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NCT Number: NCT07205016

FreeFrail Project: A Multicomponent Intervention for the Management of Frailty in Primary Care: A Randomized Controlled Trial

The primary aim is to assess the effectiveness of a multicomponent intervention including dual-task exercise in improving functionality and cognitive performance and in reducing frailty among community-dwelling adults aged ≥65 years compared to usual care. Secondary objectives include evaluating its impact on pain, anxiety or depression, sleep quality, quality of life, physical activity, handgrip strength, and polypharmacy.

A double-blind, randomized, parallel-group controlled trial will be conducted in primary care centers in Lleida. Frail older adults (≥65 years) will be recruited and randomly allocated to either the intervention group, receiving a structured cognitive-motor dual-task based multicomponent program, or the control group, receiving usual care. Outcomes will be assessed using validated tools at baseline and follow-up.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 65 or older
  • Frailty according to Fragil-VIG index (>0,20)
  • Barthel index > 60
  • Able to perform physical exercise
  • Able to understand and communicate in Catalan or Spanish

Exclusion criteria

  • Decompensated / Unstable cardiovascular disease or recent diagnosed
  • Upper or lower injury with functional impairment
  • Institutionalized patient.
  • Terminal or tumoral processes
  • People who participated in another clinical trial or exercise programme during last year
  • Diagnosis of severe dementia

Treatment and study plan

Dual task exercise

Behavioral

The intervention group will conduct the same multicomponent intervention than the control group, but adding the dual cognitive task while performing the therapeutic physical activity, which may include counting numbers backwards, in 2s, mentioning names of animals, food, countries and others. The objective of this additional condition is to stimulate cognitive and functional capacity simultaneously, increasing the complexity of the activity and the transfer to daily life activities.

Otago exercise

Behavioral

The proposed intervention is a multicomponent program designed to address frailty in community-dwelling older adults. It integrates three evidence-based domains: therapeutic physical activity, cognitive psychological intervention, and nutritional support.

Primary outcomes

  1. Physical performance and functional status

    Time frame: From enrollment to the end of treatment at 12 weeks

    The Short Physical Performance Battery (SPPB) is an ordinal quantitative scale ranging from 0 to 12. This validated tool assesses three functional domains: lower-limb muscle strength, by timing the repeated chair-stand test; gait speed, through the 4-meter walking test; and static balance, evaluated with three progressively difficult positions (feet together, semi-tandem, tandem). A composite score is calculated, with lower values reflecting poorer performance. A score of 9 or less has been widely adopted as a cut-off point for identifying frailty and pre-frailty in older adults, making this instrument particularly suitable for evaluating the effectiveness of interventions on physical function

  2. Cognitive function

    Time frame: From enrollment to the end of treatment at 12 weeks

    The Mini-Mental State Examination (MMSE) is a continuous quantitative widely used 30-point screening tool validated for older adults to assess global cognitive function. It evaluates orientation, memory, attention, language, and praxis, providing a standardized quantitative measure of cognitive status. Although limited in sensitivity for mild or executive deficits, the MMSE remains a practical first-line assessment in frailty research and clinical protocols, and its integration alongside multidimensional frailty measures allows for a more comprehensive characterization of cognitive vulnerability in aging. A culturally adapted and validated version is available in Spanish, enabling its use in Hispanic populations.

  3. Frailty status

    Time frame: From enrollment to the end of treatment at 12 weeks

    The Frailty-VIG is an ordinal quantitative measure specifically validated for older adults in the community. This multidimensional tool comprises 22 dichotomous items spanning activities of daily living, nutrition, cognition, emotional health, social context, geriatric syndromes, and chronic diseases. By incorporating multimorbidity and psychosocial domains alongside physical aspects, the Frailty-VIG provides a comprehensive assessment of frailty, overcoming the limitations of purely physical indices

Secondary outcomes

  1. Quality of life / Anxiety and Depression / Pain severity

    Time frame: From enrollment to the end of treatment at 12 weeks

    will be evaluated with the EuroQoL-5D-5L which generates ordinal categorical variables from five dimensions of health: mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each dimension is rated on a five-point Likert scale, where higher scores denote lower quality of life. This standardized and validated instrument has been extensively applied in Spanish populations and is particularly appropriate to capture the multidimensional impact of frailty on health-related quality of life

  2. Sleep performance

    Time frame: From enrollment to the end of treatment at 12 weeks

    will be assessed using the Spanish validated version of the Pittsburgh Sleep Quality Index (PSQI). This self-administered questionnaire yields a global score between 0 and 21, with higher scores reflecting worse sleep quality. It evaluates seven components-subjective quality, latency, duration, habitual efficiency, disturbances, medication use, and daytime dysfunction. A score above 5 is commonly considered indicative of clinically relevant sleep impairment. As poor sleep has been consistently associated with frailty and functional decline, the PSQI offers a sensitive and appropriate measure for this study

  3. Physical activity

    Time frame: From enrollment to the end of treatment at 12 weeks

    will be assessed through the International Physical Activity Questionnaire (IPAQ), which produces continuous quantitative data expressed in metabolic equivalent task minutes per week (MET-min/week). It includes seven open questions regarding activity over the previous seven days, covering walking, moderate and vigorous activities, and sedentary behaviour. The calculation of MET-min/week allows standardized estimation of global activity levels. This questionnaire is validated and widely used in community-dwelling adults, making it an appropriate measure for capturing the impact of the intervention on activity levels

  4. Handgrip strength

    Time frame: From enrollment to the end of treatment at 12 weeks

    will be measured with a handheld dynamometer. Results are expressed as continuous quantitative variables in kilograms. Following standardized protocols, participants will be seated with the elbow flexed at 90° and the wrist positioned between neutral and 30° dorsiflexion. They will be instructed to squeeze the dynamometer maximally for 3-5 seconds. Three trials will be performed alternately in each hand, with one-minute rest intervals, and the best value will be recorded. Handgrip strength is a simple, reliable, and validated marker of sarcopenia and frailty risk, strongly correlated with morbidity and mortality in older adults

  5. Inflammatory and mitochondrial function biomarkers

    Time frame: From enrollment to the end of treatment at 12 weeks

    are strongly supported by the literature in frail population, as these biological factors are fundamentally implicated in the pathways leading to frailty, sarcopenia, and functional impairment. Chronic low-grade inflammation ("inflammaging"), a hallmark of aging, is characterized by increased levels of circulating pro-inflammatory cytokines such as interleukin 6 and 8(IL-6, IL-8), interleukin 1β (IL-1β), tumor necrosis factor-α (TNF-α), and C-reactive protein (CRP). These biomarkers consistently correlate with chronic low-grade inflammation ("inflammaging") and mitochondrial dysfunction (3) they have also been consistently associated with sarcopenia, frailty, and functional decline (4,5) . The blood samples will be analysed at Biomedical Research Institute of Lleida (IRB Lleida), generating continuous quantitative data.

Study contacts

Contact information is provided by the study sponsor or research team.

Oriol Martínez-Navarro, Doctor

CONTACT

[email protected]

619562618

Sponsors and collaborators

Lead sponsor

Universitat de Lleida

Other

Collaborators

  • Institut Catala de Salut

Registry information

Official study title

FreeFrail Project: Effectiveness of a Multicomponent Intervention Including Dual-task Exercise to Increase Functionality and Cognitive Performance in Frail and Pre-frail Individuals Over 65 Years Aged in Primary Care Compared to Usual Care: Protocol for a Randomized Controlled Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Oct 3, 2025
Registry last updated
Oct 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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