NCT07315789

Brief Summary

Sarcopenia is one of the main problems in the elderly population. The concept of disease has evolved, as have its treatment strategies. Among these is high-intensity interval training (HIIT). This approach has been little studied in older adults with sarcopenia, especially in institutionalized older adults in nursing homes. So this will be the objective of the study. A randomised clinical trial is being conducted to analyse how these diagnostic criteria for sarcopenia evolve after the application of HIIT compared to a control group.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
164

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Feb 2022

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

February 1, 2022

Completed
3.9 years until next milestone

First Submitted

Initial submission to the registry

December 10, 2025

Completed
5 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 15, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 15, 2025

Completed
18 days until next milestone

First Posted

Study publicly available on registry

January 2, 2026

Completed
Last Updated

March 17, 2026

Status Verified

March 1, 2026

Enrollment Period

3.9 years

First QC Date

December 10, 2025

Last Update Submit

March 14, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Hand grip strenght

    The researchers used the JAMAR dynamometer

    Thrice at the baseline: at the start, at 8 weeks and at 12 weeks.

Secondary Outcomes (3)

  • Muscular mass / appendicular skeletal mass (ASM)

    Thrice at the baseline: at the start, at 8 weeks and at 12 weeks.

  • Physical performance

    Thrice at the baseline: at the start, at 8 weeks and at 12 weeks.

  • Physical performance 2

    Thrice at the baseline: at the start, at 8 weeks and at 12 weeks.

Study Arms (2)

This group includes institutionalized older adults aged 60 and over for treatment.

EXPERIMENTAL
Other: High-intensity interval strength training: therapeutic exercise programme.

This group includes institutionalized older adults aged 60 and over.

NO INTERVENTION

Interventions

A 12-week high-intensity interval strenght training (HIITs) programme is developed with basic exercises adapted to the living environment of older people. Progress in the exercises over the twelve weeks is measured using the maximum weight that can be lifted in one repetition (1-RM), maximum heart rate (MHR) and the Borg scale.

This group includes institutionalized older adults aged 60 and over for treatment.

Eligibility Criteria

Age60 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • older adults who have been institutionalized for at least one year
  • older adults who are institutionalized with clinical suspicion of sarcopenia according to the Sarc-F questionnaire and muscle strength criteria
  • older adults residing in the community of Extremadura.

You may not qualify if:

  • present cognitive impairment (score \<24 Mini-Mental State Examination)
  • primary, serious, or chronic diseases that could explain the decrease in muscle strength and the other diagnostic variables of the participants
  • diseases or physical disorders that hinder the assessment of the participants; -use of drugs that may affect muscle strength and mass.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Universidad de Extremadura

Badajoz, Spain

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
QUADRUPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Clinical professor

Study Record Dates

First Submitted

December 10, 2025

First Posted

January 2, 2026

Study Start

February 1, 2022

Primary Completion

December 15, 2025

Study Completion

December 15, 2025

Last Updated

March 17, 2026

Record last verified: 2026-03

Locations