EXDES: Effects of 12-week Exercise Program on Sleep Quality and Fear of Death in Geriatric Individuals

Sponsor
Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey (Other)
Overall Status
Recruiting
CT.gov ID
NCT05418283
Collaborator
(none)
60
1
2
5.7
10.6

Study Details

Study Description

Brief Summary

The aim of this study is to determine the effect of regular aerobic exercise program on tanatophobia and sleep quality in elderly individuals, and to evaluate the relationship between sleep disorder and fear of death.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Exercise
N/A

Detailed Description

The effect of regular exercise programs on fear of death in elderly individuals is unknown. The aim of this study is to determine the effect of regular aerobic exercise program on tanatophobia and sleep quality in elderly individuals, and to evaluate the relationship between sleep disorder and fear of death.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effects of 12-week Exercise Program on Sleep Quality and Fear of Death in Geriatric Individuals
Actual Study Start Date :
Jun 10, 2022
Anticipated Primary Completion Date :
Nov 30, 2022
Anticipated Study Completion Date :
Nov 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Exercise

12-week aerobic exercise program will be applied (3/week)

Behavioral: Exercise
1 hour of aerobic exercise will be applied 3 days a week for 12 weeks.

No Intervention: Control

No intervention will be applied.

Outcome Measures

Primary Outcome Measures

  1. thanatophobia [1 week]

    evaluation of thanatophobia

Secondary Outcome Measures

  1. sleep quality [1 week]

    evaluation of sleep quality

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Individuals aged 65 and over who volunteered to participate in the study,

  • Conscious and without communication problems,

  • No orthopedic injury that prevents walking

  • Those who are physically inactive according to the International Physical Activity Assessment Questionnaire

  • Those who have sufficient motivation to participate in the exercise program (will be evaluated by a one-on-one interview by the researchers)

  • Being eligible to participate in an exercise program after a cardiac examination by a cardiologist (resting ECG and questioning of cardiac symptoms, further examinations such as exercise ECG test if necessary)

Exclusion Criteria:
  • Having a history of neuromuscular disease

  • Serious medical condition (eg advanced malignancy or major neurological, psychiatric or endocrine disease, respiratory failure, etc.) that would prevent the person from participating in exercise training.

  • Less than 1 year life expectancy

  • Having an orthopedic injury that prevents walking

  • Presence of advanced sensory deficit

  • Having visual and hearing problems

  • Not having sufficient communication skills (Mini Mental Test score below 24 points)

  • Not having agreed to participate in the study

  • Uncontrolled hypertension

  • Not being found suitable for exercise in the examination performed by physicians and physiotherapists

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sultan Abdülhamid Training and Research Hospital Üsküdar İstanbul Turkey 34660

Sponsors and Collaborators

  • Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

Investigators

  • Principal Investigator: Elif Yıldırım Ayaz, M.D., Sultan Abdülhamid Training And Research Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey
ClinicalTrials.gov Identifier:
NCT05418283
Other Study ID Numbers:
  • EXDES
First Posted:
Jun 14, 2022
Last Update Posted:
Aug 25, 2022
Last Verified:
Aug 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 25, 2022