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Changes in Everyday Life After a Tai Chi or Eurythmy Intervention in Elderly People at Risk of Falling: a Qualitative Exploration as a Sub-Study of the ENTAiER Study

NCT05547178 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 16

Last updated 2024-01-19

No results posted yet for this study

Summary

The ENTAiER fall prevention study investigates the efficacy and safety of eurythmy therapy and tai chi in older people with chronic diseases and an increased risk of falls. In the course of the ENTAiER study, the participants observed changes in themselves and in their everyday life and described them in conversation, which could not be recorded with the research methods used. A qualitative exploration of these subjectively experienced changes among participants of the ENTAiER study will be conducted as part of a sub-study. For this purpose, group interviews will be conducted.

Conditions

  • Increased Risk of Falls

Interventions

OTHER

Qualitative interview - eurythmy group

Participants will be interviewed about self-perceived changes in everyday life during participation in the eurythmy intervention of the ENTAiER study.

OTHER

Qualitative interview - tai chi group

Participants will be interviewed about self-perceived changes in everyday life during participation in the tai chi intervention of the ENTAiER study.

OTHER

Qualitative interview - standard care group

Participants will be interviewed about self-perceived changes in everyday life during participation in the standard care group of the ENTAiER study.

Sponsors & Collaborators

  • ARCIM Institute Academic Research in Complementary and Integrative Medicine

    lead OTHER

Principal Investigators

  • Jan Vagedes, Dr · ARCIM Institute

Eligibility

Min Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-11-09
Primary Completion
2023-10-16
Completion
2023-10-16

Countries

  • Germany

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05547178 on ClinicalTrials.gov