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Physical Activity, Nutrition and Health: Influence of a training and nutritional intervention on health-related parameters of yet physically inactive people

Physical Activity, Nutrition and Health: Influence of a training and nutritional intervention on health-related parameters of yet physically inactive people - BEGinn

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00014322
Enrollment
100
Registered
2018-03-28
Start date
2018-08-13
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Physical inactivity

Interventions

Group 1: Sports intervention: Includes the independent performance of a standardized fitness circle in cooperating fitness centers, twice a week for 12 weeks. Group 2: Sports and nutritional intervent

Sponsors

Institut für Lebensmittelwissenschaft und Humanernährung
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 70 Years

Inclusion criteria

Inclusion criteria: - consent men and women - 50 - 70 years - so far physically inactive people who have not carried out specific sports activities outside of their daily activities for at least 2 years - sports capability - willingness to independently perform a training program for 12 weeks - willingness to implement given dietary recommendations in everyday life - willingness to take a multivitamin mineral preperation daily for 12 weeks - willingness to be assigned to the waiting control group and to receive the intervention after a waiting period of 12 weeks - stable weight since min. half a year (± 5 kg) - omnivorous diet

Exclusion criteria

Exclusion criteria: - severe chronic diseases (cancer, type 1 diabetes, etc.), manifest cardiovascular diseases, renal insufficiency, liver disease - chronic diseases of the gastrointestinal tract (e.g., ulcerative colitis, Crohn's disease, pancreatic insufficiency) - blood coagulation disorders - known immunological disorders (e.g., autoimmune diseases) - regular intake of laxatives - permanent use of immunosuppressive drugs (cortisone, anti-inflammatory drugs, non-steroidal anti-inflammatory drugs, etc.) - drug, alcohol and medication abuse - non-consenting subjects - simultaneous participation in another clinical study or participation within the past 30 days - ingestion of mineral and / or vitamin supplements, unless discontinued 6-8 weeks prior to study

Design outcomes

Primary

MeasureTime frame
Determination of the CD4 / CD8 ratio of T-cells in venous blood at the beginning and at the end of the twelve-week intervention.

Secondary

MeasureTime frame
At the beginning and end of the intervention, the following parameters will be determined from venous blood: - i.a. immunological parameters, e.g. number of regulatory T-cells, T-cell apoptosis and activation markers (Annexin V and CD69) - i.a. biochemical parameters (e.g., parameters of iron metabolism, vitamin B12 (cobalamin)), - i.a. Health status survey (e.g., SF36) - i.a. Survey of diet and exercise behavior (e.g., FFQ, Freiburger Fragebogen questionnaire on physical activity) - anthropometric data

Countries

Germany

Contacts

Public ContactPaulina Wasserfurth

Institut für Lebensmittelwissenschaft und Humanernährung

wasserfurth@nutrition.uni-hannover.de0551 762 3733

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026