BASIC: Balance Training for Elders With Heart Failure

Sponsor
University of Nebraska (Other)
Overall Status
Completed
CT.gov ID
NCT02566785
Collaborator
American Nurses Foundation (Other)
33
1
2
10.5
3.1

Study Details

Study Description

Brief Summary

Purpose: The purpose of this pilot study is to evaluate the effect of a multi-component balance & resistance training [RT] intervention on physical function, balance, & falls in older [≥ 65 y/o] community dwelling heart failure [HF] patients. The study aims: 1] Pilot test multi-component balance activities & RT intervention on primary outcomes. 2] Explore perceptions related to outcomes & the intervention through focus groups. 3] Generate pilot data on adherence. 4] Generate pilot data on feasibility of conducting the BASIC Training intervention.

Background/Significance: Falls are the leading cause of injury-related deaths in this group. Fall risks are even greater for those with HF due to decreased exercise capacity, loss of skeletal muscle & medication side effects. Though RT is effective for improving skeletal muscle, it has only a modest effect on improving balance, which is comprised of peripheral sensory input central integration, & motor output. A multi-component intervention focusing on balance retraining & strengthening the muscles supporting static/dynamic balance & functional mobility is necessary.

Methods: Design - Randomized, two-group with wait list control, repeated measures experimental design. Sample/ Setting - 40-50 participants recruited from medical center heart failure clinic; supervised group sessions conducted in center's health & wellness center. Procedures - Participants will be randomized to intervention group or wait list control group. Focus groups pre/post intervention. The intervention will be administered in 1x per week supervised group sessions & 2x a week home sessions. Instruments - 30 Second Sit-to-St&, Modified Clinical Test of Sensory Interaction on Balance, Activity Specific Balance Confidence Scale, Timed Up & Go, Dynamic Gait Index.

Analysis Plan: Aim 1- independent t-test to compare change scores from baseline to the end of the first 12 week period for the intervention group with the wait list control group. A second analysis will combine data from the delayed intervention period for the wait list control group with that from the first 12 week period for the intervention group to test change. Supplemental analysis, involving only data from intervention group, will test whether change is sustained at 24 weeks. Aim 2 - thematic analysis conducted with focus group data. Aim 3 - adherence assessed by group session attendance & home activities completed. Aim 4 - assess & report logistics of conducting the study.

Nursing Relevance/Implications: This pilot study will initiate the process of developing a targeted intervention to induce changes in elderly HF patients to prevent future falls; thus reducing costs, physical & emotional burdens related to falls; & effect a major difference in the quality of life for this population.

Condition or Disease Intervention/Treatment Phase
  • Other: Balance Intervention
N/A

Detailed Description

Purpose: The purpose of this pilot study is to evaluate the effect of a multi-component balance and resistance training [RT] intervention on physical function, balance, and falls in older [≥ 65 y/o] community dwelling heart failure [HF] patients. The study aims: 1] Pilot test multi-component balance activities and RT intervention on primary outcomes. 2] Explore perceptions related to outcomes and the intervention through focus groups. 3] Generate pilot data on adherence. 4] Generate pilot data on feasibility of conducting the BASIC Training intervention.

Background/Significance: Falls are the leading cause of injury-related deaths in this age group. Fall risks are even greater for those with HF due to decreased exercise capacity, loss of skeletal muscle and medication side effects. Though RT is effective for improving skeletal muscle, it has only a modest effect on improving balance, which is comprised of peripheral sensory input central integration, and motor output. A multi-component intervention focusing on balance retraining and strengthening the muscles supporting static/dynamic balance and functional mobility is necessary.

Methods: Design - Randomized, two-group with wait list control, repeated measures experimental design. Sample/ Setting - 40-50 participants recruited from a medical center heart failure clinic; supervised group sessions conducted in the center's health and wellness center. Procedures - Participants will be randomized to the intervention group or the wait list control group. Focus groups pre/post intervention. The intervention will be administered in 1x per week supervised group sessions and 2x a week home sessions. Instruments - 30 Second Sit-to-Stand, Modified Clinical Test of Sensory Interaction on Balance, Activity Specific Balance Confidence Scale, Timed Up and Go, Dynamic Gait Index.

Analysis Plan: Aim 1- independent t-test to compare change scores from baseline to the end of the first 12 week period for the intervention group with the wait list control group. A second analysis will combine data from the delayed intervention period for the wait list control group with that from the first 12 week period for the intervention group to test change. Supplemental analysis, involving only data from intervention group, will test whether change is sustained at 24 weeks. Aim 2 - thematic analysis conducted with focus group data. Aim 3 - adherence assessed by group session attendance and home activities completed. Aim 4 - assess and report logistics of conducting the study.

Nursing Relevance/Implications: This pilot study will initiate the process of developing a targeted intervention to induce changes in elderly HF patients to prevent future falls; thus reducing costs, physical and emotional burdens related to falls; and effect a major difference in the quality of life for this population.

Study Design

Study Type:
Interventional
Actual Enrollment :
33 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Balance Activities and Strengthening to Improve Condition [BASIC]: Training for Elders With Heart Failure
Study Start Date :
Feb 1, 2016
Actual Primary Completion Date :
Dec 16, 2016
Actual Study Completion Date :
Dec 16, 2016

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention Group

Those allocated to the intervention group will participate in a supervised group session exercise one time per week and be asked to exercise two more times per week at home.

Other: Balance Intervention
The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance.

Other: Wait List Control Group

The wait list control group will not participate in the intervention and will be asked to continue their usual activity level during the first 12 weeks and will receive the multi-component balance intervention during weeks 12-24.

Other: Balance Intervention
The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance.

Outcome Measures

Primary Outcome Measures

  1. Pre/Post Scores on the 30 Second Sit to Stand Test Will be Used to Detect Any Changes in Leg Strength and Endurance That Occur During the 12 Week Group Exercise Sessions. [Baseline and 12 weeks]

  2. Dynamic Gait Index [Baseline and 12 weeks]

    8 increasingly challenging walking tasks (normal gait speed, changes in gait speed, walking with horizontal and vertical head movements, walking with pivot turn, walking over and around obstacles and stair climbing). A walkway path measured at 20 feet was used. A research assistance observed and scored all participants using a 0-3 scale, 0 = severe gait impairment, 1 = moderate gait impairment, 2 = mild/minimal impairment, 3 = normal gait, with a total possible scale range of 0 to 24 points. Scores ≤ 19 points was used to classify falling risk (Shumway-Cook et al. 1997).

Secondary Outcome Measures

  1. Activity Balance Confidence Scale [Baseline and 12 weeks]

    Total range = 0-100% Higher values represent better outcome Total score is averaged = total%/16 responses

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • 65 years of age or greater;

  • New York Heart Association class II and III,

  • community dwelling;

  • able to speak and read English,

  • must have written permission from cardiologist to participate.

Exclusion Criteria:
  • wheel chair dependency;

  • history of significant residual neurologic deficits [e.g.: recent stroke];

  • recent history of whiplash or concurrent complaints of neck pain;

  • recent fracture or lower extremity surgery. Participants will be screened for cognitive dysfunction and must pass the Mini-Mental State Examination [with a score at or above 23 points].

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Nebraska Medical Center College of Nursing Lincoln Nebraska United States 68588-0220

Sponsors and Collaborators

  • University of Nebraska
  • American Nurses Foundation

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Rita L. McGuire, PhD, RN, Principal Investigator, University of Nebraska
ClinicalTrials.gov Identifier:
NCT02566785
Other Study ID Numbers:
  • 677-15-FB
First Posted:
Oct 2, 2015
Last Update Posted:
Oct 9, 2018
Last Verified:
Jul 1, 2017
Additional relevant MeSH terms:

Study Results

Participant Flow

Recruitment Details November 2015 through June 2016 at the Heart Failure Improvement Program of a regional hospital.
Pre-assignment Detail
Arm/Group Title Intervention Group Wait List Control Group
Arm/Group Description Those allocated to the intervention group will participate in a supervised group session exercise one time per week and be asked to exercise two more times per week at home. Balance Intervention: The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance. The wait list control group will not participate in the intervention and will be asked to continue their usual activity level during the first 12 weeks and will receive the multi-component balance intervention during weeks 12-24. Balance Intervention: The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance.
Period Title: Overall Study
STARTED 15 18
COMPLETED 14 15
NOT COMPLETED 1 3

Baseline Characteristics

Arm/Group Title Intervention Group Wait List Control Group Total
Arm/Group Description Those allocated to the intervention group will participate in a supervised group session exercise one time per week and be asked to exercise two more times per week at home. Balance Intervention: The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance. The wait list control group will not participate in the intervention and will be asked to continue their usual activity level during the first 12 weeks and will receive the multi-component balance intervention during weeks 12-24. Balance Intervention: The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance. Total of all reporting groups
Overall Participants 15 18 33
Age (Count of Participants)
<=18 years
0
0%
0
0%
0
0%
Between 18 and 65 years
0
0%
0
0%
0
0%
>=65 years
15
100%
18
100%
33
100%
Sex: Female, Male (Count of Participants)
Female
8
53.3%
8
44.4%
16
48.5%
Male
7
46.7%
10
55.6%
17
51.5%
Race (NIH/OMB) (Count of Participants)
American Indian or Alaska Native
0
0%
0
0%
0
0%
Asian
0
0%
0
0%
0
0%
Native Hawaiian or Other Pacific Islander
0
0%
0
0%
0
0%
Black or African American
0
0%
0
0%
0
0%
White
15
100%
18
100%
33
100%
More than one race
0
0%
0
0%
0
0%
Unknown or Not Reported
0
0%
0
0%
0
0%
Region of Enrollment (Count of Participants)
United States
15
100%
18
100%
33
100%

Outcome Measures

1. Primary Outcome
Title Pre/Post Scores on the 30 Second Sit to Stand Test Will be Used to Detect Any Changes in Leg Strength and Endurance That Occur During the 12 Week Group Exercise Sessions.
Description
Time Frame Baseline and 12 weeks

Outcome Measure Data

Analysis Population Description
Two of the participants in the WLC group were there for testing at 12 weeks.
Arm/Group Title Intervention Group Wait List Control Group
Arm/Group Description Those allocated to the intervention group will participate in a supervised group session exercise one time per week and be asked to exercise two more times per week at home. Balance Intervention: The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance. The wait list control group will not participate in the intervention and will be asked to continue their usual activity level during the first 12 weeks and will receive the multi-component balance intervention during weeks 12-24. Balance Intervention: The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance.
Measure Participants 14 13
Baseline
6.9
(4.2)
6.5
(3.6)
12 Weeks
7.9
(4.5)
7.7
(5.4)
2. Primary Outcome
Title Dynamic Gait Index
Description 8 increasingly challenging walking tasks (normal gait speed, changes in gait speed, walking with horizontal and vertical head movements, walking with pivot turn, walking over and around obstacles and stair climbing). A walkway path measured at 20 feet was used. A research assistance observed and scored all participants using a 0-3 scale, 0 = severe gait impairment, 1 = moderate gait impairment, 2 = mild/minimal impairment, 3 = normal gait, with a total possible scale range of 0 to 24 points. Scores ≤ 19 points was used to classify falling risk (Shumway-Cook et al. 1997).
Time Frame Baseline and 12 weeks

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Intervention Group Wait List Control Group
Arm/Group Description Those allocated to the intervention group will participate in a supervised group session exercise one time per week and be asked to exercise two more times per week at home. Balance Intervention: The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance. The wait list control group will not participate in the intervention and will be asked to continue their usual activity level during the first 12 weeks and will receive the multi-component balance intervention during weeks 12-24. Balance Intervention: The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance.
Measure Participants 14 15
Baseline
18.9
(3.8)
19.1
(4.6)
12 Weeks
20.9
(1.8)
18.9
(4.4)
3. Secondary Outcome
Title Activity Balance Confidence Scale
Description Total range = 0-100% Higher values represent better outcome Total score is averaged = total%/16 responses
Time Frame Baseline and 12 weeks

Outcome Measure Data

Analysis Population Description
[Not Specified]
Arm/Group Title Intervention Group Wait List Control Group
Arm/Group Description Those allocated to the intervention group will participate in a supervised group session exercise one time per week and be asked to exercise two more times per week at home. Balance Intervention: The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance. The wait list control group will not participate in the intervention and will be asked to continue their usual activity level during the first 12 weeks and will receive the multi-component balance intervention during weeks 12-24. Balance Intervention: The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance.
Measure Participants 14 15
Baseline
74.9
(17.3)
74.1
(12.6)
12 weeks
72.1
(13.3)
71.2
(15.8)

Adverse Events

Time Frame One year
Adverse Event Reporting Description
Arm/Group Title Intervention Group Wait List Control Group
Arm/Group Description Those allocated to the intervention group will participate in a supervised group session exercise one time per week and be asked to exercise two more times per week at home. Balance Intervention: The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance. The wait list control group will not participate in the intervention and will be asked to continue their usual activity level during the first 12 weeks and will receive the multi-component balance intervention during weeks 12-24. Balance Intervention: The multi-component balance intervention will be 1x per week in supervised group sessions and 2x a week sessions at home. Sessions will begin with a 5 minute warm up of major muscle groups using flexibility exercises and end with a cool down. Sessions will focus on improving static balance in the initial stages, then progress to dynamic balance.
All Cause Mortality
Intervention Group Wait List Control Group
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/15 (0%) 0/18 (0%)
Serious Adverse Events
Intervention Group Wait List Control Group
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 0/15 (0%) 0/18 (0%)
Other (Not Including Serious) Adverse Events
Intervention Group Wait List Control Group
Affected / at Risk (%) # Events Affected / at Risk (%) # Events
Total 1/15 (6.7%) 0/18 (0%)
Musculoskeletal and connective tissue disorders
Fall from chair to knee 1/15 (6.7%) 1 0/18 (0%) 0

Limitations/Caveats

[Not Specified]

More Information

Certain Agreements

Principal Investigators are NOT employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.

Results Point of Contact

Name/Title Dr. Rita McGuire
Organization University of Nebraska Medical Center College of Nursing
Phone 402-472-4712
Email rita.mcguire@unmc.edu
Responsible Party:
Rita L. McGuire, PhD, RN, Principal Investigator, University of Nebraska
ClinicalTrials.gov Identifier:
NCT02566785
Other Study ID Numbers:
  • 677-15-FB
First Posted:
Oct 2, 2015
Last Update Posted:
Oct 9, 2018
Last Verified:
Jul 1, 2017