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N/A N=9 Randomized Supportive Care

Strength on Wheels: A Meal Delivery and Exercise Intervention for Homebound Older Adults

Frailty

Enrolled (actual)
9
Serious AEs
22.2%
Results posted
Jul 2021
Primary outcome: Primary: Overall Frailty Status as Assessed by the Fried Frailty Phenotype (FFP) Screening Test. — 2; 2; 2; 3 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Meals plus exercise (Behavioral); Meals only (Behavioral)
Age
Adult, Older Adult · 60+ yrs
Sex
All
Sponsor
The University of Texas Health Science Center, Houston
Primary completion
Jan 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Overall Frailty Status as Assessed by the Fried Frailty Phenotype (FFP) Screening Test.
2; 1; 2; 4; 0; 0
PRIMARY
Overall Frailty Status as Assessed by the Fried Frailty Phenotype (FFP) Screening Test.
2; 1; 2; 4; 0; 0
SECONDARY
Levels of Plasma Vitamin C
3738.89; 2055.56
SECONDARY
Levels of Plasma Vitamin C
3738.89; 2055.56
SECONDARY
Levels of Serum Folate
19.56; 10.85
SECONDARY
Levels of Serum Folate
19.56; 10.85
SECONDARY
Levels of Vitamin B12
875.42; 528.44
SECONDARY
Levels of Vitamin B12
875.42; 528.44
SECONDARY
Levels of Vitamin 25-OHD
126.72; 61.68
SECONDARY
Levels of Vitamin 25-OHD
126.72; 61.68
SECONDARY
Levels of Methylmalonic Acid (MMA)
554.55; 388.75
SECONDARY
Levels of Methylmalonic Acid (MMA)
554.55; 388.75
SECONDARY
Levels of Homocysteine (HCy)
18.83; 21.24
SECONDARY
Levels of Homocysteine (HCy)
18.83; 21.24

Summary

The purpose of this study is to implement a home-based exercise program, administered through Interfaith Ministries of Greater Houston Meals on Wheels (MOWGH), and evaluate its effects on frailty status and nutritional markers in homebound older adults.

Eligibility Criteria

Inclusion Criteria

  • enrolled in UT-Health Harris Health House Call Program (HCP)
  • Frail or pre frail by FFP
  • medically stable

Exclusion Criteria

  • robust by FFP
  • Mini-Cog score <3 and/or are unable to follow instructions
  • pre-diagnosed terminal illness
  • unable to ambulate, and/or are unable to use their upper extremities
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04087343). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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