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Effects of Fasting on Self Efficacy

Completed
Conditions
Cardiovascular Diseases
Fibromyalgia
Gout
Irritable Bowel Syndrome
Inflammatory Bowel Disease
Rheumatoid Arthritis
Arthritis
Gastrointestinal Diseases
Chronic Pain
Headache
Interventions
Behavioral: Fasting
Registration Number
NCT02113111
Lead Sponsor
Universität Duisburg-Essen
Brief Summary

The study aims to investigate

* if a 7 day therapeutic fasting regimen will affect self-efficacy of patients with chronic diseases

* the effects of fasting on physical and mental well-being, quality of life and body awareness/image

* the association between patients characteristics and the perceived health benefit after fasting

* the association between Diagnosis according to traditional Chinese medicine and physical and mental well-being during the course of fasting

* experiences and perceptions of patients during fasting therapy

Detailed Description

see above

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
120
Inclusion Criteria
  • 18 years or older
  • eligible for fasting, i.e. normal weight (no anorexia, no nutritional deficiency, no BMI<18 or >35, no eating disorder)
Exclusion Criteria
  • psychiatric disorder
  • type 1 diabetes
  • hepatitis
  • severe somatic disorder (oncological disease, hepatological or nephrological)
  • pregnancy

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
FastingFastingPatients being admitted to an internal integrative medicine hospital and referred to therapeutic fasting therapy
Primary Outcome Measures
NameTimeMethod
Bodily self-efficacyup to 6 months

Bodily self-efficacy (Schützler and Witt, 2013)

Self efficacy questionnaireup to 6 months

Self efficacy questionnaire (SWE) by Schwarzer and Jerusalem, 1999

Secondary Outcome Measures
NameTimeMethod
Health-related quality of life2 weeks, 6 months

Short Form (36) Health Survey

Depression2 weeks, 6 months

Becks Depression Inventory (BDI)

Easiness of life2 weeks, 6 months

Questionnaire on emotional and physical reactions

Body awareness and dissociation2 weeks, 6 months

Scale of Body Connection (SBC) (Price and Thompson 2007)

Symptoms2 weeks, 6 months

MYMOP questionnaire (Paterson)

Ability and will to change2 weeks, 6 months

Ability and will to change (Büssing, 2008)

Body Awareness2 weeks, 6 months

Body Awareness Questionnaire (BAQ) (Shields 1989)

Body responsiveness2 weeks, 6 months

Body Responsiveness Scale (BRS)(Daubenmier 2005)

Safety2 weeks

Any adverse effect during the study period

Trial Locations

Locations (1)

Department of Internal and Integrative Medicine, Kliniken Essen-Mitte

🇩🇪

Essen, Germany

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