The Effect on Function of Increasing Activity for Nursing Home Residents

This study has been completed.
Sponsor:
Collaborator:
Helse Midt-Norge
Information provided by (Responsible Party):
Norwegian University of Science and Technology
ClinicalTrials.gov Identifier:
NCT00218842
First received: September 20, 2005
Last updated: March 6, 2014
Last verified: March 2014
  Purpose

As designs of existing outcome studies are disparate and do not always relate well to a Swedish context, the need for further studies is obvious. Also, an empirical theory drawn from the best practice supporting autonomy and wellbeing for clients in a nursing home setting has not yet been fully depicted. The study described below intends to fill a gap in knowledge related to the effect of enhanced activities of daily living (ADL)-training, physical, and daily activities and staff education in a nursing home setting, based on a theory- and evidence-based intervention programme in a Swedish as well as a Nordic health care context. The aims of the study are to describe the impact of an individually tailored intervention program, in a nursing home setting, on:

  • Physical capacity
  • Degree of dependence in ADL
  • Long-term participation in physical and/or daily activities
  • Self-rated wellbeing

Condition Intervention
Frailty
Nursing Home Residents
Behavioral: Individualized exercise

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Treatment
Official Title: Physical and Daily Activity for Residents in a Nursing Home Setting. -A Nordic Multi-Centre Study

Resource links provided by NLM:


Further study details as provided by Norwegian University of Science and Technology:

Primary Outcome Measures:
  • Physical function [ Time Frame: baseline, three and six months ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Falls [ Time Frame: during six months ] [ Designated as safety issue: No ]

Enrollment: 125
Study Start Date: October 2005
Study Completion Date: December 2009
Primary Completion Date: October 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: exercise group
individualized exercise
Behavioral: Individualized exercise
individualized exercise, physical activity and training in daily life situations given by trained physical therapists and occupational therapists
No Intervention: control group
care as usal

Detailed Description:

The Trondheim study has additional aims to assess the impact of intervention on:

  • Urinary incontinence
  • Falls
  Eligibility

Ages Eligible for Study:   65 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • > 65 years of age
  • Expected stay in the nursing home > 3 months
  • Able to take instruction

Exclusion Criteria:

  • Persons in a terminal phase
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT00218842

Locations
Norway
Section of Geriatric Medicine, St. Olavs University Hospital
Trondheim, Norway, N-7016
Sponsors and Collaborators
Norwegian University of Science and Technology
Helse Midt-Norge
Investigators
Study Chair: Jorunn L Helbostad, PhD St. Olavs University Hospital and Norwegian University of Science and Technology