은 연구와 관련된 모든 것에 관한 것일 수 있습니다.

일반 간행물

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2016년 8월 1일

기본 완료 (실제)

2020년 1월 26일

연구 완료 (실제)

2025년 2월 26일

연구 등록 날짜

최초 제출

2016년 9월 13일

QC 기준을 충족하는 최초 제출

2016년 9월 22일

처음 게시됨 (추정된)

2016년 9월 26일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 9월 18일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 9월 15일

마지막으로 확인됨

2026년 9월 1일

추가 정보

이 연구와 관련된 용어

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

예

IPD 계획 설명

Scientists may request data for a PROSPERO registered meta-analysis that has been published in a peer reviewed journal.

IPD 공유 기간

One year after publication of data.

IPD 공유 액세스 기준

Scientists who have a PROSPERO registered meta-analysis with a protocol that has been published in a peer reviewed journal may request data for that meta-analysis. The scientist will use their academic email to reach out to the PI with the protocol manuscript describing the data that is requested, their address, phone number and contact details. Upon review of the documents, and the request, the PI will determine if the request meets guidelines. If the request is deemed appropriate the PI will initiate an outgoing material data use agreement with the Division of Sponsored Programs at the University of Iowa who will contact the requesting scientists to sign the contract.

IPD 공유 지원 정보 유형

  • 연구_프로토콜
  • ICF

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

구독하다