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临床试验/NCT04303260
NCT04303260已完成不适用

Special Physical Exercises as a Therapeutic Intervention for Inflammatory Bowel Disease

Tel-Aviv Sourasky Medical Center1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2019年7月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
36
试验地点
1
主要终点
Clinical response as assessed by a change in PROMIS questionnaire

研究概览

简要总结

The investigator is hypothesize that physical activity can have positive effects on health, general well-being , sleep quality and stress in Inflammatory Bowel Disease patients.

详细描述

A randomized-controlled-double blinded pilot study. 50 Inflammatory Bowel Disease patients, suffering from mild disease will be randomized to undergo either a set of specific physical exercises for Inflammatory Bowel Disease or a control set of unrelated exercises.

Patients will be randomized to either interventional or control groups by a computer automatized randomization program. Patients will be sent an email with the link to an internet site where they will be able to watch the exercise program.

The interventional exercise regimen will include specific exercises postulated to increase blood flow to the intestine and colon and thereby promote normal peristaltic and decrease inflammation. The control arm will practice generally recommended exercises, without particular attention to the abdomen.

Videos of sets of exercise will be available online which patients will be able to watch and follow from their home computer. The exercise regimens (both interventional and controls) will be sequenced and performed by a trained and experienced instructor, which will provide these to the PI. Each video will include explicit instructions and examples for each of the exercises. Patients will be asked to watch the videos and preform the exercises individually every day. Patients in the interventional arm will be asked to complete 3 different videos repeatedly, as many days a week sets as possible. This repetition is to be maintained even if a patient missed one day of training to perform sets of 15 minutes/ day, 6 times a week.; Compliance will be documented by patients through emails to the study coordinator. Patients in the controled arm will also be asked to practice generally recommended exercises in 3 different videos repeatedly, as many sets as possible.

Patients will answer questionnaires once every two weeks(week 0, 2, 4). Patients will answer QOL(quality of life), PROMs(Patient Reported Outcome Measures),disease activity , Sleep questionnaire and Morningness eveningness questionnaire. Also, before and after the intervention (week 0 and week 4) patients will visit the clinic for anthropometric measurements and to give serum, stool and urine sample which will be analyzed for inflammatory markers, microbial composition and function.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • 18 < age < 60
  • Clinically stable patients, constant medicinal regimen throughout the study period. Refractory to mesalamine at least 6 weeks, or steroids at least 2 week, or immunomodulator at least 12 weeks or biologics at least 12 weeks therapy, medical cannabis at least 2 weeks before the study.
  • CD patients will be included if their symptoms score 5≤ between ≤15 on the Harvey-Bradshaw index (HBI) score
  • UC patients will be included if their symptoms score 3≤between≤9 on the Simple Clinical Colitis Activity Index (SCCAI)

排除标准

  • Inability to commit for performing at least 15 minutes of exercise, 6 times a week
  • Lack of availability or capability to use a computer/ internet.
  • Any proven current infection such as Clostridium difficile infection, positive stool culture, or parasites.
  • Inability to sign informed consent and complete study protocol
  • Subjects with chronic conditions such as cancer, organ transplant subjects, advanced kidney or liver disease, systemic inflammatory conditions other than IBD.
  • Patients with ileostomy, pouch or short bowel

结局指标

主要结局

Clinical response as assessed by a change in PROMIS questionnaire

时间窗: After 4 weeks

PROMIS (Patient-Reported Outcomes Measurement Information System)

Clinical response as assessed by a change in SCCAI

时间窗: After 4 weeks

Doctor evaluation- Simple Clinical Colitis Activity Index Bowel frequency (day): * 0-3 / day (0) * 4-6 / day (1) * 7-9 / day (2) * \>9 / day (3) Bowel frequency (night): * 0 / night (0) * 1-3 / night (1) * 4-6 / night (2) General well being: * very well (0) * slightly below par (1) * poor (2) * very poor (3) * terrible (4) Urgency of defecation: * none (0) * Hurry (1) * Immediately (toilet nearby) (2) * Incontinence (3) Blood in stool: * None (0) * Trace (1) * Occasionally (\<50% of defecations) (2) * Usually (\>50% of defecations) (3) SCCAI Score: (add scores of questions 1 to 5) Remission\<3 Mild Disease 3-5 Moderate Disease 6-9 Severe Disease ≥10

Clinical response as assessed by a change in QOL questionnaire

时间窗: After 4 weeks

Quality of life questionnaire

Clinical response assessed by a change in HBI

时间窗: After 4 weeks

Doctor evaluation -The Harvey-Bradshaw index activity index Harvey Bradshaw Index (based on the day before): General well-being: * very well =0 * slightly below par =1 * poor =2 * very poor =3 * terrible =4 Abdominal pain: * none =0 * mild =1 * moderate =2 * severe =3 Abdominal mass: * none =0 * dubious =1 * definite =2 * definite and tender =3 Number of liquid stools per day: Complications: * none =0 * arthralgia =1 * uveitis =1 * erythema nodosum =1 * aphthous ulcers =1 * pyoderma gangrenosum =1 * anal fissure =1 * new fistula =1 * abscess =1 SCORE: \<5 Remission 5-7 Mild activity 8-16 Moderate activity \>16 Sever activity

次要结局

未报告次要终点

研究者

申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Shmuel Kivity, MD

Director of Clinical Research and Development Department

Tel-Aviv Sourasky Medical Center

研究点 (1)

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